NPHC 10-Q
Nutra Pharma Corp (NPHC)
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM
(Mark One)
| QUARTERLY REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934. |
For
the quarterly period ended
| TRANSITION REPORT UNDER SECTION 13 OR 15(d) OF THE EXCHANGE ACT |
For the transition period from _________ to ________
Commission
file numbers
(Name of registrant as specified in its charter)
(State or Other Jurisdiction of Organization) |
(IRS Employer Identification Number) |
| (Address of principal executive offices) | (Zip Code) |
(Registrant’s telephone number, including area code)
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class | Ticker symbol(s) | Name of each exchange on which registered | ||
| N/A | N/A | N/A |
Indicate
by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange
Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2)
has been subject to such filing requirements for the past 90 days. Yes ☐
Indicate
by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data
File required to be submitted and posted pursuant to Rule 405 of Regulation S–T (§232.405 of this chapter) during the preceding
12 months (or for such shorter period that the registrant was required to submit and post such files). Yes ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non–accelerated filer, a smaller reporting company, or an emerging growth company.
| Large accelerated filer ☐ | Accelerated filer ☐ |
| Smaller
reporting company | |
| Emerging
Growth Company |
If an emerging growth company, indicate by check mark if the Registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards pursuant to Section 13(a) of the Exchange Act. ☐
Indicate
by check mark whether the registrant is a shell company (as defined in Rule 12b–2 of the Exchange Act). Yes ☐ No
As of August 19, 2026, there were shares of common stock and 12,000,000 shares of Series B preferred stock issued and outstanding.
TABLE OF CONTENTS
| 2 |
Nutra Pharma Corp (“Nutra Pharma”) and its wholly owned subsidiaries, Designer Diagnostics Inc. and ReceptoPharm, Inc. (“ReceptoPharm”), are referred to herein as “we”, “our” or “us” (Designer Diagnostics Inc. has been inactive since June 2011, ReceptoPharm is individually referred to herein).
Forward Looking Statements
This Quarterly Report on Form 10–Q for the period ending June 30, 2026, contains forward–looking statements that involve risks and uncertainties, as well as assumptions that if they never materialize or prove incorrect, could cause our results to differ materially from those expressed or implied by such forward–looking statements. The words or phrases “would be,” “will allow, “intends to,” “will likely result,” “are expected to,” “will continue,” “is anticipated,” “estimate,” “project,” or similar expressions are intended to identify “forward–looking statements.” We are subject to risks detailed in Item 1(a). All statements other than statements of historical fact are statements that could be deemed forward–looking statements, including: (a) any projections of revenue, gross margin, expenses, earnings or losses from operations, synergies or other financial items; and (b) any statements of the plans, strategies and objectives of management for future operations; and (c) any statement concerning developments, plans, or performance. Unless otherwise required by applicable law, we do not undertake and we specifically disclaim any obligation to update any forward–looking statements to reflect occurrences, developments, unanticipated events or circumstances after the date of such statement.
| 3 |
PART I. FINANCIAL INFORMATION
Item 1. Financial Statements
NUTRA PHARMA CORP.
Condensed Consolidated Balance Sheets
| June 30, | December 31, | |||||||
| 2026 | 2025 | |||||||
| (Unaudited) | ||||||||
| ASSETS | ||||||||
| Current assets: | ||||||||
| Cash | $ | $ | ||||||
| Accounts receivable | ||||||||
| Accounts receivable - related party, net | ||||||||
| Inventory, current portion | ||||||||
| Other receivable | ||||||||
| Convertible notes receivable, net of discount | ||||||||
| Receivable from sale of Stemsation stocks, net | ||||||||
| Investment in Stemsation stocks | ||||||||
| Settlement receivables | ||||||||
| Prepaid expenses and other current assets | ||||||||
| Total current assets | ||||||||
| Inventory, less current portion | ||||||||
| Due from employee - related party, net | ||||||||
| Property and equipment, net | ||||||||
| Total assets | $ | $ | ||||||
| LIABILITIES AND STOCKHOLDERS’ DEFICIT | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | $ | ||||||
| Accrued expenses | ||||||||
| Accrued payroll due to officers | ||||||||
| Accrued interest to related parties | ||||||||
| Due to related parties | ||||||||
| Derivative liabilities | ||||||||
| Notes payable – Unrelated third parties, net | ||||||||
| Convertible notes payable – Unrelated third parties, net | ||||||||
| Convertible notes payable, at fair value | ||||||||
| Other advances from an unrelated third party | ||||||||
| SBA notes payable, current portion | ||||||||
| Total current liabilities | ||||||||
| SBA notes payable, less current portion | ||||||||
| Total liabilities | ||||||||
| Commitments and Contingencies (Note 11) | ||||||||
| Stockholders’ deficit: | ||||||||
| Preferred stock, $ par value, shares authorized and Series B Preferred shares authorized, issued and outstanding | ||||||||
| Common stock, $ par value, shares authorized; and shares issued and outstanding, respectively | ||||||||
| Common stock to be issued | ||||||||
| Additional paid-in capital | ||||||||
| Accumulated deficit | ( | ) | ( | ) | ||||
| Total stockholders’ deficit | ( | ) | ( | ) | ||||
| Total liabilities and stockholders’ deficit | $ | $ | ||||||
See the accompanying notes to the unaudited condensed consolidated financial statements
| F-1 |
NUTRA PHARMA CORP.
Condensed Consolidated Statements of Operations
(Unaudited)
For the Three Months Ended June 30, | For the Six Months Ended June 30, | |||||||||||||||
| 2026 | 2025 | 2026 | 2025 | |||||||||||||
| Net sales | $ | $ | $ | $ | ||||||||||||
| Net sales to a related party | ||||||||||||||||
| Cost of sales | ( | ) | ( | ) | ( | ) | ( | ) | ||||||||
| Reserve for supplier advances for purchases | ( | ) | ||||||||||||||
| Gross profit | ||||||||||||||||
| Operating expenses: | ||||||||||||||||
| Payroll, benefits and related taxes | ||||||||||||||||
| Professional fees | ||||||||||||||||
| Consulting expenses | ||||||||||||||||
| Other selling, general and administrative costs | ||||||||||||||||
| Total operating expenses | ||||||||||||||||
| Loss from operations | ( | ) | ( | ) | ( | ) | ( | ) | ||||||||
| Other income (expenses) | ||||||||||||||||
| Other income | ||||||||||||||||
| Interest expense | ( | ) | ( | ) | ( | ) | ( | ) | ||||||||
| Interest expense to related parties | ( | ) | ( | ) | ( | ) | ( | ) | ||||||||
| Change in fair value of convertible notes and derivatives | ( | ) | ( | ) | ( | ) | ||||||||||
| Net gain on settlement of debt and accrued expenses | ||||||||||||||||
| Total other expenses, net | ( | ) | ( | ) | ( | ) | ||||||||||
| Loss before income taxes | ( | ) | ( | ) | ( | ) | ||||||||||
| Provision for income taxes | ||||||||||||||||
| Net (loss) income | $ | ( | ) | $ | $ | ( | ) | $ | ( | ) | ||||||
| Net loss per share - basic and diluted | $ | ) | $ | $ | ) | $ | ) | |||||||||
| Weighted average number of shares outstanding during the period - basic | ||||||||||||||||
| Weighted average number of shares outstanding during the period - diluted | ||||||||||||||||
See the accompanying notes to the unaudited condensed consolidated financial statements
| F-2 |
NUTRA PHARMA CORP.
Condensed Consolidated Statements of Changes in Stockholders’ Deficit
For the Three Months Ended June 30, 2026 and 2025
(Unaudited)
| Preferred Stock Series B | Common Stock | Common Stock to be issued | Additional Paid-in | Accumulated | Total Stockholders’ | |||||||||||||||||||||||||||||||
| Shares | Amount | Shares | Amount | Shares | Amount | Capital | Deficit | Deficit | ||||||||||||||||||||||||||||
| Balance -March 31, 2026 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
| Common stock to be issued for stock based compensation | - | - | ||||||||||||||||||||||||||||||||||
| Net loss | - | - | - | ( | ) | ( | ) | |||||||||||||||||||||||||||||
| Balance -June 30, 2026 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
| Preferred Stock Series B | Common Stock | Common Stock to be issued | Additional Paid-in | Accumulated | Total Stockholders’ | |||||||||||||||||||||||||||||||
| Shares | Amount | Shares | Amount | Shares | Amount | Capital | Deficit | Deficit | ||||||||||||||||||||||||||||
| Balance -March 31, 2025 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
| Common stock to be issued for stock based compensation | - | |||||||||||||||||||||||||||||||||||
| Net income | - | - | - | |||||||||||||||||||||||||||||||||
| Balance -June 30, 2025 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
See the accompanying notes to the unaudited condensed consolidated financial statements
| F-3 |
NUTRA PHARMA CORP.
Condensed Consolidated Statements of Changes in Stockholders’ Deficit
For the Six Months Ended June 30, 2026 and 2025
(Unaudited)
Preferred Stock Series B | Common Stock | Common Stock to be issued | Additional Paid-in | Accumulated | Total Stockholders’ | |||||||||||||||||||||||||||||||
| Shares | Amount | Shares | Amount | Shares | Amount | Capital | Deficit | Deficit | ||||||||||||||||||||||||||||
| Balance -December 31, 2025 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
| Common stock to be issued for stock based compensation | - | - | ||||||||||||||||||||||||||||||||||
| Common stock issued for settlement of debt | - | - | ( | ) | ||||||||||||||||||||||||||||||||
| Net loss | - | - | - | ( | ) | ( | ) | |||||||||||||||||||||||||||||
| Balance -June 30, 2026 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
Preferred Stock Series B | Common Stock | Common Stock to be issued | Additional Paid-in | Accumulated | Total Stockholders’ | |||||||||||||||||||||||||||||||
| Shares | Amount | Shares | Amount | Shares | Amount | Capital | Deficit | Deficit | ||||||||||||||||||||||||||||
| Balance -December 31, 2024 | $ | $ | $ | $ | ( | ) | $ | ( | ) | |||||||||||||||||||||||||||
| Common stock to be issued for stock based compensation | - | - | ||||||||||||||||||||||||||||||||||
| Net loss | - | - | - | ( | ) | ( | ) | |||||||||||||||||||||||||||||
| Balance -June 30, 2025 | $ | $ | $ | $ | $ | ( | ) | $ | ( | ) | ||||||||||||||||||||||||||
See the accompanying notes to the unaudited condensed consolidated financial statements
| F-4 |
NUTRA PHARMA CORP.
Condensed Consolidated Statements of Cash Flows
(Unaudited)
| For the Six Months Ended June 30, | ||||||||
| 2026 | 2025 | |||||||
| Cash flows from operating activities: | ||||||||
| Net loss | $ | ( | ) | $ | ( | ) | ||
| Adjustments to reconcile net loss to net cash used in operating activities: | ||||||||
| Change in reserve for supplier advances for purchases | ||||||||
| Net gain on settlement of debt and accrued expenses | ( | ) | ( | ) | ||||
| Depreciation | ||||||||
| Stock-based compensation | ||||||||
| Amortization of convertible notes receivable discount | ( | ) | ||||||
| Change in fair value of convertible notes and derivatives | ||||||||
| Amortization of loan discount | ||||||||
| Amortization of operating lease right-of-use assets | ||||||||
| Changes in operating assets and liabilities: | ||||||||
| Increase in accounts receivable | ( | ) | ( | ) | ||||
| Decrease (increase) in accounts receivable - related party, net | ( | ) | ||||||
| Decrease in inventory | ||||||||
| Increase in other receivable | ( | ) | ||||||
| Increase in due from employee - related party, net | ( | ) | ||||||
| Increase in prepaid expenses and other current assets | ( | ) | ( | ) | ||||
| (Decrease) increase in accounts payable | ( | ) | ||||||
| Increase in accrued expenses | ||||||||
| Increase in accrued payroll due to officers | ||||||||
| Increase in due to a related party | ||||||||
| Increase (decrease) in accrued interest to related parties | ||||||||
| Decrease in operating lease obligations | ( | ) | ||||||
| Net cash used in operating activities | ( | ) | ( | ) | ||||
| Cash flows from investing activities: | ||||||||
| Purchase of property and equipment | ( | ) | ||||||
| Convertible notes receivable advances | ( | ) | ||||||
| Net cash used in investing activities | ( | ) | ||||||
| Cash flows from financing activities: | ||||||||
| Advances from related parties | ||||||||
Repayments to related parties | ( | ) | ( | ) | ||||
| Proceeds from convertible notes | ||||||||
| Repayment of convertible notes | ( | ) | ( | ) | ||||
| Advances from notes payable | ||||||||
| Repayments of notes payable | ( | ) | ( | ) | ||||
| Net cash provided by financing activities | ||||||||
| Net change in cash | ( | ) | ||||||
| Cash - beginning of period | ||||||||
| Cash - end of period | $ | $ | ||||||
| Supplemental Cash Flow Information: | ||||||||
| Cash paid for interest | $ | $ | ||||||
| Cash paid for income taxes | $ | $ | ||||||
| Non Cash Financing and Investing: | ||||||||
| Common stock to be issued for stock based compensation | $ | $ | ||||||
| Common stock issued for settlement of debt | $ | $ | ||||||
See the accompanying notes to the unaudited condensed consolidated financial statements
| F-5 |
NUTRA PHARMA CORP.
Notes to Unaudited Condensed Consolidated Financial Statements
June 30, 2026
1. BASIS OF PRESENTATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Organization
Nutra Pharma Corp. (“Nutra Pharma”, the “Company,” “we,” “us,” or “our”), is a holding company that owns intellectual property and operates in the biotechnology industry. Nutra Pharma was incorporated under the laws of the state of California on February 1, 2000, under the original name of Exotic-Bird.com.
Through its wholly-owned subsidiary, ReceptoPharm, Inc. (“ReceptoPharm”), Nutra Pharma conducts drug discovery research and development activities. In October 2009, Nutra Pharma launched its first consumer product called Cobroxin®, an over-the-counter pain reliever designed to treat moderate to severe chronic pain. In May 2010, Nutra Pharma launched its second consumer product called Nyloxin®, an over-the-counter pain reliever that is a stronger version of Cobroxin® and is designed to treat severe chronic pain. In December 2014, Nutra Pharma launched Pet Pain-Away, an over-the-counter pain reliever designed to treat pain in cats and dogs. In October 2019, Nutra Pharma launched Equine Pain-Away™, an over-the-counter topical pain reliever designed to treat pain and inflammation in horses. In March 2021, Nutra Pharma launched Luxury Feet™, an over-the-counter pain reliever designed specifically to treat foot pain and inflammation especially for women that wear high heels and stilettos.
Basis of Presentation and Consolidation
The Unaudited Condensed Consolidated Financial Statements and notes are presented in accordance with accounting principles generally accepted in the United States of America (“U.S. GAAP”) and do not contain certain information included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025. In the opinion of management, all adjustments considered necessary for a fair presentation have been included and are of a normal, recurring nature. Interim results are not necessarily indicative of results for a full year. Therefore, the interim Unaudited Condensed Consolidated Financial Statements should be read in conjunction with the audited Consolidated Financial Statements and notes thereto contained in the Company’s Annual Report on Form 10-K from which the accompanying condensed consolidated balance sheet dated December 31, 2025 was derived.
The accompanying Unaudited Condensed Consolidated Financial Statements include the results of Nutra Pharma and its wholly-owned subsidiaries Designer Diagnostics Inc. and ReceptoPharm (collectively “the Company”, “us”, “we” or “our”). We operate as one reportable segment. Designer Diagnostics Inc. has been inactive since June 2011. All intercompany transactions and balances have been eliminated in consolidation. The results for the interim period presented are not necessarily indicative of the results that may be expected for the full fiscal year.
Reclassification of Prior Year Presentation
Reclassification occurred to certain prior period amounts in order to conform to the current period classifications. The reclassifications have no effect on the reported net loss.
Liquidity and Going Concern
Our
Unaudited Condensed Consolidated Financial Statements are presented on a going concern basis, which contemplate the realization of assets
and satisfaction of liabilities in the normal course of business. We have experienced recurring, significant losses from operations,
and have an accumulated deficit of $
There is substantial doubt regarding our ability to continue as a going concern which is contingent upon our ability to secure additional financing, increase ownership equity and attain profitable operations. In addition, our ability to continue as a going concern must be considered in light of the problems, expenses and complications frequently encountered in established markets and the competitive environment in which we operate.
We do not have sufficient cash to sustain our operations for a period of twelve months from the filing date of this quarterly report and will require additional financing in order to execute our operating plan and continue as a going concern. Since our sales are not currently adequate to fund our operations, we continue to rely principally on debt and equity funding; however, proceeds from such funding have not been sufficient to execute our business plan. The Company’s common stock is presently on the OTC Market Group’s Expert Market, which means that the Company’s common stock is not eligible for proprietary broker-dealer quotes. As this limits our ability to raise capital, our plan is to attempt to secure adequate funding through notes payable until sales of our pain products are adequate to fund our operations. We cannot predict whether additional financing will be available, and/or whether any such funding will be in the form of equity, debt, or another form. In the event that these financing sources do not materialize, or if we are unsuccessful in increasing our revenues and profits, we will be unable to implement our current plans for expansion, repay our obligations as they become due and continue as a going concern.
| F-6 |
The accompanying Unaudited Condensed Consolidated Financial Statements do not include any adjustments relating to the recoverability and classification of recorded asset amounts or the amounts and classification of liabilities that might be necessary should we be unable to continue as a going concern.
Use of Estimates
The accompanying Unaudited Condensed Consolidated Financial Statements are prepared in accordance with U.S. GAAP which require management to make estimates and assumptions. These estimates and assumptions affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenue and expense. Significant estimates include our ability to continue as a going concern, the recoverability of inventories and long-lived assets, the recoverability of receivables, the valuation of certain debt and derivative liabilities, recognition of loss contingencies and deferred tax valuation allowances. Actual results could differ from those estimates. Changes in facts and circumstances may result in revised estimates, which would be recorded in the period in which they become known.
Revenue from Contracts with Customers
The Company accounts for revenue from contracts with customers in accordance with Financial Accounting Standard Board (“FASB”) Accounting Standard Codification (“ASC”) Topic 606, Revenue from Contracts with Customers (“ASC 606”). Under ASC Topic 606, revenue recognition has a five-step process: a) Determine whether a contract exists; b) Identify the performance obligations; c) Determine the transaction price; d) Allocate the transaction price; and e) Recognize revenue when (or as) performance obligations are satisfied.
Our revenues are primarily derived from customer orders for the purchase of our products. We recognize revenues as performance obligations are fulfilled upon shipment of products. We record revenues net of promotions and discounts.
Accounting for Shipping and Handling Costs
We account for shipping and handling as fulfilment activities and record amounts billed to customers as revenue and the related shipping and handling costs as cost of sales.
Accounts Receivable and Allowance for Credit Loss
We grant credit without collateral to our customers based on our evaluation of a particular customer’s credit worthiness. Accounts receivable are due 30 days after the issuance of the invoice. The Company maintains an allowance for credit losses to reflect the current expected credit losses (“CECL”) over the contractual life of the receivables. Accounts receivable are written off after collection efforts have been deemed to be unsuccessful. Accounts written off as uncollectible are deducted from the allowance for credit losses, while subsequent recoveries are netted against the provision for doubtful accounts expense. We generally do not charge interest on accounts receivable. We use third party payment processors and are required to maintain reserve balances, which are included in accounts receivable.
Accounts
receivable are stated at estimated net realizable value. Accounts receivable are comprised of balances due from customers and a third
party payment processor, net of estimated allowances for uncollectible accounts.
At
June 30, 2026 and December 31, 2025, the Company recorded a provision for credit losses of $
| F-7 |
Inventories
Inventories, which are stated at the lower of average cost or net realizable value, consist of packaging materials, finished products, and raw venom that is utilized to make the API (active pharmaceutical ingredient). The raw unprocessed venom has an indefinite life for use. We classify inventory as short-term or long-term inventory based on timing of when it is expected to be consumed. The Company regularly reviews inventory quantities on hand. If necessary, it records a net realizable value adjustment for excess and obsolete inventory based primarily on its estimates of product demand and production requirements. Write-downs are charged to cost of sales. We performed an evaluation of our inventory and related accounts at June 30, 2026 and December 31, 2025, and determined no reserves were necessary.
Financial Instruments
Our financial instruments include cash, accounts receivable, accounts payable, accrued expenses, loans payable, due to officers and derivative financial instruments. Other than certain convertible instruments (derivative financial instruments) and liabilities to related parties (for which it was impracticable to estimate fair value due to uncertainty as to when they will be satisfied and a lack of similar type transactions in the marketplace), we believe the carrying values of our financial instruments approximate their fair values because they are short term in nature or payable on demand. Our derivative financial instruments are carried at a measured fair value.
Cash and cash equivalents
The
Company maintains cash balances in a non-interest-bearing account that currently does not exceed federally insured limits of $
Concentration of Credit Risk
Balances
in various cash accounts may at times exceed federally insured limits. We have not experienced any losses in such accounts. We do not
hold or issue financial instruments for trading purposes. For the three and six months ended June 30, 2026, sales to Avini Health (“Avini”),
a related party, accounted for approximately
| F-8 |
Derivative Financial Instruments
Management evaluates all of its financial instruments to determine if such instruments are derivatives or contain features that qualify as embedded derivatives. For derivative financial instruments that are accounted for as liabilities, the derivative instrument is initially recorded at its fair value and is then re-valued at each reporting date, with changes in the fair value reported as charges or credits to other income. The classification of derivative instruments, including whether such instruments should be recorded as liabilities or as equity, is re-assessed at the end of each reporting period. Derivative instrument liabilities are classified in the balance sheet as current or non-current based on whether or not net-cash settlement of the derivative instrument could be required within 12 months of the balance sheet date.
We do not use derivative instruments to hedge exposures to cash flow, market, or foreign currency risks.
Convertible Debt
The Company adheres to ASU 2020-06, Debt—Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging—Contracts in Entity’s Own Equity (Subtopic 815-40). This ASU eliminates certain separation models, including the beneficial conversion feature and cash conversion models, so convertible instruments issued after adoption are generally accounted for as a single liability or equity instrument, unless a conversion feature requires separate derivative accounting under ASC 815. ASU 2020-06 also amends diluted EPS guidance.
The Fair Value Measurement Option
We have elected the fair value measurement option for convertible debt with embedded derivatives that require bifurcation, and record the entire hybrid financing instrument at fair value under the guidance of ASC Topic 815, Derivatives and Hedging (“ASC Topic 815”). The Company reports interest expense, including accrued interest, related to this convertible debt under the fair value option, within the change in fair value of convertible notes and derivatives in the accompanying condensed consolidated statements of operations.
Derivative Accounting for Convertible Debt
The Company evaluated the terms and conditions of the convertible debt under the guidance of ASC Topic 815, Derivatives and Hedging. The conversion terms of some of the convertible notes are variable based on certain factors, such as the future price of the Company’s common stock. The number of shares of common stock to be issued is based on the future price of the Company’s common stock. The number of shares of common stock issuable upon conversion of the debt is indeterminate. Due to the fact that the number of shares of common stock issuable could exceed the Company’s authorized share limit, the equity environment is tainted, and all additional convertible debt are included in the value of the derivative liabilities. Pursuant to ASC 815-15, Embedded Derivatives, the fair values of the convertible debt and shares to be issued were recorded as derivative liabilities on the issuance date and revalued at each reporting period.
Debt Modifications and Extinguishments
The Company evaluates amendments, restatements, or other changes to its debt agreements in accordance with ASC 470-50, Debt — Modifications and Extinguishments. Under this guidance, we determine whether the revised terms represent a modification of the existing debt or an extinguishment of the old debt and issuance of new debt. If the changes are not deemed substantial, the transaction is accounted for as a modification and any associated fees or costs are amortized over the remaining term of the modified debt. If the changes are determined to be substantial, the original debt is considered extinguished, the new debt is recorded at fair value, and any resulting difference between the carrying amount of the old debt and the fair value of the new debt is recognized in earnings as a gain or loss on extinguishment.
| F-9 |
Property and Equipment
Property
and equipment is recorded at cost. Expenditures for major improvements and additions are added to property and equipment, while replacements,
maintenance and repairs which do not extend the useful lives are expensed. Depreciation is computed using the straight-line method over
the estimated useful lives of the assets of
Long-Lived Assets
The carrying value of long-lived assets is reviewed annually and on a regular basis for the existence of facts and circumstances that may suggest impairment. If indicators of impairment are present, we determine whether the sum of the estimated undiscounted future cash flows attributable to the long-lived asset in question is less than its carrying amount. If less, we measure the amount of the impairment based on the amount that the carrying value of the impaired asset exceeds the discounted cash flows expected to result from the use and eventual disposal of the impaired assets.
Income Taxes
The Company recorded no income tax expense for the six months ended June 30, 2026 and 2025 because the estimated annual effective tax rate was zero. The Company applies the asset and liability method of accounting for income taxes, under which deferred tax assets and liabilities are recognized for temporary differences between the financial reporting basis and the tax basis of the Company’s assets and liabilities, as well as for net operating loss and tax credit carryforwards. Deferred tax assets are reduced by a valuation allowance when, based on available evidence, it is more likely than not that some portion or all of the deferred tax assets will not be realized.
As of June 30, 2026 and December 31, 2025, the Company continues to maintain a full valuation allowance against its net deferred tax assets due to a history of operating losses and the uncertainty regarding the Company’s ability to generate sufficient future taxable income to realize such assets. The Company’s federal and state income tax returns for 2021 to 2025 remain open for examination by taxing authorities.
We account for stock-based compensation in accordance with FASB ASC Topic 718, Stock Compensation (“ASC Topic 718”) which requires that the cost resulting from all share-based transactions be recorded in the financial statements over the respective service periods. It establishes fair value as the measurement objective in accounting for share-based payment arrangements and requires all entities to apply a fair-value-based measurement in accounting for share-based payment transactions with employees. The statement also establishes fair value as the measurement objective for transactions in which an entity acquires goods or services from non-employees in share-based payment transactions.
Net income (loss) per share is calculated in accordance with FASB ASC Topic 260, Earnings per Share. Basic income (loss) per share is calculated by dividing net income (loss) by the weighted average number of common shares outstanding for the period. Diluted income (loss) per share is calculated by dividing net income (loss) by the weighted average number of common shares and dilutive common stock equivalents outstanding. During periods in which we incur losses, common stock equivalents, if any, are not considered, as their effect would be anti-dilutive or have no effect on earnings per share. Any common shares issued as of a result of the exercise of conversion options would come from newly issued common shares from our remaining authorized shares.
| Three Months Ended | ||||||||
| June 30, | ||||||||
| 2026 | 2025 | |||||||
| Basic and diluted numerator: | ||||||||
| Net income (loss) - basic | $ | ( | ) | $ | ||||
| Effect of dilutive securities: | ||||||||
| Change in fair value of convertible notes | ||||||||
| Interest on convertible debt | ||||||||
| Net income (loss) - diluted | $ | ( | ) | $ | ||||
| Basic and diluted denominator: | ||||||||
| Weighted-average common shares outstanding - basic | ||||||||
| Effect of dilutive securities: | ||||||||
| Convertible debt | ||||||||
| Weighted-average common shares outstanding - diluted (1) | ||||||||
| Net income (loss) per share - basic and diluted | $ | ) | $ | |||||
| (1) |
| F-10 |
| June 30, 2026 | June 30, 2025 | |||||||
| Convertible notes payable at fair value | ||||||||
| Convertible notes payable | ||||||||
| Total | ||||||||
The following table summarizes the weighted average securities that were excluded from the diluted per share calculation because for the six months ended June 30, 2026 and 2025, the effect of including these potential shares was antidilutive due to a net loss:
| June 30, 2026 | June 30, 2025 | |||||||
| Convertible notes payable at fair value | ||||||||
| Convertible notes payable | ||||||||
| Total | ||||||||
Segment Reporting
The Company adheres to ASU No. 2023-07, Codification Improvements to Segment Reporting (Topic 280) (“ASU 2023-07”), which provides clarifications and improvements to the existing segment reporting requirements, including updates related to the aggregation criteria, reconciliation of segment measures to unaudited condensed consolidated financial statements, and disclosure requirements.
The Company operates as a single reportable operating segment. Operating segments are identified based on the manner in which the Company’s Chief Operating Decision Maker (“CODM”), who is the Company’s Chief Executive Officer, reviews financial information for purposes of allocating resources and assessing performance.
The CODM reviews financial results and manages the business on a consolidated basis, without differentiation by product line, geographic region, or legal entity. Accordingly, the Company has determined that it has one operating and one reportable segment.
Recent Accounting Pronouncements
Adopted Pronouncements
Effective January 1, 2026, the Company adopted ASU No. 2024-04, Debt—Debt with Conversion and Other Options (Subtopic 470-20): Accounting for Convertible Debt Instruments (“ASU 2024-04”), which amends existing guidance to clarify and refine the recognition, measurement, presentation, and disclosure requirements for certain convertible debt arrangements, including matters related to classification, embedded features, and related disclosures. The amendments are intended to improve consistency and comparability in the accounting for convertible debt instruments. The adoption of this ASU did not have a material effect on the accompanying unaudited condensed consolidated financial statements.
Effective January 1, 2026, the Company adopted ASU No. 2025-05, Financial Instruments—Credit Losses (Topic 326): Improvements to Credit Loss Guidance (“ASU 2025-05”), which amends the existing guidance under the current expected credit losses (“CECL”) model to clarify and refine the requirements related to the measurement, presentation, and disclosure of credit losses for financial assets measured at amortized cost. The adoption of this ASU did not have a material effect on the accompanying unaudited condensed consolidated financial statements.
Not Yet Effective Pronouncements
The Company has evaluated the impact of the recently issued accounting standards that had not been adopted as of June 30, 2026:
ASU No. 2024-03, Income Statement—Reporting Comprehensive Income—Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses (“ASU 2024-03”), requires public business entities to provide additional disaggregated disclosures related to certain expense captions presented on the face of the income statement. The amendments are intended to improve the transparency and usefulness of expense information provided to financial statement users. This guidance is effective for the Company for annual reporting periods beginning after December 15, 2026, and interim reporting periods beginning after December 15, 2027. The Company is currently evaluating the impact of adopting this standard on its unaudited condensed consolidated financial statements.
ASU No. 2025-04, Compensation—Stock Compensation (Topic 718) and Revenue from Contracts with Customers (Topic 606): Clarifications to Share-Based Consideration Payable to a Customer (“ASU 2025-04”), clarifies the accounting guidance related to share-based consideration payable to customers, including matters related to performance conditions, forfeitures, and the application of the variable consideration guidance. The amendments are intended to improve consistency in the accounting for share-based consideration arrangements with customers. This guidance is effective for the Company beginning January 1, 2027. The Company is currently evaluating the impact of adopting this standard on its unaudited condensed consolidated financial statements.
ASU No. 2025-12, Codification Improvements (“ASU 2025-12”), includes amendments to the FASB Accounting Standards Codification intended to correct, clarify, and improve various aspects of existing accounting guidance. The amendments address a broad range of topics, including earnings per share, lease receivables, treasury stock retirements, and transfers of receivables from contracts with customers. This guidance is effective for the Company for annual reporting periods beginning after December 15, 2026, and interim reporting periods within those annual reporting periods. The Company is currently evaluating the impact of adopting this standard on its unaudited condensed consolidated financial statements.
The Company determined that any other standards not yet effective are either not applicable or are not expected to have a material impact on the Company’s unaudited condensed consolidated financial statements.
2. FAIR VALUE MEASUREMENTS
Certain assets and liabilities that are measured at fair value on a recurring basis at June 30, 2026 and December 31, 2025 are measured in accordance with FASB ASC Topic 820-10-05, Fair Value Measurements. FASB ASC Topic 820-10-05 defines fair value, establishes a framework for measuring fair value and expands the disclosure requirements regarding fair value measurements for financial assets and liabilities as well as for non-financial assets and liabilities that are recognized or disclosed at fair value on a recurring basis in the unaudited condensed consolidated financial statements.
The statement requires fair value measurement be classified and disclosed in one of the following three categories:
| Level 1: | Unadjusted quoted prices in active markets that are accessible at the measurement date for identical unrestricted assets or liabilities; | |
| Level 2: | Quoted prices in markets that are not active or inputs which are observable either directly or indirectly for substantially the full term of the asset or liability; and | |
| Level 3: | Prices or valuation techniques that require inputs that are both significant to the fair value measurement and unobservable (i.e. supported by little or no market activity). |
| F-11 |
The following table summarizes our financial instruments measured at fair value at June 30, 2026 and December 31, 2025:
| Fair Value Measurements at June 30, 2026 | ||||||||||||||||
| Total | Level 1 | Level 2 | Level 3 | |||||||||||||
| Liabilities: | ||||||||||||||||
| Derivative liabilities | $ | $ | $ | $ | ||||||||||||
| Convertible notes at fair value | $ | $ | $ | $ | ||||||||||||
| Fair Value Measurements at December 31, 2025 | ||||||||||||||||
| Total | Level 1 | Level 2 | Level 3 | |||||||||||||
| Liabilities: | ||||||||||||||||
| Derivative liabilities | $ | $ | $ | $ | ||||||||||||
| Convertible notes at fair value | $ | $ | $ | $ | ||||||||||||
We valued derivative liabilities using the number of potential convertible shares for convertible notes with fixed conversion price that are recorded at amortized cost times the closing stock price of our restricted common stock at June 30, 2026 and December 31, 2025. These derivative liabilities are recorded due to the fact that the number of shares of common stock issuable could exceed the Company’s authorized share limit and the equity environment is tainted, and therefore all convertible debt should be accounted for as liabilities.
The following table summarizes assumptions and the significant terms of the convertible notes for which the entire hybrid instrument is recorded at fair value at June 30, 2026 and December 31, 2025:
Conversion Price - Lower of Fixed Price or Percentage of VWAP for Look-back Period | ||||||||||||||||||||||||
| Debenture | Face Amount | Interest Rate | Default Interest Rate | Discount Rate | Anti-Dilution Adjusted Price | % of stock price for look-back period | Look-back Period | |||||||||||||||||
| June 30, 2026 | $ | N/A | $ | |||||||||||||||||||||
| December 31, 2025 | $ | N/A | $ | |||||||||||||||||||||
| F-12 |
Using the stated assumptions summarized in the table above, we calculated the inception date and reporting period fair values of each note issued. The following table shows the changes in fair value measurements for the convertible notes at fair value using significant unobservable inputs (Level 3) during the six months ended June 30, 2026 and the year ended December 31, 2025:
| Description | June 30, 2026 | December 31, 2025 | ||||||
| Beginning balance | $ | $ | ||||||
| Loss from change in fair value (1) | ||||||||
| Ending balance | $ | $ | ||||||
| (1) |
3. INVENTORIES
Inventories are valued at the lower of cost or net realizable value on an average cost basis. At June 30, 2026 and December 31, 2025, inventories were as follows:
June 30, 2026 | December 31, 2025 | |||||||
| Raw Materials | $ | $ | ||||||
| Finished Goods | ||||||||
| Total Inventories | ||||||||
| Less: Long-term inventory | ( | ) | ( | ) | ||||
| Current portion | $ | $ | ||||||
4. PROPERTY AND EQUIPMENT
Property and equipment consists of the following at June 30, 2026 and December 31, 2025:
June 30, 2026 | December 31, 2025 | |||||||
| Furniture and fixtures | $ | $ | ||||||
| Lab equipment | ||||||||
| Total | ||||||||
| Less: Accumulated depreciation | ( | ) | ( | ) | ||||
| Property and equipment, net | $ | $ | ||||||
We
review our long-lived assets for recoverability if events or changes in circumstances indicate the assets may be impaired. At June 30,
2026, we believe the carrying values of our long-lived assets are recoverable. Depreciation expense for the three-months ended June 30,
2026 and 2025 was $
| F-13 |
5. DUE TO RELATED PARTIES
At
June 30, 2026 and December 31, 2025, the balance due to an entity controlled by Rik Deitsch, the Company’s former CEO, was $
Due
to related parties also includes $
These transactions were not conducted on an arm’s-length basis and, as such, may differ from the terms that would have been negotiated with an unrelated third party.
6. DEBTS
Debts consist of the following at June 30, 2026 and December 31, 2025:
June 30, 2026 | December 31, 2025 | |||||||
| Notes payable – Unrelated third parties (Net of discount of $ and $, respectively) (1) | $ | $ | ||||||
| Convertible notes payable – Unrelated third parties (Net of discount of $ and $, respectively) (2) | ||||||||
| Convertible notes payable, at fair value (3) | ||||||||
| Other advances from an unrelated third party (4) | ||||||||
| SBA notes payable (5) | ||||||||
| Ending balances | ||||||||
| Less: Long-term portion- SBA notes payable | ( | ) | ( | ) | ||||
| Current portion | $ | $ | ||||||
| (1) |
| ● | In
August 2016, we issued two Promissory Notes for a total of $
The
Company made repayments totaling $ |
| F-14 |
| ● | On
August 2, 2011 under a settlement agreement with Liquid Packaging Resources, Inc. (“LPR”), we agreed to pay LPR a total
of $ | |
| ● | At
December 31, 2012, we owed University Centre West Ltd. approximately $ | |
| ● | In
April 2016, we issued a promissory note to an unrelated third party in the amount of $ | |
| ● | In
May 2016, the Company issued a promissory note to an unrelated third party in the amount of $ | |
| ● | In
June 2016, the Company issued a promissory note to an unrelated third party in the amount of $ | |
| ● | A
promissory note originally issued to an unrelated third party in August 2016 was restated in September 2019 in the amount of $ | |
| ● | On
September 26, 2016, we issued a promissory note to an unrelated third party in the amount of $ |
| F-15 |
| ● | In
October 2016, we issued a promissory note to an unrelated third party in the amount of $ | |
| ● | In
June 2017, we issued a promissory note to an unrelated third party in the amount of $ | |
| ● | During
July 2017, we received a loan for a total of $ | |
| ● | In
July 2017, we issued a promissory note to an unrelated third party in the amount of $ | |
| ● | In
November 2017, we issued a promissory note to an unrelated third party in the amount of $ | |
| ● | In
November 2017, we issued a promissory note to an unrelated third party in the amount of $ |
| F-16 |
| ● | In September 2025, the Company entered into a Purchase and Sale of Future Receipts Agreement with a third party. Pursuant to this agreement, the buyer purchased $ of the Company’s future receivables in exchange for total proceeds of $, on a non-recourse basis. The Company authorized the buyer to debit its bank account at a specified remittance frequency until the full purchased amount of $ was collected. In connection with this transaction, the Company recorded a total debt discount of $ related to loan origination fees and issuance costs, which is being amortized over the term of the agreement. Repayments of $ and $ were made during 2025 and the first two quarters of 2026, respectively. Amortization for the three months ended June 30, 2026 and 2025, was $ and $, respectively. Amortization for the six months ended June 30, 2026 and 2025, was $ and $, respectively. At June 30, 2026 and December 31, 2025, the principal balance, net of debt discount of $ and $, was $ and $, respectively. | |
| ● | In March 2026, the Company entered into a Purchase and Sale of Future Receipts Agreement with a third party. Pursuant to this agreement, the buyer purchased $ of the Company’s future receivables in exchange for total proceeds of $, on a non-recourse basis. The Company authorized the buyer to debit its bank account at a specified remittance frequency until the full purchased amount of $ was collected. In connection with this transaction, the Company recorded a total debt discount of $ related to loan origination fees and issuance costs, which is being amortized over the term of the agreement. Repayments of $ were made during the first two quarters of 2026. Amortization for the three and six months ended June 30, 2026 was $ and $, respectively. At June 30, 2026, the principal balance, net of debt discount of $, was $. |
| (2) |
| ● | In
October 2017, we issued a promissory note to an unrelated third party in the amount of $ | |
| ● | During
January through December 2018, we issued convertible notes payable to 14 unrelated third parties for a total of $ | |
| ● | During
February 2019, the Company issued convertible notes payable totaling $ |
| ● | During
November 2019, we issued a convertible promissory note to an unrelated third party for $ | |
| At
June 30, 2026 and December 31, 2025, the outstanding principal balance of the notes issued in 2019 was $ | ||
| ● | During
the year ended December 31, 2020, the Company issued convertible notes payable totaling $ |
| F-17 |
| ● | During
August 2021, a promissory note of $
In
February 2024, the principal balance and the related penalty for a total of $
In
February 2025, the note was further restated to extend its maturity date to February 2026, with the principal balance of $
In
February 2026, the note was further restated to extend its maturity date to February 2027, with the principal balance of $
The
Company evaluated the amendment to the note under applicable debt extinguishment guidance and concluded that the amended terms were
substantially different from the original terms, as the present value of the revised cash flows exceeded the
Amortization
of debt discount for the three and six months ended June 30, 2026 was $ | |
| ● | During
2021, we issued convertible promissory notes to unrelated third parties totaling $ | |
| ● | During
2022, we issued convertible promissory notes to unrelated third parties totaling $ | |
| ● | During
2022, convertible promissory notes totaling $ |
| ● | During
2023, the Company amended convertible promissory notes totaling $ | |
| ● | During
2023, the Company issued convertible promissory notes to unrelated third parties with a fixed conversion price of $ |
| F-18 |
| ● | During
2024, a convertible promissory note of $ | |
| ● | During
2024, the Company issued convertible promissory notes to unrelated third parties with fixed conversion prices ranging from $ | |
| ● | During
the second quarter of 2024, the Company settled convertible promissory notes with an aggregate principal balance of $ | |
| ● | During
the third quarter of 2024, the Company settled convertible promissory notes of $ | |
| ● | During 2025 through June 2026, we issued convertible promissory notes to unrelated third parties for a total of $ with aggregate original issuance discount of $. The noteholders have the right to convert the notes into shares of Common Stock at fixed conversion prices ranging from $ to $ per share. The notes are due one year from the execution and funding of the notes. In connection with the issuance of $ of these notes, we paid approximately 10% of the related proceeds to third parties, which has been recorded as additional debt discount. Both the original issue discount and the issuance-related costs are being amortized over the term of each tranche. $ of the above-mentioned notes are in default and under negotiation for settlement as of the date of this report. | |
| ● | During
July 2025, the Company settled a convertible promissory note with a principal balance of $ |
| F-19 |
| ● | In
January 2026, the Company entered into a settlement agreement with the holder of certain promissory notes originally issued in 2021
and 2022, pursuant to which the outstanding notes of $ | |
| ● | During
April 2026, the Company settled a convertible promissory note with a principal balance of $ | |
| ● | The
total discount amortization on all of the above mentioned convertible notes payable for the three months ended June 30, 2026 and
2025 was $ | |
| ● | At
June 30, 2026, $ |
| (3) |
| ● | The
balance of $ | |
| ● | During
May 2017, we issued a Convertible Debenture in the amount of $ | |
| ● | During
October 2020, we issued a Convertible Debenture in the amount of $ | |
| ● | During
July 2018, we issued a convertible debenture in the amount of $ |
| F-20 |
| ● | During
January 2019, we issued a convertible debenture in the amount of $ | |
| ● | During
June 2019, we issued a convertible promissory note to an unrelated third party for $ |
| (4) | |
| (5) |
At June 30, 2026, the future minimum principal payments for all debts are as follows:
| June 30, | Amount | |||
| 2027 | $ | |||
| 2028 | ||||
| 2029 | ||||
| 2030 | ||||
| 2031 | ||||
| Thereafter | ||||
| $ | ||||
| Less: Long-term portion SBA notes payable | ( | ) | ||
| Current portion | $ | |||
| F-21 |
7. STOCKHOLDERS’ DEFICIT
Series B Preferred Stock
Effective March 2021, pursuant to authority of its Board of Directors, the Company filed a Certificate of Determination for its Series B Preferred Stock. The Series B Preferred Stock has a par value of $ per shares and consists of shares.
Terms of the Series B Preferred include the following:
| 1. | The Series B Preferred votes with the Company’s common stock as a single class on all matters or consents for the Company’s common stockholders. Each share of Series B Preferred is entitled to one thousand votes per share. | |
| 2. | The Series B Preferred will not be entitled to dividends unless the Company pays cash dividends or dividends in other property to holders of outstanding shares of common stock, in which event, each outstanding share of the Series B Preferred will be entitled to receive dividends of cash or property in an amount or value equal to one thousand multiplied by the amount paid in respect of one share of common stock. Any dividend payable to the Series B Preferred will have the same record and payment date and terms as the dividend payable on the common stock. | |
| 3. | Upon any voluntary or involuntary liquidation, dissolution or winding up of the Company, the holders of all shares of Series B Preferred then outstanding shall be entitled to be paid out of the assets of the Company available for distribution to its stockholders an amount in cash equal to $ in cash per share before any distribution is made on any shares of the Company’s common stock. If upon any voluntary or involuntary liquidation, dissolution or winding up of the Company, the application of all amounts available for payments with respect to Series B Preferred would not result in payment in full of Series B Preferred, the holders shall share equally and ratably in any distribution of assets of the Company in proportion to the full liquidation preference to which each is entitled. | |
| 4. | The Series B Preferred does not have any redemption rights. |
Common Stock Issued for Services
On
May 1, 2025, the Company entered into a consulting agreement for services. Pursuant to the agreement, the Company agreed to issue up
to shares of restricted common stock as compensation over an initial 12-month service period, including an initial issuance
of shares upon execution and monthly issuances of shares beginning July 1, 2025. The initial shares
were issued in May 2025 and were valued at $
On
January 1, 2026, the Company entered into a consulting agreement for services. Pursuant to the agreement, the Company issued
shares of restricted common stock as compensation for a 12-month service period. The shares were valued at $
As of the date of this report, the above mentioned shares have not been issued by the transfer agent; however, the Company has recorded the shares as common stock to be issued and recognized the related stock based compensation expense.
Debt Settlement and Stock Issuance
In
January 2026, the Company entered into a settlement agreement with the holder of certain promissory notes originally issued in 2021 and
2022. As of the settlement date, the aggregate carrying value of the outstanding debt was approximately $
8. ACCRUED EXPENSES
Accrued expenses consist of the following:
June 30, 2026 | December 31, 2025 | |||||||
| Accrued consulting fees | $ | $ | ||||||
| Accrued settlement expenses (1) | ||||||||
| Accrued payroll taxes | ||||||||
| Accrued interest | ||||||||
| Accrued others | ||||||||
| Total | $ | $ | ||||||
| (1) |
| F-22 |
9. PREPAID EXPENSES
Prepaid expenses and other current assets consist of the following:
June 30, 2026 | December 31, 2025 | |||||||
| Supplier advances for venom | $ | $ | ||||||
| Reserve for supplier advances | ( | ) | ||||||
| Net supplier advances | ||||||||
| Prepaid stock based compensation (see Note 7) | ||||||||
| Prepaid professional fees | ||||||||
| Total | $ | $ | ||||||
We
performed an evaluation of our supplier advances for venom at December 31, 2025, and determined full reserves were
necessary. During the six months ended June 30, 2026, the Company wrote off $
10. CONVERTIBLE NOTES RECEIVABLE
During
2021 through 2023, we purchased an aggregate of $
On
June 5, 2023, the Company entered into a settlement agreement with StemSation to convert the notes receivable balances of $
Pursuant
to the agreement, the Company is entitled to receive shares of StemSation’s common stock in exchange for the full settlement
of the outstanding notes receivable. As of June 30, 2023, the Company recognized the settlement receivable at $
Between
July and November 2023, $
| Date of Conversion Notice | Conversion Amount | Number of Shares Issued | Value of Shares Issued ($/per share) at Issuance | |||||||||
| $ | ||||||||||||
| $ | ||||||||||||
| $ | ||||||||||||
Of
the shares issued, shares were sold in the third quarter of 2023 for total proceeds of $
In
March 2024, the Company sold an additional shares for $, the proceeds of which remained outstanding as of December 31,
2025. As a result, the gross receivable balance related to these transactions was $ at June 30, 2026 and December 31, 2025. As
of June 30, 2026 and December 31, 2025, the Company recorded a full allowance for credit losses against the outstanding receivable balance
based on management’s evaluation of collectability and current expected credit loss factors. The remaining shares converted
in November 2023, valued at $
During
May 2025, we purchased a convertible note for $
Convertible
notes receivable were $
| F-23 |
11. COMMITMENTS AND CONTINGENCIES
Consulting Agreements
During
July 2015, we signed an agreement with a company to provide consulting services for
During
October 2015, the Company signed an agreement with a consultant for consulting services for a year. In connection with the agreement,
shares of the Company’s restricted common stock were granted and the Company was to make monthly cash payments of $
During
September 2022, the Company renewed its consulting agreement with an external consultant for a three-year term, providing for monthly
compensation of $
On
January 1, 2025, the Company entered into an Agent and Representation Agreement with an external consulting company pursuant to which
the agent will solicit prospective commercial and contract manufacturing clients on behalf of the Company. Under the agreement, the Company
is obligated to pay referral commissions to the agent for clients introduced by the agent who purchase the Company’s products or
services. The agreement required an initial payment of $
On
May 1, 2025, the Company entered into a consulting agreement for services. Pursuant to the agreement, the Company agreed to issue up
to shares of restricted common stock as compensation over an initial 12-month service period, including an initial issuance
of shares upon execution and monthly issuances of shares beginning July 1, 2025. The initial shares
were issued in May 2025 and were valued at $
In
December 2025, the Company entered into a business collaboration agreement with a third-party service provider to support its
expansion into the Indian market. Under the agreement, the service provider will assist with business development activities,
including identifying potential customers, facilitating negotiations, and supporting market entry efforts. Under the agreement, the
Company paid a mobilization fee of $
On
January 1, 2026, the Company entered into a one-year consulting agreement with an external consultant, providing for monthly compensation
of $
| F-24 |
Litigation
CSA 8411, LLC v. Nutra Pharma Corp., Case No. CACE 18-023150
On
October 12, 2018, CSA 8411, LLC filed a lawsuit against the Company in the 17th Judicial Circuit Court in and for Broward County, Florida
(Case No. CACE 18-023150) to recover $
As
of June 30, 2026 and December 31, 2025, the Company had an outstanding principal balance of $
Securities and Exchange Commission v. Nutra Pharma Corporation, Erik Deitsch, and Sean Peter McManus
On September 28, 2018, the United States Securities and Exchange Commission (the “SEC”) filed a lawsuit in the United States District Court for the Eastern District of New York (Case No. 2:18-cv-05459) against the Company, Mr. Deitsch, and Mr. McManus. The lawsuit alleges that, from July 2013 through June 2018, the Company and the other defendants’ defrauded investors by making materially false and misleading statements about the Company and violated anti-fraud and other securities laws.
On May 29, 2019 (following each of the defendants filing motions to dismiss), the SEC filed a First Amended Complaint which generally alleged the same conduct as its original Complaint, but accounted for certain guidance provided by the United States Supreme Court in a case that had been recently decided. Each of the defendants then moved to dismiss the SEC’s First Amended Complaint. On June 30, 2020, the Court entered an Order granting in part and denying in part the various motions to dismiss. Following that Order, the SEC filed a Second Amended Complaint (the operative pleading) and the defendants have filed their answers which generally deny liability. At this time, discovery is closed and the SEC has indicated an intent to file a summary judgment motion regarding certain non-fraud claims asserted in its Second Amended Complaint. The defendants have opposed the SEC’s request to file such motion(s). The Court conducted a hearing on February 23, 2021 and set an initial briefing schedule for the SEC’s Motion for Partial Summary Judgment wherein the Plaintiffs’ Motion for Partial Summary Judgment was due on April 5, 2021, the Defendants’ Consolidated (i.e., collectively, Nutra Pharma Corporation, Erik “Rik” Deitsch, and Sean McManus) Response Brief to the SEC’s Motion was due May 3, 2021, and the Plaintiffs’ Reply Brief was due on May 19, 2021. On March 23, 2021, the Plaintiff filed a Motion for Extension of Time to file the Motion for Partial Summary Judgment. On April 9, 2021, the Plaintiff filed a Motion for Partial Summary Judgment, Defendants’ filed a Memorandum of Law in Opposition to Plaintiff’s Motion on May 7, 2021, and Plaintiff filed its Reply brief on May 21, 2021.
In
July 2024, a final judgment was issued, ordering the defendant to pay $
| F-25 |
Settlement with Marc Weller
In
January 2026, the Company entered into a settlement agreement with Marc Weller in connection with a dispute arising in the ordinary course
of business (See Note 6 and Note 7). As part of the settlement, the outstanding notes, with an aggregate carrying value of approximately
$
12. SEGMENT AND ENTITY-WIDE INFORMATION
The Company operates as a single reportable operating segment. Operating segments are identified based on the manner in which the Company’s Chief Operating Decision Maker (“CODM”), who is the Company’s Chief Executive Officer, reviews financial information for purposes of allocating resources and assessing performance.
The CODM reviews financial results and manages the business on a consolidated basis, without differentiation by product line, geographic region, or legal entity. Accordingly, the Company has determined that it has one operating and one reportable segment.
The measure of segment profit or loss used by the CODM is consolidated net loss, as reported in the condensed consolidated statements of operations. The significant expense categories included in the measure of segment profit or loss and regularly reviewed by the CODM include cost of goods sold, payroll, benefits and related taxes, professional fees, consulting expenses, other selling, general and administrative expenses.
The accounting policies of the reportable segment are the same as those described in the summary of significant accounting policies. The Company has no intersegment revenues.
For
the three and six months ended June 30, 2026, one third-party customer accounted for approximately
For
the three and six months ended June 30, 2026, sales to a related party, accounted for approximately
13. RELATED PARTY TRANSACTIONS
The Company acts as a product formulator and contract manufacturer for Avini Health (“Avini”). The Company’s former chief executive officer, who held that position through March 2024, is an owner of Avini and is its chief scientific officer. Following March 2024, this individual assumed the role of Operations Manager of the Company.
During September 2023, the sales and manufacturing structure between the Company and Avini was revised. Avini assumed responsibility for manufacturing its own products, and the Company transferred to Avini certain raw materials and packaging supplies related to amounts previously advanced by Avini. In connection with this transition, the Company relocated its operations to a Boca Raton facility leased by Avini. Under this arrangement, the Company uses the facility rent-free, shares space and resources with Avini, and Avini pays all lease and office-related expenses. Sales to Avini declined beginning in 2024 as Avini began to manufacture its own products; however, the Company benefits from reduced operating costs and continued access to manufacturing capabilities for its own Nutra Pharma–branded products.
As
of June 30, 2026 and December 31, 2025, the Company recorded accounts receivable from related party of $
| F-26 |
The Company had fully reserved receivables from
another company owned by the former CEO. The reserve was $
During
2010 we borrowed $
As of June 30, 2026 and December 31, 2025, we had the following related party balances:
| June 30, | December 31, | |||||||
| 2026 | 2025 | |||||||
| Account receivable – related party, net | $ | $ | ||||||
| Due from employee – related party, net | ||||||||
| Due to related parties (See Note 5) | ||||||||
| Accrued payroll due to officers | ||||||||
| Accrued interest to a related party | ||||||||
For the three months ended June 30, 2026 and 2025, we had the following related party transactions:
June 30, 2026 | June 30, 2025 | |||||||
| Net sales to a related party | $ | $ | ||||||
| Raw materials purchased from a related party | ||||||||
| Interest expense to a related party | ||||||||
| Other income | ||||||||
| Due from employee – related party, net | ||||||||
For the six months ended June 30, 2026 and 2025, we had the following related party transactions:
June 30, 2026 | June 30, 2025 | |||||||
| Net sales to a related party | $ | $ | ||||||
| Raw materials purchased from a related party | ||||||||
| Interest expense to a related party | ||||||||
| Other income | ||||||||
| Due from employee – related party, net | ||||||||
The
$
These transactions were not conducted at arm’s length and therefore may not reflect the terms that would have been agreed to with an unrelated third party.
14. RESEARCH SERVICES AGREEMENT WITH STEMSATION
On
July 1, 2024, the Company entered into a one-year Research Services Agreement with StemSation to provide research and development services
related to certain StemSation technologies. Under the agreement, the Company was entitled to receive $
15. SUBSEQUENT EVENTS
Convertible Promissory Notes
During July to August 2026, we issued convertible promissory notes to unrelated third parties for a total of $ with original issuance discount of $. The Noteholders have the right to convert the notes into shares of Common Stock at fixed conversion price ranging from $ to $ per share. The notes are due one year from the execution and funding of the notes. In connection with $ of the notes issued, we paid 10% of the proceeds to a third party, which has been recorded as a debt discount. Both the original issuance discount and the issuance-related costs are being amortized over the term of each note.
Promissory Notes
In
July 2026, the Company entered into a Purchase and Sale of Future Receipts Agreement with a third party. Pursuant to this agreement,
the buyer purchased $
Convertible Notes Receivable
During
August 2026, we purchased $
| F-27 |
Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
Introduction
Our business during the six months ended June 30, 2026 has focused upon marketing our homeopathic drugs for the treatment of pain:
| ● | Nyloxin (Stage 2 Pain) | |
| ● | Nyloxin Extra Strength (Stage 3 Pain) | |
| ● | Pet Pain–Away | |
| ● | Equine Pain–Away | |
| ● | Luxury Feet |
During the six months ended June 30, 2026 and thereafter, the following has occurred:
Since October of 2025, we have expanded our online efforts to include marketing and social media consultants to expand sales of Nyloxin and Pet Pain-Away. This has led to a bigger footprint on Amazon as well as the placement of Pet Pain-Away on Chewy, the largest online pet site.
During the second quarter of 2026, we have brought the Company’s financial reporting current.
Nyloxin/Nyloxin Extra Strength
We offer Nyloxin/Nyloxin Extra Strength as our over-the-counter (OTC) pain reliever that has been clinically proven to treat moderate to severe (Stage 2) chronic pain.
Nyloxin and Nyloxin Extra Strength are available as a two-ounce topical gel for treating joint pain and pain associated with arthritis and repetitive stress, and as a one ounce oral spray for treating lower back pain, migraines, neck aches, shoulder pain, cramps, and neuropathic pain. Both the topical gel and oral spray are packaged and sold as a one-month supply.
Nyloxin and Nyloxin Extra Strength offer several benefits as a pain reliever. With increasing concern about consumers using opioid and acetaminophen-based pain relievers, the Nyloxin products provide an alternative that does not rely on opiates or non-steroidal anti-inflammatory drugs, otherwise known as NSAIDs, for their pain-relieving effects. Nyloxin also has a well-defined safety profile. Since the early 1930s, the active pharmaceutical ingredient (API) of Nyloxin, Asian cobra venom, has been studied in more than 46 human clinical studies. The data from these studies provide clinical evidence that cobra venom provides an effective treatment for pain with few side effects and has the following benefits:
| ● | safe and effective; | |
| ● | all natural; | |
| ● | long-acting; | |
| ● | easy to use; | |
| ● | non-narcotic; | |
| ● | non-addictive; and | |
| ● | analgesic and anti-inflammatory. |
Potential side effects from the use of Nyloxin are rare, but may include headache, nausea, vomiting, sore throat, allergic rhinitis and coughing.
The primary difference between Nyloxin and Nyloxin Extra Strength is the dilution level of the venom. The approximate dilution levels for Nyloxin and Nyloxin Extra Strength are as follows:
Nyloxin
| ● | Topical Gel: 30 mcg/mL | |
| ● | Oral Spray: 70 mcg/mL |
Nyloxin Extra Strength
| ● | Topical Gel: 60 mcg/mL | |
| ● | Oral Spray: 140 mcg/mL |
In December 2011, we began marketing Nyloxin and Nyloxin Extra Strength at www.nyloxin.com. Both Nyloxin and Nyloxin Extra Strength are packaged in a roll-on container, squeeze bottle and as an oral spray. Additionally, Nyloxin topical gel is available in an 8 ounce pump bottle.
We are currently marketing Nyloxin and Nyloxin Extra Strength as treatments for moderate to severe chronic pain. Nyloxin is available as an oral spray for treating back pain, neck pain, headaches, joint pain, migraines, and neuralgia and as a topical gel for treating joint pain, neck pain, arthritis pain, and pain associated with repetitive stress. Nyloxin Extra Strength is available as an oral spray and gel application for treating the same physical indications but is aimed at treating the most severe (Stage 3) pain that inhibits one’s ability to function fully.
The Nyloxin products are available for sale on the www.Nyloxin.com website, the Nyloxin Amazon storefront at www.Amazon.com/nyloxin and on the Walmart Marketplace. Nyloxin is also sold in physician offices, clinics and small-chain pharmacies.
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Nyloxin Military Strength
In December 2012, we announced the availability of Nyloxin Military Strength for sale to the United States Military and Veteran’s Administration. Over the past few years, the U.S. Department of Defense has been reporting an increase in the use and abuse of prescription medications, particularly opiates. In 2009, close to 3.8 million prescriptions for pain relievers were written in the military. This staggering number was more than a 400% increase from the number of prescriptions written in the military in 2001. But prescription drugs are not the only issue. The most common and seemingly harmless way to treat pain is with non–steroidal, anti–inflammatory drugs (NSAIDS). But there are risks. Overuse can cause nausea, vomiting, diarrhea, heartburn, ulcers and internal bleeding. In severe cases chest pain, heart failure, kidney dysfunction and life–threatening allergic reactions can occur. It is reported that approximately 7,600 people in America die from NSAID use and some 78,000 are hospitalized. Ibuprofen, also an NSAID has been of particular concern in the military. The terms “Ranger Candy” and “Military Candy” refer to the service men and women who are said to use 800mg doses of Ibuprofen to control their pain. But when taking anti–inflammatory Ibuprofen in high doses for chronic pain, there is potential for critical health risks; abuse can lead to serious stomach problems, internal bleeding and even kidney failure. There are significantly greater health risks when abuse of this drug is combined with alcohol intake. Our goal is that with Nyloxin, we can greatly reduce the instances of opiate abuse and overuse of NSAIDS in high risk groups like the US military. The Nyloxin Military Strength represents the strongest version of Nyloxin available and is approximately twice as strong as Nyloxin Extra Strength. We are working with outside consultants to register Nyloxin Military Strength and the other Nyloxin products for sale to the US government and the various arms of the military as well as the Veteran’s Administration. In February of 2018, Nyloxin was added to the Federal Supply Schedule but was subsequently removed the following week without an adequate explanation. We have continued to work with our consultants to understand why our products were improperly removed the Federal Supply Schedule and when we may be able to get re-listed on the Federal Supply Schedule for eventual sales to governmental agencies or to the US Military.
International Sales
We are pursuing international drug registrations in Canada, Mexico, India, Australia, New Zealand, Central and South America and Europe. Since European rules for homeopathic drugs are different than the rules in the US, we cannot estimate when this process will be completed. On March 25, 2013 we announced the publication of our patent and trademark for Nyloxin in India. We are actively seeking new distribution partners in India. In December 2025, the Company entered into a business collaboration agreement with a third-party service provider to support its expansion into the Indian market. Under the agreement, the service provider will assist with business development activities, including identifying potential customers, facilitating negotiations, and supporting market entry efforts.
On May 14, 2015 we announced that we had engaged the Nature’s Clinic to begin the process of regulatory approval of our Company’s Over–the–Counter pain drug, Nyloxin for marketing and distribution in Canada. Due to lack of funding and then the subsequent COVID crisis, we have waited to complete the approval process to begin distributing Nyloxin and expect to re-engage in the process in 2026.
Additionally, we plan to complete several human clinical studies aimed at comparing the ability of Nyloxin Extra Strength to replace prescription pain relievers. We have provided protocols to several hospitals and will provide details and timelines when those protocols have been accepted. We cannot provide any timeline for these studies until adequate financing is available.
To date, our marketing efforts have been limited due to lack of funding. As sales increase, we plan to begin marketing more aggressively to increase the sales and awareness of our products.
Pet Pain–Away
During June of 2013, we announced the launch of our new homeopathic formula for the treatment of chronic pain in companion animals, Pet Pain–Away. Pet Pain–Away is a homeopathic, non–narcotic, non–addictive, over–the–counter pain reliever, primarily aimed at treating moderate to severe chronic pain in companion animals. It is specifically indicated to treat pain from hip dysplasia, arthritis pain, joint pain, and general chronic pain in dogs and cats. The initial product run was completed in December of 2014 and launched through Lumaxa Distributors on December 19, 2014.
In May of 2016, we signed a license agreement to begin the process of creating an infomercial (Direct Response) campaign for Pet Pain–Away. In November of 2016, we announced the license agreement with DEG Productions for the marketing and distribution of Pet Pain–Away globally. DEG created their own website (www.getpetpainaway.com) and began airing commercials in December of 2016.
In February of 2020, we took back the marketing of Pet Pain-Away and are currently selling the product on Amazon.com, Chewy.com, and www.petpainaway.com.
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Luxury Feet
In June of 2017, we announced the creation of Luxury Feet; an over–the–counter pain reliever and anti–inflammatory product that is designed for women who experience pain or discomfort due to high heels and stilettos. We announced the official marketing launch of Luxury Feet in March of 2021. The product is currently available through www.luxuryfeet.com and on Amazon.
Equine Pain-Away (Formerly Equine Nyloxin)
In October of 2013, we announced that we were in the process of launching the newest addition to our line of homeopathic treatments for chronic pain, Equine Nyloxin. We had been working with trainers and veterinarians in the equine industry and have already identified distributors for the product. The Equine Nyloxin represents the Company’s first topical solution for the animal market. Equine Nyloxin was rebranded as Equine Pain-Away™ and officially rolled into the market in October of 2019. Equine Pain-Away is being marketed through several retailers and online at www.EquinePainAway.com and on Amazon.
Drug Discovery and Pipeline
Nutra Pharma is developing proprietary therapeutic protein products for the biologics market. The Company has two leading drug candidates: RPI–MN and RPI–78M.
RPI–MN
RPI–MN inhibits the entry of several viruses that are known to cause severe neurological damage in such diseases as encephalitis and Human Immunodeficiency Virus (HIV). It is being developed first for the treatment of HIV.
RPI–78M
RPI–78M is being developed for the treatment of Multiple Sclerosis (MS) and Adrenomyeloneuropathy (AMN). Other neurological and autoimmune disorders that may be served by RPI–78M include Myasthenia Gravis (MG), Rheumatoid Arthritis (RA) and Amyotrophic Lateral Sclerosis (ALS).
RPI–78M and RPI–MN contain anticholinergic peptides that recognize the same receptors as nicotine (acetylcholine receptors) but have the opposite effect. In a specific chemical process unique to Nutra Pharma, the drugs are created through a process of chemical modification.
In September, 2015 RPI–78M was granted Orphan Status by the FDA for the treatment of pediatric Multiple Sclerosis. This allows for much shorter timelines to drug approval, waiver of FDA fees (around $2.5M), rolling review and fast–track approval. Orphan status also allows for potential grant money and other funding opportunities through the clinical process.
RPI–MN and RPI–78M possess several desirable properties as drugs:
● They lack measurable toxicity but are still capable of attaching to and affecting the target site on the nerve cells. This means that patients cannot overdose.
● They display no serious adverse side effects following years of investigations in humans and animals.
● They are extremely stable and resistant to heat, which gives the drugs a long shelf life. The drugs’ stability has been determined to be over 4 years at room temperature. This is extremely unusual for a biologic drug.
● RPI–78M may be administered orally –– a first for a biologic MS drug. This will present MS patients with additional quality of life benefits by eliminating the requirement for routine injections.
● They are easy to administer.
We are currently working with consultants to develop trial protocols for a Phase I/II trial for the use of RPI–78M in the treatment of Pediatric Multiple Sclerosis. Our goal is to initiate these trials in late 2026.
| 6 |
Critical Accounting Policies and Estimates
Our condensed consolidated unaudited financial statements and accompanying notes have been prepared in accordance with accounting principles generally accepted in the United States (“GAAP”) applied on a consistent basis. The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting periods. Our critical accounting policies and estimates are described in “Management’s Discussion and Analysis of Financial Condition and Results of Operations - Critical Accounting Policies and Estimates” in our Annual Report on Form 10-K filed with the SEC on May 20, 2026.
Effective January 1, 2026, the Company adopted ASU No. 2024-04, Debt—Debt with Conversion and Other Options (Subtopic 470-20): Accounting for Convertible Debt Instruments (“ASU 2024-04”), and ASU No. 2025-05, Financial Instruments—Credit Losses (Topic 326): Improvements to Credit Loss Guidance (“ASU 2025-05”). The adoption of these accounting standards did not have a material impact on the Company’s condensed consolidated financial statements.
Additionally, the Company evaluated the applicability of ASU No. 2023-07, Codification Improvements to Segment Reporting (Topic 280) (“ASU 2023-07”), which resulted in expanded segment disclosure requirements but did not materially impact the Company’s condensed consolidated financial statements.
We regularly evaluate the accounting policies and estimates that we use to prepare our unaudited condensed consolidated financial statements. In general, management’s estimates are based on historical experience, information from third party professionals, and various other assumptions that are believed to be reasonable under the facts and circumstances. Actual results could differ from those estimates made by management under different and/or future circumstances.
Results of Operations – Comparison of Three-Month Periods Ended June 30, 2026 and 2025
Net sales to unrelated customers were $34,463 for the three months ended June 30, 2026, compared to $84,532 for the same period in 2025, representing a decrease of $50,069, or approximately 59.23%. The decrease was primarily attributable to certain dietary supplement product lines that were transitioned to Avini Health beginning in the fourth quarter of 2025, while the Company retained ownership of its cobra venom technology and related individual brands, as well as lower private label customer order volumes and the timing of orders during the current quarter.
Net sales to a related party, Avini Health (Avini), were $23,459 for the three months ended June 30, 2026, compared to $37,611 for the same period in 2025, representing a decrease of $14,152, or approximately 37.63%. The decrease was primarily attributable to reduced sales volume during the current quarter compared to the prior-year period.
Cost of sales for the three–month period ended June 30, 2026 is $25,297 compared to $58,715, for the three–month period June 30, 2025. Our cost of sales includes the direct costs associated with manufacturing, shipping, handling costs, and inventory quality control personnel salaries. Our gross profit margin for the three–month period ended June 30, 2026 is $32,625 or 56.33% compared to $63,428 or 51.93% for the three–month period ended June 30, 2025. This gross margin includes reserves of $0 in the current quarter and $5,000 in the prior-year quarter for undelivered venom and slow-moving inventory. The slight increase was primarily attributable to lower manufacturing costs related to private label product sales to unrelated parties.
Operating expenses increased by $114,132, or 32.24%, from $353,957 for the quarter ended June 30, 2025 to $468,089 for the quarter ended June 30, 2026. The increase was primarily attributable to higher consulting fees related to general business advisory services and professional fees incurred in connection with the Company’s resumption of SEC filing and tax returns activities.
Other income was $2,305 and $8,750 for the three months ended June 30, 2026 and 2025, respectively. The increase was primarily attributable to $5,000 recognized during the second quarter of 2025 related to amounts received from a related party for the shared use of equipment.
Interest expense, including related party interest expense, increased $3,378 or 3.16%, from $106,792 for the quarter ended June 30, 2025 to $110,170 for the quarter ended June 30, 2026. This slight increase was primarily due to the increase in amortization of loan discounts in the quarter ended June 30, 2026 compared to the prior-year period.
We carry certain of our debentures at fair value. Due to the fact that the number of shares of common stock issuable could exceed the Company’s authorized share limit, the equity environment is tainted, and all additional convertible debt is included in the value of the derivative liabilities. For the three months ended June 30, 2026 and 2025, the liability related to these hybrid instruments fluctuated, resulting in a loss of $3,405,443 and a gain of $704,622, respectively. Interest expense on these debentures is included in the change in fair value of convertible notes and derivatives in the accompanying unaudited condensed consolidated statements of operations.
Gain on settlement of debt decreased by $53,526, from a gain of $53,526 the second quarter of 2025 to no gain or loss during the second quarter of 2026, primarily due to a gain recognized from a debt settlement executed during the second quarter of 2025.
As a result of the foregoing, our net loss increased by $4,318,349 or 1,168.46%, from a net income of $369,577 for the quarter ended June 30, 2025 to a net loss of $3,948,772 for the quarter ended June 30, 2026.
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Results of Operations – Comparison of Six-Month Periods Ended June 30, 2026 and 2025
Net sales to unrelated customers were $61,709 for the six months ended June 30, 2026, compared to $158,506 for the same period in 2025, a decrease of $96,797, or approximately 61.07%. The decrease was primarily attributable to certain dietary supplement product lines that were transitioned to Avini Health beginning in the fourth quarter of 2025, while the Company retained ownership of its cobra venom technology and related individual brands, as well as lower private label customer order volumes and the timing of orders during the current quarter.
Net sales to a related party, Avini Health (Avini), were $44,427 for the six months ended June 30, 2026, compared to $74,031 for the same period in 2025—a decrease of $29,604, or approximately 39.99%. The decrease was primarily attributable to reduced sales volume during the current quarter compared to the prior-year period.
Cost of sales for the six–month period ended June 30, 2026 is $54,536 compared to $104,978 for the six–month period June 30, 2025. Our cost of sales includes the direct costs associated with manufacturing, shipping and handling costs. Gross profit for the six months ended June 30, 2026 was $51,600, or 48.62%, compared to $122,559, or 52.71%, for the comparable period in 2025. Gross profit in prior-year period includes inventory reserves of $5,000 related to undelivered venom and slow-moving inventory. Excluding these reserves, gross margin for the six months ended June 30, 2026 would have been approximately 48.62%, compared to 54.86% for the prior-year period. The decrease in adjusted gross margin is primarily attributable to higher manufacturing costs associated with private label product sales to unrelated parties, reflecting a different product mix during the six-month period.
Operating expenses increased by $103,406, or 13.55%, from $762,907 for the six months ended June 30, 2025 to $866,313 for the six months ended June 30, 2026. The increase was primarily attributable to higher professional fees incurred in connection with the Company’s resumption of SEC filing and tax returns activities.
Other income totaled $2,305 and $58,750 for the six months ended June 30, 2026 and 2025, respectively. Amounts in prior-year period was primarily attributable to $50,000 recognized in the first quarter of 2025 under a short-term research and development services contract, and $5,000 related to a one-time related-party reimbursement for shared equipment usage recognized in the second quarter of 2025.
Interest expense, including related party interest expense, increased $5,945 or 2.91%, from $204,587 for the six months ended June 30, 2025 to $210,532 for the six months ended June 30, 2026. This increase was primarily due to the increase in amortization of loan discounts in the six months ended June 30, 2026 compared to the six months ended June 30, 2025.
We carry certain of our debentures and common stock warrants at fair value. Due to the fact that the number of shares of common stock issuable could exceed the Company’s authorized share limit, the equity environment is tainted, and all additional convertible debt, options and warrants are included in the value of the derivative liabilities. For the six months ended June 30, 2026 and 2025, the liability related to these hybrid instruments fluctuated, resulting in a loss of $3,526,007 and $302,687, respectively. Interest expense on these debentures is included in the change in fair value of convertible notes and derivatives in the accompanying unaudited condensed consolidated statements of operations.
Gain on settlement of debt and accrued expenses for the six months ended June 30, 2026 was $140,500, compared to a gain of $53,526 for the corresponding period in 2025. The higher gain in 2026 was primarily attributable to differences in the terms and resulting gains recognized on debt settlements during the respective periods.
As a result of the foregoing, our net loss increased by $3,373,101 or 325.79%, from net loss of $1,035,346 for the six months ended June 30, 2025 to a net loss of $4,408,447 for the six months ended June 30, 2026.
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Liquidity and Capital Resources
We have incurred significant losses from operations and working capital and stockholders’ deficits raise substantial doubt about our ability to continue as a going concern. Further, as stated in Note 1 to our condensed consolidated unaudited financial statements for the period ended June 30, 2026, we have an accumulated deficit of $82,686,976 at June 30, 2026. In addition, we have a significant amount of indebtedness in default, a working capital deficit of $21,233,689 and a stockholders’ deficit of $21,208,753 at June 30, 2026.
Our ability to continue as a going concern is contingent upon our ability to secure additional financing, increase ownership equity, and attain profitable operations. In addition, our ability to continue as a going concern must be considered in light of the problems, expenses and complications frequently encountered in established markets and the competitive environment in which we operate. As of the date of the filing of this report, we do not believe that our source of cash is adequate for the next 12 months of operation and there is substantial doubt about our ability to continue as a going concern. In addition, our common stock is presently on the OTC Market Group’s Expert Market, which means that the Company’s common stock is not eligible for proprietary broker-deal quotes.
Current operations are primarily being funded through a combination of product sales, promissory notes and convertible notes. During the six months ended June 30, 2026, the Company raised $463,001 from the issuance of convertible notes and $83,250 from promissory notes.
The Company will require additional capital to manufacture Nyloxin and Pet Pain–Away and to reduce our debt level. We estimate that we will require approximately $1,200,000 to fund our existing operations over the next twelve months. These costs include: (i) compensation for six (6) full-time employees; (ii) compensation for various consultants who we deem critical to our business; (iii) general office expenses including rent and utilities; (iv) product liability insurance; and (v) outside legal and accounting services. These costs reflected in (i) – (v) do not include research and development costs or other costs associated with clinical studies.
Our ability to meet our future operating expenses is highly dependent on the amount of such future revenues. To the extent that future revenues from the sales of Nyloxin and Pet Pain-Away are insufficient to cover our operating expenses we may need to raise additional equity capital, which could result in substantial dilution to existing shareholders. There can be no assurance that we will be able to raise sufficient equity capital to fund our working capital requirements on terms acceptable to us, or at all. We may also seek additional loans from our officers and directors; however, there can be no assurance that we will be successful in securing such additional loans.
The accompanying Unaudited Condensed Consolidated Financial Statements do not include any adjustments relating to the recoverability and classification of recorded asset amounts or the amounts and classification of liabilities that might be necessary should we be unable to continue as a going concern.
Uncertainties and Trends
Our operations and possible revenues are dependent now and in the future upon the following factors:
| ● | Whether we successfully develop and commercialize products from our research and development activities. | |
| ● | If we fail to compete effectively in the intensely competitive biotechnology area, our operations and market position will be negatively impacted. | |
| ● | If we fail to successfully execute our planned partnering and out-licensing of products or technologies, our future performance will be adversely affected. | |
| ● | The recent economic downturn and related credit and financial market crisis may adversely affect our ability to obtain financing, conduct our operations and realize opportunities to successfully bring our technologies to market. | |
| ● | Biotechnology industry related litigation is substantial and may continue to rise, leading to greater costs and unpredictable litigation. | |
| ● | If we fail to comply with extensive legal/regulatory requirements affecting the healthcare industry, we will face increased costs, and possibly penalties and business losses. |
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Off–Balance Sheet Arrangements
We have not entered into any transaction, agreement or other contractual arrangement with an entity unconsolidated with us under whom we have:
| ● | An obligation under a guarantee contract. | |
| ● | A retained or contingent interest in assets transferred to the unconsolidated entity or similar arrangement that serves as credit, liquidity or market risk support to such entity for such assets. | |
| ● | Any obligation, including a contingent obligation, under a contract that would be accounted for as a derivative instrument. | |
| ● | Any obligation, including a contingent obligation, arising out of a variable interest in an unconsolidated entity that is held by us and material to us where such entity provides financing, liquidity, market risk or credit risk support to, or engages in leasing, hedging or research and development services with us. |
We do not have any off-balance sheet arrangements or commitments that have a current or future effect on its financial condition, changes in financial condition, revenues or expenses, results of operations, liquidity, capital expenditures, or capital resources that is material, other than those which may be disclosed in this Management’s Discussion and Analysis of Financial Condition and the unaudited Condensed Consolidated Financial Statements and related notes.
Item 3. Quantitative and Qualitative Disclosures About Market Risk
Not applicable
Item 4. Controls and Procedures
Disclosure Controls and Procedures
As of June 30, 2026, we carried out an evaluation under the supervision and the participation of our Chief Executive Officer, of the effectiveness of our disclosure controls and procedures as of June 30, 2026, as defined in Rule 13a–15 under the Securities Exchange Act of 1934 (“Exchange Act”). Based on that evaluation, our management, including our Chief Executive Officer, concluded that, because of the material weaknesses in internal control over financial reporting discussed in Section 9A of our annual report on Form 10–K, our disclosure controls and procedures were not effective, at a reasonable assurance level, as of June 30, 2026. In light of this, we performed additional post–closing procedures and analyses in order to prepare the Condensed Consolidated Unaudited Financial Statements included in this report. As a result of these procedures, we believe our Condensed Consolidated Unaudited Financial Statements included in this report present fairly, in all material respects, our financial condition, results of operations and cash flows for the periods presented. A control system cannot provide absolute assurance, however, that the objectives of the controls system are met, and no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, with the company have been detected.
Disclosure controls and procedures are controls and other procedures that are designed to ensure that information required to be disclosed in our reports filed or submitted under the Exchange Act is recorded, processed, summarized and reported, within the time periods specified in the Securities and Exchange Commission’s rules and forms. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed in our reports filed under the Exchange Act is accumulated and communicated to management, including our Chief Executive Officer, who also acted as our Principal Financial Officer as appropriate, to allow timely decisions regarding required disclosure.
Changes in Internal Control over Financial Reporting
There were no changes in our internal control over financial reporting identified in connection with the evaluation required by paragraph (d) of Rule 13a–15 or 15d–15 under the Exchange Act that occurred during the six months ended June 30, 2026 that have materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
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PART II. OTHER INFORMATION
Item 1. Legal Proceedings
Marc Weller v. Nutra Pharma Corporation, Case No. CACE-24-018346
In January 2026, the Company entered into a settlement agreement with Marc Weller resolving litigation in Broward County, Florida. Pursuant to the settlement, the Company agreed to cancel and extinguish outstanding notes with an aggregate carrying value of approximately $172,500 in exchange for $20,000 in cash, which was fully repaid in installments through April 2026, and the issuance of 60 million shares of common stock.
CSA 8411, LLC v. Nutra Pharma Corp., Case No. CACE 18-023150
On October 12, 2018, CSA 8411, LLC filed a lawsuit against the Company in the 17th Judicial Circuit Court in and for Broward County, Florida (Case No. CACE 18-023150) to recover $100,000 allegedly owed under an amended promissory note dated April 12, 2017. The Company filed its Answer and Affirmative Defenses on November 1, 2018, and asserted counterclaims against the plaintiff and certain related parties. Mediation was held on June 21, 2019 but did not result in a resolution at that time. The dispute remained ongoing until it was resolved through settlement in May 2025.
On May 19, 2025, the parties settled the case; fully resolving all existing disputes and conflicts between the parties. We agreed to pay $35,000 to the plaintiff(s) on or before May 19, 2025 and completed nine monthly payments of $10,000 each, with all amounts paid in full as of February 2026. The case was dismissed on May 20, 2025 and all payments have been made as agreed.
Securities and Exchange Commission v. Nutra Pharma Corporation, Erik Deitsch, and Sean Peter McManus
On September 28, 2018, the United States Securities and Exchange Commission (the “SEC”) filed a lawsuit in the United States District Court for the Eastern District of New York (Case No. 2:18-cv-05459) against the Company, Mr. Deitsch, and Mr. McManus. The lawsuit alleges that, from July 2013 through June 2018, the Company and the other defendants’ defrauded investors by making materially false and misleading statements about the Company and violated anti-fraud and other securities laws.
The violations alleged against the Company by the SEC include: (a) raising over $920,000 in at least two private placement offerings for which the Company failed to file required registration statements with the SEC; (b) issuing a series of materially false or misleading press releases; (c) making false statements in at least one Form 10-Q; and (d) failing to make required public filings with the SEC to disclose the Company’s issuance of millions of shares of stock. The lawsuit makes additional allegations against Mr. McManus and Mr. Deitsch, including that Mr. McManus acted as a broker without SEC registration and defrauded at least one investor by making false statements about the Company, that Mr. Deitsch engaged in manipulative trades of the Company’s stock by offering to pay more for shares he was purchasing than the amount the seller was willing to take, and that Mr. Deitsch failed to make required public filings with the SEC. The lawsuit seeks both injunctive and monetary relief.
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On May 29, 2019 (following each of the defendants filing motions to dismiss), the SEC filed a First Amended Complaint which generally alleged the same conduct as its original Complaint, but accounted for certain guidance provided by the United States Supreme Court in a case that had been recently decided. Each of the defendants then moved to dismiss the SEC’s First Amended Complaint. On June 30, 2020, the Court entered an Order granting in part and denying in part the various motions to dismiss. Following that Order, the SEC filed a Second Amended Complaint (the operative pleading) and the defendants filed their answers which generally denied liability. The Court conducted a hearing on February 23, 2021 and set an initial briefing schedule for the SEC’s Motion for Partial Summary Judgment wherein the Plaintiffs’ Motion for Partial Summary Judgment was due on April 5, 2021, the Defendants’ Consolidated (i.e., collectively, Nutra Pharma Corporation, Erik “Rik” Deitsch, and Sean McManus) Response Brief to the SEC’s Motion was due May 3, 2021, and the Plaintiffs’ Reply Brief was due on May 19, 2021. On March 23, 2021, the Plaintiff filed a Motion for Extension of Time to file the Motion for Partial Summary Judgment. On April 9, 2021, the Plaintiff filed a Motion for Partial Summary Judgment, Defendants’ filed a Memorandum of Law in Opposition to Plaintiff’s Motion on May 7, 2021, and Plaintiff filed its Reply brief on May 21, 2021.
In July 2024, a final judgment was issued, ordering the defendant to pay $520,940 in disgorgement, $59,295 in prejudgment interest, and a $100,000 civil penalty. As of June 30, 2026 and December 31, 2025, the Company had accrued a total legal settlement amount of $680,235.
Item 2. Unregistered Sales of Equity Securities and Use of Proceeds
During January through April 2026, the Company issued 110,000,000 shares of its common stock to two service providers pursuant to consulting agreements. These shares have been recorded as common stock to be issued, as the transfer agent had not yet completed the issuance process.
During January 2026, the Company issued 60,000,000 shares of common stock in connection with the settlement and extinguishment of convertible notes payable with an aggregate carrying value of $172,500.
Item 3. Defaults Upon Senior Securities
As of June 30, 2026, certain of the Company’s promissory notes and convertible promissory notes were in default. The Company is currently negotiating settlements with the respective noteholders. Additional information regarding these notes is included in Note 6 – Debt Notes to the unaudited condensed consolidated financial statements included in Part I of this report.
Item 4. Mine Safety Disclosures
Not applicable.
Item 5. Other Information
None
Item 6. Exhibits
| Exhibit No. | Title | |
| 31.1 | Certification of Chief Executive Officer and Chief Financial Officer pursuant to Section 302 of the Sarbanes–Oxley Act of 2002. | |
| 32.1 | Certification of Chief Executive Officer and Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes–Oxley Act of 2002. | |
| 101.INS | Inline XBRL Instance Document | |
| 101.SCH | Inline XBRL Taxonomy Extension Schema Document | |
| 101.CAL | Inline XBRL Taxonomy Extension Calculation Linkbase Document | |
| 101.DEF | Inline XBRL Taxonomy Extension Definition Linkbase Document | |
| 101.LAB | Inline XBRL Taxonomy Extension Label Linkbase Document | |
| 101.PRE | Inline XBRL Taxonomy Extension Presentation Linkbase Document | |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document) |
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SIGNATURES
In accordance with the requirements of the Securities Exchange Act of 1934, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
| NUTRA PHARMA CORP. | |
| Registrant | |
| Dated: August 19, 2026 | /s/ Michael Flax, DDS |
| Michael Flax, DDS | |
| Chief Executive Officer/Chief Financial Officer |
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