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Sonoma Pharmaceuticals, Inc. SNOA US Equity

Health Care · CIK 1367083 · FY ends Mar 31
$1.31
-0.02 (-1.50%)
USD · as of 2026-08-28 · marketstack

Sonoma Pharmaceuticals, Inc. (Nasdaq: SNOA), an SEC filer in Surgical & Medical Instruments & Apparatus, closed at $1.31, -1.5%, on 2026-08-28, with a market cap of $6M, a return on equity of -84.6%, a net margin of -16.3% and 3-year sales growth of 13.7%. Institutional ownership, earnings history and filed financials are on the tabs below.

SNOA · 10-K · period ended 2022-03-31

← all SNOA documents
filed 2022-07-13 · EDGAR original ↗

Our rendering of the filing — original pagination and typography are not reproduced, and tables are reduced to their short label cells (the figures live on FA). Nothing is summarized: every line below is the filing's own text.

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ITEM 7. Management’s Discussion

and Analysis of Financial Condition and Results of Operations

Critical Accounting Policies

The preparation of our consolidated financial

statements in conformity with accounting principles generally accepted in the United States of America requires management to exercise

its judgment. We exercise considerable judgment with respect to establishing sound accounting policies and in making estimates and assumptions

that affect the reported amounts of our assets and liabilities, our recognition of revenues and expenses, and disclosure of commitments

and contingencies at the date of the consolidated financial statements.

On an ongoing basis, we evaluate our estimates

and judgments. Areas in which we exercise significant judgment include, but are not necessarily limited to, our valuation of accounts

receivable, inventory, income taxes, equity transactions (compensatory and financing) and contingencies.

We base our estimates and judgments on a variety

of factors including our historical experience, knowledge of our business and industry, current and expected economic conditions, the

attributes of our products, the regulatory environment, and in certain cases, the results of outside appraisals. We periodically re-evaluate

our estimates and assumptions with respect to these judgments and modify our approach when circumstances indicate that modifications are

necessary.

While we believe that the factors we evaluate

provide us with a meaningful basis for establishing and applying sound accounting policies, we cannot guarantee that the results will

always be accurate. Since the determination of these estimates requires the exercise of judgment, actual results could differ from such

estimates.

For a Summary of Critical Accounting Policies,

please refer to Notes to Consolidated Financial Statements, Note 3.

Results of Continuing Operations

Comparison of the Year Ended March 31, 2022

and 2021

Revenue

The following table shows our consolidated total

revenue and revenue by geographic region for the year ended March 31, 2022 and 2021:

Years Ended March 31,

(In thousands) 2022 2021 $ Change % Change

The decrease in United States revenues for the

year ended March 31, 2022 compared to the same period in the prior year of $1.6 million, is primarily the result of our transition from

a direct sales force to a distributor model for our dermatology and eye care prescription products in the United States. Under the old

direct sales model, our revenues were higher due to higher retail pricing than what we agreed to with the distributors. However, our operating

expenses are also much lower under this new arrangement as we do not have to manage a sales force, provide patient rebates or manage product

substitutions. Revenue for our animal health products declined slightly. Revenue for wound care products increased 19% from the prior

year.

As a result of the asset purchase agreement and

arrangement we entered into on October 27, 2016 with Invekra,with our assistance Invekra built up their own manufacturing of HOCl products

and we manufactured products for Invekra at cost during the transition time. Invekra began their own manufacturing in November 2020. As

we previously disclosed, we expected our revenues to decline following the transition of Invekra towards their own manufacturing. Since

November 2020, we continue to process overflow orders for Invekra but we do so at market prices and at lower volumes. As a result of the

foregoing, Latin America revenue declined by $3.9 million during the year ended March 31, 2022 compared to the year ended March 31, 2021.

The decrease in Europe and Rest of the World revenues

for the year ended March 31, 2022 compared to the prior year was primarily the result of decreases in disinfectant sales in the Middle

East due to the pandemic receding and to a lesser extent a slight decline in European sales.

Cost of Revenue and Gross Profit

The cost of revenue and gross profit metrics are

as follows:

Year ended March 31,

(In thousands, except for percentages) 2022 2021 Change % Change

Cost of Revenue as a % of Revenue 68% 65% 3%

Gross Profit as a % of Revenue 32% 35% (3)%

The gross margin decrease of 3% for the year ended

March 31, 2022 compared to the year ended March 31, 2021 is a result of product mix and higher sales to distributors versus sales through

our direct sales force.

Research and Development Expense

The research and development metrics are as follows:

Year ended March 31,

(In thousands, except for percentages) 2022 2021 Change % Change

Research and Development Expense $ 125 $ 555 $ (430 ) (77)%

Research and Development Expense as a % of Revenue 1% 3% (2)%

For the year ended March 31, 2022, research and

development expenses decreased as a result the closure of our research and development facility in Seattle, Washington and its relocation

to our facility in Mexico.

Selling, General and Administrative Expense

The selling, general and administrative expense

metrics are as follows:

Year ended March 31,

(In thousands, except for percentages) 2022 2021 Change % Change

Selling, General and Administrative Expense $ 9,755 $ 9,453 $ 302 3%

Selling, General and Administrative Expense as a % of Revenue 77% 50% 27%

The increase in Selling, General and Administrative

expense for the year ended March 31, 2022 was primarily the result of an increase in our insurance premiums.

Interest (Expense) Income, net

Interest (expense) income, net was $(10,000) and

$4,000, respectively, for the years ended March 31, 2022 and March 31, 2021.

Forgiveness of PPP loan

On May 1,

2020, we received loan proceeds in the amount of $1,310,000 under the Paycheck Protection Program (“PPP”), from Coastal

States Bank in Atlanta, Georgia. We used the loan amount for eligible purposes, such as payroll expenses. For the year ended March 31,

2022, we received approval for loan forgiveness in the amount of $723,000.

Other Expense, net

Other expense, net for the year ended March 31,

2022 and 2021, was $394,000 and $594,000, respectively. The decrease in other expense, net relates primarily to a reduction in foreign

exchange losses.

Gain on Sale of Assets

For the year ended March 31, 2022, we sold equipment

for a gain of $150,000. Gain on the sale of assets for the year ended March 31, 2021 was $137,000. We sold fixed assets no longer needed

after closing our Petaluma manufacturing facility.

Income Tax Benefit (Expense)

Income tax benefit (expense) for the year ended

March 31, 2022 was $332,000 compared to $(713,000) for the year ended March 31, 2021. The increase in income tax benefit is the result

of the reversal of the valuation allowance for Mexico as the result of three years of taxable income.

Net Loss from Continuing Operations

Net loss from continuing operations for the year

ended March 31, 2022 and 2021, was $5,086,000 and $4,615,000, respectively.

Results of Discontinued Operations

Comparison of Year ended March 31, 2022 and 2021

On June 24, 2020, we closed on an asset purchase

agreement with Infinity Labs SD, Inc. We decided to divest our Micromed business, resulting in a strategic shift that had a major effect

on our operations and financial results. Therefore, the divested Micromed operations meet the criteria to be reported as discontinued

operations.

The related assets, liabilities, results of operations

and cash flows for our Micromed business are classified as discontinued operations for all periods presented.

The operations of the Micromed business included in discontinued operations

is summarized as follows:

Year ended March 31,

Selling general and administrative expenses – 38,000

Income from discontinued operations before tax – 123,000

Gain on disposal of discontinued operations before income taxes – 770,000

Total income from discontinued operating, before tax – 893,000

Income Tax benefit (expense) – (228,000 )

Income from discontinued operations, net of tax $ – $ 665,000

Gain on disposal of discontinued operations for

the year ended March 31, 2021, includes $770,000 of gain primarily from the value of the customer base of Micromed partially offset by

a working capital adjustment.

Net Loss

The following table provides the net loss for

each period along with the computation of basic and diluted net income per share:

For the Year Ended March 31,

(In thousands, except per share data) 2022 2021

Numerator:

Loss from continuing operations $ (5,086 ) $ (4,615 )

Income from discontinued operations – 665

Denominator:

Loss per share from continuing operations $ (1.92 ) $ (2.31 )

Income per share from discontinued operations – 0.33

Net loss per share: basic and diluted $ (1.92 ) $ (1.97 )

Liquidity and Capital Resources

We reported a net loss of $5,086,000 and $3,950,000

for the years ended March 31, 2022 and 2021, respectively. At March 31, 2022 and 2021, our accumulated deficit amounted to $184,363,000

and $179,277,000, respectively. As of March 31, 2022, we had cash and cash equivalents of $7,396,000 compared to $4,220,000 on March 31,

2021. Since our inception, substantially all of our operations have been financed through sales of equity securities. Other sources of

financing that we have used to date include our revenues, as well as various loans and the sale of certain assets to Invekra, Petagon,

MicroSafe and Infinity Labs.

Since April 1, 2021, substantially all of our

operations have been financed through the following transactions:

· Proceeds of $7,554,000 from sales on the ATM facility with HC Wainwright; and

· Proceeds of $217,000 from the exercise of stock options and warrants

The following table presents a summary of our

consolidated cash flows for operating, investing and financing activities for the year ended March 31, 2022 and 2021 as well balances

of cash and cash equivalents and working capital:

Year ended March 31,

Net cash provided by (used in):

Operating activities $ (4,248 ) $ (3,378 )

Investing activities (99 ) 388

Effect of exchange rates on cash 127 211

Net change in cash and cash equivalents 3,176 529

Cash and cash equivalents, beginning of the period 4,220 3,691

Cash and cash equivalents, end of the period $ 7,396 $ 4,220

Working capital (1), end of period $ 10,611 $ 8,905

(1) Defined as current assets minus current liabilities.

As of March 31, 2022, we had cash and cash equivalents

of $7,396,000 compared to $4,220,000 as of March 31, 2021.

Net cash used in operating activities during the

year ended March 31, 2022 was $4,248,000, primarily due to a net loss of $5,086,000 and partially offset by an increase from accounts

receivable net provision for write-offs and returns and an increase of $900,000 from deferred revenue.

Net cash used in operating activities during the

year ended March 31, 2021 was $3,378,000, primarily due to a net loss of $3,950,000 for the period.

Net cash used in investing activities for the

year ended March 31, 2022 was $99,000, primarily related to the purchase of property and equipment.

Net cash provided by investing activities for

the year ended March 31, 2021 was $388,000, primarily related to the proceeds from the sale of our Micromed division of $610,000 partially

offset by the purchase of equipment.

Net cash provided by financing activities for

the year ended March 31, 2022 was $7,396,000 primarily related to proceeds of $7,554,000 from the sale of common stock on our At-the-Market

facility with HC Wainwright, proceeds of $216,000 from the exercise of stock options and warrants, partially offset by the payments on

PPP loan and long term debt.

Net cash provided by financing activities for

the year ended March 31, 2021 was $3,308,000, primarily related to proceeds from the exercise of stock options and warrants of $2,287,000,

and PPP loans of $1,310,000 partially offset by payments on long term debt.

We expect revenues to fluctuate and may incur

losses in the foreseeable future and may need to raise additional capital to pursue our product development initiatives, to penetrate

markets for the sale of our products and continue as a going concern. We cannot provide any assurances that we will be able to raise additional

capital.

Management believes that we have access to capital

resources through possible public or private equity offerings, debt financings, corporate collaborations or other means; however, we cannot

provide any assurance that new financing will be available on commercially acceptable terms, if at all. If the economic climate in the

U.S. deteriorates, our ability to raise additional capital could be negatively impacted. If we are unable to secure additional capital,

we may be required to take additional measures to reduce costs in order to conserve our cash in amounts sufficient to sustain operations

and meet our obligations. These measures could cause significant delays in our continued efforts to commercialize our products, which

is critical to the realization of our business plan and our future operations. These matters raise substantial doubt about our ability

to continue as a going concern.

Capital Expenditures

We currently forecast capital expenditures in

order to execute on our business plan and maintain growth; however, the actual amount and timing of such capital expenditures will ultimately

be determined by the volume of business. We currently do not anticipate that a material amount will be purchased for the year ended March

31, 2023. If we purchase capital equipment, we expect to pay cash for those expenditures or to finance them through equipment leases.

Material Trends and Uncertainties

We are exposed to risk from decline in foreign

currency for both the Euro and the Mexico Peso versus the US dollar. Most recently there has been a sharp decline in the Euro versus the

US Dollar which has impacted our financial results.

As we have previously

discussed in our annual report on Form 10-K filed with the SEC on July 14, 2021, we face a substantial Mexico tax liability, intercompany

debt, unpaid technical assistance charges and accrued interest. These amounts are not due until 2027. At this time, management believes

there are sufficient assets on the balance sheet to more than cover any tax obligation without interrupting the Company’s operations

or business. We have engaged tax professionals to review all options to limit our exposure to these amounts and to proceed in a manner

that is most advantageous to the Company.

As the pandemic continues

to impact economies worldwide, we are closely watching inflation, increased volatility within financial markets, shipping costs, supply

chain issues and labor costs. At this time, the overall impact of these issues has been minimal. The potential impact to our business

operations, customer demand and supply chain due to increased shipping costs may ultimately impact sales. We continue to evaluate our

end-to-end supply chain and assess opportunities to refine the impact on sales. Currently, most of our customers pay for shipping expenses,

including increased shipping costs, if any. We have not yet faced labor shortages however it is possible we may have difficulties retaining

and finding qualified employees in a tight labor market in the future. Furthermore, overall inflation tendencies may put pressure on our

product pricing and/or costs.

We also closely monitor

overall economic conditions and consumer sentiment and the prospect of a recession in the United States which may impact our financial

results.

Use of Estimates

The preparation of consolidated financial statements

in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions

that affect the reported amounts of assets and liabilities and disclosures of contingent liabilities at the dates of the consolidated

financial statements and the reported amounts of revenues and expenses during the reporting periods. Actual results could differ from

these estimates. Significant estimates and assumptions include reserves and write-downs related to receivables and inventories, the recoverability

of long-lived assets, the valuation allowance related to our deferred tax assets, valuation of equity and derivative instruments, debt

discounts, valuation of investments and the estimated amortization periods of upfront product licensing fees received from customers.

Off-Balance Sheet Transactions

We currently have no off-balance sheet arrangements

that have or are reasonably likely to have a current or future material effect on our financial condition, changes in financial condition,

revenues or expenses, results of operations, liquidity, capital expenditures or capital resources.

ITEM 7A. Quantitative and Qualitative Disclosures About

Market Risk

As a smaller reporting company as defined by Rule 12b-2

of the Exchange Act and in Item 10(f)(1) of Regulation S-K, we are electing scaled disclosure reporting obligations and therefore

are not required to provide the information requested by this Item.

ITEM 8. Consolidated Financial Statements and Supplementary

Data

Sonoma Pharmaceuticals, Inc.

Index to Consolidated Financial Statements

Page

Report of Independent Registered Public Accounting Firm (PCAOB No. 215) F-1

Report of Independent Registered Public Accounting Firm (PCAOB No. 688) F-2

Consolidated Balance Sheets as of March 31, 2022 and 2021 F-4

Notes to Consolidated Financial Statements F-8

REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING

FIRM

To the Shareholders and Board of Directors of Sonoma Pharmaceuticals,

Inc.

Opinion on the Consolidated Financial Statements

We have audited the accompanying consolidated balance sheet of Sonoma

Pharmaceuticals, Inc. and Subsidiaries (the "Company") as of March 31, 2022, and the related consolidated statements of comprehensive

loss, changes in stockholders' equity and cash flows for the year ended March 31, 2022, and the related notes (collectively referred to

as the consolidated financial statements). In our opinion, the consolidated financial statements present fairly, in all material respects,

the financial position of the Company as of March 31, 2022, and the results of their operations and cash flows for the year ended March

31, 2022, in conformity with accounting principles generally accepted in the United States of America.

Substantial Doubt About the Company’s Ability to Continue

as a Going Concern

The accompanying consolidated financial statements have been prepared

assuming that the Company will continue as a going concern. As discussed in Note 2 to the financial statements, the Company has incurred

significant losses and needs to raise additional funds to meet its obligations and sustain its operations. These conditions raise substantial

doubt about its ability to continue as a going concern. Management's plans in regard to these matters are also described in Note 2. The

consolidated financial statements do not include any adjustments that might result from the outcome of this uncertainty.

Basis for Opinion

These consolidated financial statements are the responsibility of the

Company's management. Our responsibility is to express an opinion on the Company's consolidated financial statements based on our audit.

We are a public accounting firm registered with the Public Company Accounting Oversight Board (United States) (“PCAOB”) and

are required to be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules

and regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audit in accordance with the standards of the PCAOB.

Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the consolidated financial statements

are free of material misstatement, whether due to error or fraud. The Company is not required to have, nor were we engaged to perform,

an audit of its internal control over financial reporting. As part of our audit we are required to obtain an understanding of internal

control over financial reporting but not for the purpose of expressing an opinion on the effectiveness of the Company's internal control

over financial reporting. Accordingly, we express no such opinion.

Our audit included performing procedures to assess the risks of material

misstatement of the financial statements, whether due to error or fraud, and performing procedures that respond to those risks. Such procedures

included examining, on a test basis, evidence regarding the amounts and disclosures in the consolidated financial statements. Our audit

also included evaluating the accounting principles used and significant estimates made by management, as well as evaluating the overall

presentation of the consolidated financial statements. We believe that our audit provides a reasonable basis for our opinion.

Critical Audit Matters

Critical audit matters are matters arising from the current period

audit of the consolidated financial statements that were communicated or required to be communicated to the audit committee and that:

(1) relate to accounts or disclosures that are material to the consolidated financial statements and (2) involved our especially challenging,

subjective, or complex judgments. We determined that there are no critical audit matters.

/s/ Frazier & Deeter, LLC

We have served as the Company's auditor since 2021.

Atlanta, Georgia

July 13, 2022

REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING

FIRM

To the Shareholders and Board of Directors of

Sonoma Pharmaceuticals, Inc.

Opinion on the Financial Statements

We have audited the accompanying consolidated

balance sheet of Sonoma Pharmaceuticals, Inc. and Subsidiaries (the “Company”) as of March 31, 2021, the related consolidated

statements of comprehensive loss, changes in stockholders’ equity and cash flow for the year ended March 31, 2021 , and the

related notes (collectively referred to as the “financial statements”). In our opinion, the financial statements present fairly,

in all material respects, the financial position of the Company as of March 31, 2021, and the results of its operations and its cash flow

for the year ended March 31, 2021, in conformity with accounting principles generally accepted in the United States of America.

Explanatory Paragraph – Going Concern

The accompanying consolidated financial statements

have been prepared assuming that the Company will continue as a going concern. As more fully described in Note 2, the Company has incurred

significant losses and needs to raise additional funds to meet its obligations and sustain its operations. These conditions raise substantial

doubt about the Company's ability to continue as a going concern. Management's plans in regard to these matters are also described in

Note 2. The consolidated financial statements do not include any adjustments that might result from the outcome of this uncertainty.

Basis for Opinion

These financial statements are the responsibility

of the Company's management. Our responsibility is to express an opinion on the Company's financial statements based on our audit. We

are a public accounting firm registered with the Public Company Accounting Oversight Board (United States) ("PCAOB") and are

required to be independent with respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and

regulations of the Securities and Exchange Commission and the PCAOB.

We conducted our audit in accordance with the

standards of the PCAOB. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial

statements are free of material misstatement, whether due to error or fraud. The Company is not required to have, nor were we engaged

to perform, an audit of its internal control over financial reporting. As part of our audit we are required to obtain an understanding

of internal control over financial reporting but not for the purpose of expressing an opinion on the effectiveness of the Company's internal

control over financial reporting. Accordingly, we express no such opinion.

Our audit included performing procedures to assess

the risks of material misstatement of the financial statements, whether due to error or fraud, and performing procedures that respond

to those risks. Such procedures included examining, on a test basis, evidence regarding the amounts and disclosures in the financial statements.

Our audit also included evaluating the accounting principles used and significant estimates made by management, as well as evaluating

the overall presentation of the financial statements. We believe that our audit provides a reasonable basis for our opinion.

Critical Audit Matters

The critical audit matters communicated below

are matters arising from the current period audit of the financial statements that were communicated or required to be communicated to

the audit committee and that: (1) relate to accounts or disclosures that are material to the financial statements and (2) involved our

especially challenging, subjective, or complex judgments. The communication of critical audit matters does not alter in any way our opinion

on the financial statements, taken as a whole, and we are not, by communicating the critical audit matters below, providing separate opinions

on the critical audit matters or on the accounts or disclosures to which they relate.

Revenue Recognition from Contracts with Customers - Measurement

of the Transaction Price, including the Constraint on Variable Consideration for Rebates And Discounts

Critical Audit Matter Description

As discussed in Note 3 to the consolidated financial

statements, the Company offers sales incentives and other programs that they may make available to certain customers, which are considered

to be a form of variable consideration. The Company maintains estimated accruals and allowances using the expected value method. Revenue

recognized varies depending on whether a patient is covered by insurance or is not covered by insurance. In addition, the Company may

incur a revenue deductions related to the use of the Company’s rebate program.

The principal considerations for our determination

that performing procedures relating to the identification of contractual terms in customer arrangements to determine the transaction price

is a critical audit matter are there was significant judgment by management in identifying contractual terms due to the volume and customized

nature of the Company’s customer arrangements. This in turn led to significant effort in performing our audit procedures which were

designed to evaluate whether the contractual terms used in the determination of the transaction price and the timing of revenue recognition

were appropriately identified and determined by management and to evaluate the reasonableness of management’s estimates.

Addressing the matter involved performing procedures

and evaluating audit evidence in connection with forming our overall opinion on the consolidated financial statements.

How We Addressed the Matter in Our Audit

Our audit procedures included, amongst others:

/s/ Marcum llp

Marcum llp

We are uncertain as to the year we began serving

consecutively as the auditor of the Company’s financial statements; however, we are aware that we have been the Company’s

auditor consecutively since at least 2006.

New York, NY

July 14, 2021

SONOMA PHARMACEUTICALS, INC. AND SUBSIDIARIES

Consolidated Balance Sheets

(In thousands, except share amounts)

ASSETS

Current assets:

Cash and cash equivalents $ 7,396 $ 4,220

Prepaid expenses and other current assets 3,746 3,218

Current portion of deferred consideration, net of discount 218 209

Property and equipment, net 320 360

Operating lease, right of use assets 559 769

Deferred tax asset 829 –

Deferred consideration, net of discount, less current portion 630 763

LIABILITIES AND STOCKHOLDERS’ EQUITY

Current liabilities:

Accrued expenses and other current liabilities 1,843 1,154

Deferred revenue Invekra 54 52

Current portion of debt-PPP 120 -

Operating lease liabilities 250 240

Long-term deferred revenue Invekra 182 229

Long-term debt, less current portion – PPP – 1,310

Operating lease liabilities, less current portion 309 529

Commitments and Contingencies (Note 12)

Stockholders’ Equity

Accumulated other comprehensive loss (4,312 ) (4,579)

Total liabilities and stockholders’ equity $ 18,845 $ 14,987

The accompanying footnotes are an integral part

of these consolidated financial statements.

SONOMA PHARMACEUTICALS, INC., AND SUBSIDIARIES

Consolidated Statements of Comprehensive Income

(Loss)

(In thousands, except per share amounts)

Year ended March 31,

Operating expenses

Research and development 125 555

Selling, general and administrative 9,755 9,453

Interest income (expense), net (10 ) 4

Forgiveness of PPP Loan 723 –

Other expense, net (394 ) (594 )

Loss from continuing operations before income taxes (5,418 ) (3,902 )

Income tax benefit (expense) 332 (713 )

Loss from continuing operations, net of tax (5,086 ) (4,615 )

Income from discontinued operations, net of tax – 665

Loss per share: basic and diluted

Continuing operations $ (1.92 ) $ (2.31 )

Discontinued operations – 0.33

Total loss per share $ (1.92 ) $ (1.97 )

Weighted-average shares outstanding: basic and diluted 2,653 1,996

Other comprehensive loss

Foreign currency translation adjustments 267 1,031

The accompanying footnotes are an integral part

of these consolidated financial statements.

SONOMA PHARMACEUTICALS, INC., AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CHANGES IN STOCKHOLDERS’

EQUITY

For the Years Ended March 31, 2022 and 2021

(In thousands, except share amounts)

Shares Amount Shares Amount Capital Deficit Loss Total

Employee stock-based compensation expense – – – – 372 – – 372

Foreign currency translation adjustment – – – – – 267 267

Shares Amount Shares Amount Capital Deficit Loss Total

Shares issued in connection with vesting of restricted stock – – 3,919 – – – – –

Shares issued with conversion of C shares (1.55 ) – 17,222 – – – – –

Employee stock-based compensation expense – – – – 332 – – 332

Foreign currency translation adjustment – – – – – 1,031 1,031

The accompanying footnotes are an integral part

of these consolidated financial statements.

SONOMA PHARMACEUTICALS, INC., AND SUBSIDIARIES

CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands)

Year Ended March 31,

Cash flows from operating activities

Adjustments to reconcile net loss to net cash used in operating activities:

Depreciation and amortization 186 227

Recovery of doubtful accounts (125 ) (903 )

Stock-based compensation 382 371

Forgiveness of PPP loan (723 ) –

Deferred income tax expense (829 ) –

Operating lease right-of-use asset 223 –

Gain on sale of assets – (770 )

Changes in operating assets and liabilities:

Prepaid expenses and other current assets (460 ) (5 )

Deferred consideration, net of discount 160 143

Accrued expenses and other current liabilities 679 (668 )

Withholding tax payable 360 397

Operating lease liabilities (222 ) (215 )

Deferred revenue 900 (15 )

Net cash used in operating activities (4,248 ) (3,378 )

Cash flows from investing activities:

Purchases of property and equipment (137 ) (179 )

Proceeds from Micromed Transaction – 610

Net cash (used in) provided by investing activities (99 ) 388

Cash flows from financing activities:

Proceeds from issuance of common stock, net of issuance costs 7,554 –

Payments on PPP Loan (467 ) –

Proceeds from PPP Loan – 1,310

Proceeds from exercise of common stock options and purchase warrants 216 2,287

Principal payments on short-term debt (30 ) (481 )

Proceeds on short-term debt 123 –

Benefit from lease assumed less principal payments on ROU Assets – 192

Net cash provided by financing activities 7,396 3,308

Effect of exchange rate on cash and cash equivalents 127 211

Net increase in cash and cash equivalents 3,176 529

Cash and cash equivalents, beginning of year 4,220 3,691

Cash and cash equivalents, end of year $ 7,396 $ 4,220

Supplemental disclosure of cash flow information:

Cash paid for interest $ 24 $ 12

Cash paid for taxes $ 767 $ 941

Non-cash operating and financing activities:

Insurance premiums financed $ 748 $ 596

The accompanying footnotes are an integral part

of these consolidated financial statements.

SONOMA PHARMACEUTICALS, INC. AND SUBSIDIARIES

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

NOTE 1 – Organization and Recent

Developments

Organization

Sonoma Pharmaceuticals, Inc. (the “Company”)

was incorporated under the laws of the State of California in April 1999 and was reincorporated under the laws of the State of Delaware

in December 2006. The Company’s principal office was moved to Woodstock, Georgia from Petaluma, California in June 2020. The Company

is a global healthcare leader for developing and producing stabilized hypochlorous acid (“HOCl”) products for a wide range

of applications, including wound care, animal health care, eye care, oral care and dermatological conditions. The Company’s products

reduce infections, itch, pain, scarring and harmful inflammatory responses in a safe and effective manner. In-vitro and clinical studies

of HOCl show it to have impressive antipruritic, antimicrobial, antiviral and anti-inflammatory properties. The Company’s stabilized

HOCl immediately relieves itch and pain, kills pathogens and breaks down biofilm, does not sting or irritate skin and oxygenates the cells

in the area treated assisting the body in its natural healing process. The Company sells its products either directly or via partners

in 54 countries worldwide.

NOTE 2 – Liquidity and Financial

Condition

The Company reported a net loss of $5,086,000

for the year ended March 31, 2022. At March 31, 2022 and 2021, the Company’s accumulated deficit amounted to $184,363,000

and $179,277,000, respectively. The Company had working capital of $10,611,000 and $8,905,000 as of March 31, 2022 and 2021,

respectively.

Management believes that the Company has access

to additional capital resources through possible public or private equity offerings, debt financings, corporate collaborations or other

means; however, the Company cannot provide any assurance that other new financings will be available on commercially acceptable terms,

if needed. If the economic climate in the U.S. deteriorates, the Company’s ability to raise additional capital could be negatively

impacted. If the Company is unable to secure additional capital, it may be required to take additional measures to reduce costs in order

to conserve its cash in amounts sufficient to sustain operations and meet its obligations. These measures could cause significant delays

in the Company’s continued efforts to commercialize its products, which is critical to the realization of its business plan and

the future operations of the Company. These matters raise substantial doubt about the Company’s ability to continue as a going concern.

The accompanying consolidated financial statements do not include any adjustments that may be necessary should the Company be unable to

continue as a going concern.

COVID – 19

On March 11, 2020 the

World Health Organization declared the novel strain of coronavirus (“COVID-19”) a global pandemic and recommended containment

and mitigation measures worldwide. In an effort to mitigate the continued spread of the virus, federal, state and local governments, as

well as certain private entities have mandated various restrictions, including travel restrictions, restrictions on public gatherings

and quarantining of people who may have been exposed to the virus. As a result of these restrictions, together with a general fear of

the impact on the global economy and financial markets, there is significant uncertainty surrounding the potential impact on the Company.

As events are rapidly changing, the Company is unable to accurately predict the impact that COVID-19 will have on its business due to

uncertainties including, but not limited to, the duration of quarantines and other travel restrictions within China, the U.S. and other

affected countries, the ultimate geographical spread of the virus, the severity of the disease, the duration of the outbreak and the public’s

response to the outbreak.

NOTE 3 – Summary of Significant Accounting Policies

Principles of Consolidation

The accompanying consolidated financial statements

include the accounts of the Company and its wholly-owned subsidiaries, Aquamed Technologies, Inc. (“Aquamed”), Oculus Technologies

of Mexico S.A. de C.V. (“OTM”), and Sonoma Pharmaceuticals Netherlands, B.V. (“SP Europe”). Aquamed has no current

operations. All significant intercompany accounts and transactions have been eliminated in consolidation. The functional currency for

the Company's wholly-owned subsidiaries incorporated outside the United States (“U.S.”) is denominated in local currency.

All intercompany transactions and balances have been eliminated in consolidation.

Basis of presentation

The accompanying consolidated

financial statements have been prepared by the Company pursuant to the rules and regulations of the U.S. Securities and Exchange Commission

("SEC") and are in conformity with U.S. generally accepted accounting principles ("GAAP"). The Company’s fiscal

year end is March 31. Unless otherwise stated, all years and dates refer to the fiscal year.

Cash and Cash Equivalents

Cash and cash equivalents

include cash on hand and all highly liquid investments with an original maturity of three months or less when purchased. The Company’s

cash equivalents are held in prime money market investments with strong sponsor organizations which are monitored on a continuous basis.

Use of Estimates

The preparation of consolidated financial statements

in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities

and disclosures of contingent liabilities at the dates of the consolidated financial statements and the reported amounts of revenues and

expenses during the reporting periods. Actual results could differ from these estimates. Significant estimates and assumptions include

reserves and write-downs related to receivables and inventories, the recoverability of long-lived assets, the valuation allowance relating

to the Company’s deferred tax assets, valuation of equity, fair value allocation of assets sold to Invekra, and the estimated amortization

periods of upfront product licensing fees received from customers. Periodically, the Company evaluates and adjusts estimates accordingly.

Revenue Recognition

On April 1, 2018, the Company adopted Accounting

Standards Update ("ASU"), "Revenue from Contracts with Customers Topic 606” (“Topic 606”) using the modified

retrospective method. There was no material impact to the Company upon the adoption of Topic 606. Revenue is recognized when the Company

transfers promised goods or services to the customer, in an amount that reflects the consideration which the Company expects to receive

in exchange for those goods or services. In determining the appropriate amount of revenue to be recognized as the Company fulfills its

obligations under the agreement, the Company performs the following steps: (i) identification of the promised goods or services in

the contract; (ii) determination of whether the promised goods or services are performance obligations, including whether they are

distinct in the context of the contract; (iii) measurement of the transaction price, including the constraint on variable consideration;

(iv) allocation of the transaction price to the performance obligations; and (v) recognition of revenue when (or as) the Company

satisfies each performance obligation. The Company only applies the five-step model to contracts when it is probable that it will collect

the consideration it is entitled to in exchange for the goods or services it transfers to the customer.

The Company derives the majority of its revenue

through sales of its products directly to end users and to distributors. The Company also sells products to a customer base, including

hospitals, medical centers, doctors, pharmacies, distributors and wholesalers. The Company also has entered into agreements to license

its technology and products.

The Company considers customer purchase orders,

which in some cases are governed by master sales agreements, to be the contracts with a customer. For each contract, the Company considers

the promise to transfer products, each of which are distinct, to be the identified performance obligations. In determining the transaction

price the Company evaluates whether the price is subject to refund or adjustment to determine the net consideration to which it expects

to be entitled.

For all of its sales to non-consignment distribution

channels, revenue is recognized when control of the product is transferred to the customer (i.e. when its performance obligation is satisfied),

which typically occurs when title passes to the customer upon shipment but could occur when the customer receives the product based on

the terms of the agreement with the customer. For product sales to its value-added resellers, non-stocking distributors and end-user customers,

the Company grants return privileges to its customers, and because the Company has a long history with its customers, the Company is able

to estimate the amount of product that will be returned. Sales incentives and other programs that the Company may make available

to these customers are considered to be a form of variable consideration, and the Company maintains estimated accruals and allowances

using the expected value method.

The Company has entered into consignment arrangements,

in which goods are left in the possession of another party to sell. As products are sold from the customer to third parties, the Company

recognizes revenue based on a variable percentage of a fixed price. Revenue recognized varies depending on whether a patient is

covered by insurance or is not covered by insurance. In addition, the Company may incur a revenue deduction related to the use of the

Company’s rebate program.

Sales to stocking distributors are made under

terms with fixed pricing and limited rights of return (known as “stock rotation”) of the Company’s products held in

their inventory. Revenue from sales to distributors is recognized upon the transfer of control to the distributor.

The Company assessed the promised goods and services

in the technical support to Invekra for a ten-year period as being a distinct service that Invekra can benefit from on its own and is

separately identifiable from any other promises within the contract. Given that the distinct service is not substantially the same as

other goods and services within the Invekra contract, the Company accounted for the distinct service as a performance obligation.

Service revenue from testing contracts is recognized

as tests are completed and a final report is sent to the customer.

Concentration of Credit Risk and Major Customers

Financial instruments that potentially subject

the Company to concentration of credit risk consist principally of cash, cash equivalents and accounts receivable. Cash and cash equivalents

are maintained in financial institutions in the United States, Mexico and the Netherlands. The Company is exposed to credit risk in the

event of default by these financial institutions for amounts in excess of the Federal Deposit Insurance Corporation insured limits. Cash

and cash equivalents held in foreign banks are intentionally kept at minimal levels, and therefore have minimal credit risk associated

with them.

The Company grants credit to its business customers,

which are primarily located in Mexico, Europe and the United States. Collateral is generally not required for trade receivables. The Company

maintains allowances for potential credit losses. At March 31, 2022, one customer represented 20% of our net accounts

receivable balance, one customer represented 15% of our net accounts receivable balance, and one customer represented

14% of our net accounts receivable balance. At March 31, 2021, one customer represented 17% of our net accounts receivable balance, one customer represented 16%

of our net accounts receivable balance, and one customer represented 14% of our net accounts receivable balance. For the year ended March 31, 2022, one customer represented 10%, one customer represented 17%, and one customer represented

21% of net revenues. For the year ended March 31, 2021, one customer represented 32%, and one customer represented 15% of net revenues.

Accounts Receivable

Trade accounts receivable are recorded net of

allowances for cash discounts for prompt payment, doubtful accounts, and sales returns. Estimates for cash discounts and sales returns

are based on analysis of contractual terms and historical trends.

The Company’s policy is to reserve for uncollectible

accounts based on its best estimate of the amount of probable credit losses in its existing accounts receivable. The Company periodically

reviews its accounts receivable to determine whether an allowance for doubtful accounts is necessary based on an analysis of past due

accounts and other factors that may indicate that the realization of an account may be in doubt. Other factors that the Company considers

include its existing contractual obligations, historical payment patterns of its customers and individual customer circumstances, an analysis

of days sales outstanding by customer and geographic region, and a review of the local economic environment and its potential impact on

government funding and reimbursement practices. Account balances deemed to be uncollectible are charged to the allowance after all means

of collection have been exhausted and the potential for recovery is considered remote. The allowance for doubtful accounts represents

probable credit losses at March 31, 2022 and 2021 in the amounts of $0 and $125,000, respectively. Additionally, at March 31, 2022 and

2021, the Company has allowances of $81,000 and $1,488,000, respectively, related to potential discounts, returns, distributor fees and

rebates. The allowances are included in Accounts Receivable, net in the accompanying consolidated balance sheets.

Inventories

Inventories are stated at the lower of cost, cost

being determined on a standard cost basis (which approximates actual cost on a first-in, first-out basis), or net realizable value.

Due to changing market conditions, estimated future

Source: SEC EDGAR (public domain) · 10-K for the period ended 2022-03-31, filed 2022-07-13 · accession 0001683168-22-004940

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