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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Hydrogen Peroxide Topical Solution Recalled for Incorrect Back Label

Agency Publication Date: March 27, 2025
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Summary

Consumer Product Partners, LLC is recalling 25,932 bottles of Hydrogen Peroxide Topical Solution, USP (32 FL OZ) because of a label mix-up. While the front label correctly identifies the product as hydrogen peroxide, the back label incorrectly identifies it as 91% Isopropyl Alcohol. This error means the bottle contains the wrong ingredient information and safety directions for the actual product inside.

Risk

Using the product based on the incorrect back label could lead to improper wound treatment or accidental misuse, as the instructions and warnings for isopropyl alcohol differ from those for hydrogen peroxide.

What You Should Do

  1. This recall affects 32 FL OZ (1 QT) bottles of Hydrogen Peroxide Topical Solution, USP, featuring NDC 0869-0871-45, lot number 0643188, and an expiration date of 10/22/2026.
  2. Check the back of the bottle to see if it incorrectly identifies the product as 'Isopropyl alcohol 91%' and lists Amazon.com Services, LLC as the distributor.
  3. If you have health concerns, contact your healthcare provider or pharmacist.
  4. Return any unused product to the place of purchase for a refund, throw it away, or contact Consumer Product Partners, LLC for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Hydrogen Peroxide Topical Solution, USP
Variants: 32 FL OZ (1 QT), 946 mL
Lot Numbers:
0643188 (Exp 10/22/2026)
NDC:
0869-0871-45

Bottles have correct front panel for Hydrogen Peroxide but incorrect back label for Isopropyl alcohol 91%.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96475
Status: Active
Manufacturer: Consumer Product Partners, LLC
Sold By: Amazon.com Services, LLC
Manufactured In: United States
Units Affected: 25,932 bottles
Distributed To: Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.