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Class II · ModerateActive recall

Hydrogen Peroxide

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot 0643188, exp. date 10/22/2026
Where it was soldVA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byVi-Jon, LLC
Brand nameHYDROGEN PEROXIDE
Generic nameHYDROGEN PEROXIDE
Active ingredient(s)HYDROGEN PEROXIDE
Distributed by / forConsumer Product Partners, LLC
NDC0869-0871-45
Show the full FDA record
Full product label[CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ (1 QT) 946 mL per bottle, NDC 0869-0871-45; [INCORRECT BACK LABEL] Isopropyl alcohol 91%, Dist. by: Amazon.com Services, LLC, Seattle, WA 98109.
Recalling firmConsumer Product Partners, LLC
DistributionVA
Quantity25,932 bottles
Recall initiated2025-03-07
Report date2025-04-02
Recall completed—
Recall numberD-0302-2025
ClassificationClass II
FDA statusOngoing
Origin on fileSmyrna TN United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.