FDA recall record

HYDROGEN PEROXIDE [CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ recall — FDA D-0302-2025

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

Class IIclassification
D-0302-2025official record ID
Apr 2, 2025report date

Recall record at a glance

Official recordD-0302-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmConsumer Product Partners, LLC
Report dateApr 2, 2025
Recall initiation dateMar 7, 2025
Quantity25,932 bottles
LocationSmyrna, TN, United States

Official product description

[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.

Why the product was recalled

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

Distribution information

VA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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