CLASS II ONGOING Drug recall · Reported 2 Apr 2025 · FDA Enforcement Report
[Correct Front Panel] Hydrogen Peroxide Topical Solution recalled
Consumer Product Partners is recalling [Correct Front Panel] Hydrogen Peroxide Topical Solution, USP per, distributed in Virginia. The recall was initiated on 7 Mar 2025 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0302-2025
- FDA event ID
- 96475
- Recalling firm
- Consumer Product Partners, Smyrna, TN
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 7 Mar 2025
- FDA classified
- 27 Mar 2025
- Reported
- 2 Apr 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Packaging Defects
- Drug class
- Creams, Ointments & Gels
Timeline
| 7 Mar 2025 | Recall initiated by company | |
| 27 Mar 2025 | Classified by FDA | +20 days |
| 2 Apr 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
[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.
Where it was distributed
VA
Stores named: Amazon, Online Retailers
Questions about this recall
Why was it recalled?
Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
Which lots are affected?
Lot 0643188, exp. date 10/22/2026
Where was it sold?
VA
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 2 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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|---|---|---|---|---|---|
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