Topical Hydrogen Peroxide Solution Recalled for Incorrect Back Label
Consumer Product Partners is recalling Hydrogen Peroxide Topical Solution bottles with incorrect back labels indicating 91% Isopropyl Alcohol. The labeling mixup affects 25,932 bottles distributed in Virginia.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II labeling error with no reported illnesses, injuries, or deaths. The hazard is confusion about product identity due to incorrect label information rather than documented adverse events. Per FDA rubric criteria, labeling errors without reported harm warrant a Moderate severity score.
Plain-English summary
Consumer Product Partners, LLC is recalling certain bottles of Hydrogen Peroxide Topical Solution, USP (NDC 0869-0871-45) due to a labeling mixup. Approximately 25,932 bottles in lot 0643188 (expiration date 10/22/2026) were distributed with an incorrect back label that indicates 91% Isopropyl Alcohol instead of the correct hydrogen peroxide labeling.
The incorrect back label creates confusion about the product's actual identity and contents. This labeling error could lead consumers to misidentify or potentially misuse the product based on false label information.
The affected bottles were distributed in Virginia. Consumers who have purchased this product should check the lot number and expiration date on the bottle. If the product matches the recall information, discontinue use and follow instructions from the recalling firm or the FDA regarding return or disposal.
This is a Class II recall issued by the Food and Drug Administration.
The recalled product
- Product
- HYDROGEN PEROXIDE (HYDROGEN PEROXIDE)
- Brand
- HYDROGEN PEROXIDE
- Manufacturer
- Consumer Product Partners, LLC
- Category
- Drug — Topical OTC
- Affected units
- 25,932
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot 0643188
- exp. date 10/22/2026
Distribution
Distributed in 1 state:
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