FDAAugust 27, 2025drug

Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

What to do

FDA enforcement status: Ongoing

Brands named

dermarite

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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