DermaRite Industries, LLC recalls Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per

Recalled November 26, 2025 · FDA recall D-0167-2026 · DermaRite Industries

Hazard

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

Units

576 containers

Sold at

Nationwide in the USA

Description

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

Product

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.

Manufacturer(s)

DermaRite Industries, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →