Class II

Drug Recall: 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 070

DermaRite Industries, LLC · August 27, 2025

Reason for Recall

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

Product Description

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.

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

576 containers

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0167-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.