Home / drug / D-0167-2026 Class II Reported 2025-11-26
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. Recalled by DermaRite Industries, LLC
Reason for Recall CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Recall Number D-0167-2026
Classification Class II
Status Ongoing
Category drug
Initiated 2025-08-27
Reported 2025-11-26
Distribution Nationwide in the USA
Code Info All lots on or before expiry date 08/2027 Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer .