PlainRecalls
FDA Drug Moderate Class II Ongoing

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.

Reported: November 26, 2025 Initiated: August 27, 2025 #D-0167-2026

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.

Reason for Recall

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

Details

Recalling Firm
DermaRite Industries, LLC
Units Affected
576 containers
Distribution
Nationwide in the USA
Location
North Bergen, NJ

Frequently Asked Questions

What product was recalled?
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. Units affected: 576 containers.
Why was this product recalled?
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 26, 2025. Severity: Moderate. Recall number: D-0167-2026.