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.
| Source | FDA Drug Enforcement |
|---|---|
| Category | Drug |
| Severity | Medium |
| Status | ongoing |
| Recall date | August 27, 2025 |
| Reported | November 26, 2025 |
| Recalling firm | DermaRite Industries, LLC |
| Country / region | United States NJ |
Hazard
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Affected products
- 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, 777
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