Class II

Drug Recall: DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08

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.

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

2,389 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0165-2026

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.

DermaRite Industries, LLC Drug Recall: DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08 | SafeCheck