DermaRite Industries, LLC recalls DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side
Recalled November 26, 2025 · FDA recall D-0165-2026 · DermaRite Industries
Hazard
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. · FDA Class II
Units
2,389 bottles
Sold at
Nationwide in the USA
Description
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Product
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
Manufacturer(s)
DermaRite Industries, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →