Drug Recall: Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West S
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.
Product Description
Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
Distribution
Nationwide in the USA
States Affected
NATIONWIDE
Quantity Affected
8,378 containers
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0169-2026
Status: ongoing
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