DermaRite Industries, LLC recalls 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-

Recalled November 26, 2025 · FDA recall D-0169-2026 · DermaRite Industries

Hazard

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

Units

8,378 containers

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

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.

Manufacturer(s)

DermaRite Industries, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →