FDA-Drug2025-11-26Class II
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.
DermaRite Industries, LLC
Hazard
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Sold states
Nationwide in the USA
Affected count
8,378 containers
Manufactured in
7777 W Side Ave, North Bergen, NJ, United States
Products
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0169-2026Don't want to check this manually?
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