FDAOctober 1, 2021drug

LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 59036 7, NDC 11523-0010-1.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.

What to do

FDA enforcement status: Terminated

Brands named

bayer healthcare pharmaceuticalsbayerbayer healthcare

UPCs

041100590367

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 59036 7, NDC 11523-0010-1. — Recall Details · AllClear