FDAOctober 1, 2021drug

LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) single pack, UPC 0 41100 58720 6, NDC 11523-0010-2; (b) 3-pack, UPC 0 41100 58961 3; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland,

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

041100587206041100589613

Recall history

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

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