Drug recall D-0249-2022
Product
Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 58720 6, NDC 11523-0010-2.
Reason for recall
Chemical Contamination: presence of benzene
Lots and codes
Lot # TN0023D, EXP 2/28/2022; TN004BX, EXP 6/30/2022;
Recall details
- Recalling firm
- Bayer Healthcare Pharmaceuticals Inc., Whippany, NJ
- Quantity
- 579,456 cans
- Distribution
- Distributed Nationwide in the US, Puerto Rico, Canada and Mexico through a variety of retail channels.
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 1, 2021
- Terminated
- June 26, 2023
Related products
- Lotrimin Daily Prevention Deo – drug information
- NDC 11523-0010 Lotrimin Daily Prevention Deo · Tolnaftate 10 mg/g · Bayer HealthCare LLC.