Recalls / Brands / Lotrimin Daily Prevention Deo
Lotrimin Daily Prevention Deo
4 FDA drug recalls involving brand “Lotrimin Daily Prevention Deo” — 1 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2021-10-01 | Class II | LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer H | Bayer Healthcare Pharmaceuticals Inc. |
| 2021-10-01 | Class II | LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, UPC 0 41100 587 | Bayer Healthcare Pharmaceuticals Inc. |
| 2021-10-01 | Class II | LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) | Bayer Healthcare Pharmaceuticals Inc. |
| 2021-10-01 | Class I | Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray, NET WT 160g (5.6 OZ) can, Dist by: Bayer | Bayer Healthcare Pharmaceuticals Inc. |