Quick answers
- What is Lotrimin?
- Lotrimin is a brand name of Miconazole, Butenafine, Clotrimazole and Tolnaftate, an over-the-counter medicine. The FDA NDC Directory lists 15 Lotrimin products in 6 strengths and forms.
- Who makes Lotrimin?
- Bayer HealthCare LLC. holds the FDA application for Lotrimin (NDA021307, approved December 7, 2001).
- Is there a generic or store brand of Lotrimin?
- Yes. The FDA NDC Directory lists 198 other products with the same active ingredients, strength and form as a Lotrimin product, 198 of them generic or store brands. Ask your pharmacist whether one is right for you.
- Has Lotrimin been recalled?
- FDA enforcement reports list 4 recalls of Lotrimin products; the newest started October 1, 2021. A recall usually concerns specific lots, not every product.
What Lotrimin is
Each Lotrimin product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Miconazole · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| miconazole nitrate 2% aerosol, powder (topical) | Lotrimin AF Jock Itch, Lotrimin AF, Lotrimin AF Deodorant | 5 products, 4 companies | DailyMed |
| miconazole nitrate 2% powder (topical) | Lotrimin AF Jock Itch, Lotrimin Antifungal | 32 products, 26 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Miconazole →
Butenafine · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| butenafine hydrochloride 1% cream (topical) | Lotrimin Ultra Ringworm, Lotrimin Ultra, Lotrimin Ultra Athletes Foot, Lotrimin Ultra Jock Itch | 17 products, 13 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Butenafine →
Clotrimazole · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| clotrimazole 1% cream (topical) | Lotrimin, Lotrimin Antifungal | 133 products, 81 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Clotrimazole →
Tolnaftate · over-the-counter medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| tolnaftate 1% aerosol, powder (topical) | Lotrimin Daily Prevention Deo, Lotrimin Daily Prevent Deodorant | 7 products, 4 companies | DailyMed |
| tolnaftate 1% powder (topical) | Lotrimin Daily Prevention | 4 products, 4 companies | DailyMed |
Its page quotes the Drug Facts label and lists every brand and store brand: Tolnaftate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021307 | Bayer Healthcare LLC | December 7, 2001 | 4 |
Companies that list Lotrimin
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Lotrimin products.
- Bayer Healthcare LLC.15 products
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
October 1, 2021 · Class II · Terminated · D-0239-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
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. — Bayer Healthcare Pharmaceuticals Inc.
-
October 1, 2021 · Class II · Terminated · D-0254-2022
cGMP Deviations: LOTRIMIN AF (Tolnaftate 1%) manufactured at the same facility where other lots were found to be contaminated with benzene.
LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, UPC 0 41100 58720 6, NDC 11523-0010-2; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, Packaged with L — Bayer Healthcare Pharmaceuticals Inc.
-
October 1, 2021 · Class II · Terminated · D-0240-2022
cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
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 Healthcar — Bayer Healthcare Pharmaceuticals Inc.
-
October 1, 2021 · Class I · Terminated · D-0249-2022
Chemical Contamination: presence of benzene
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. — Bayer Healthcare Pharmaceuticals Inc.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.