United States · FDA National Drug Code directory
Lotrimin Ultra
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 11523-0082_4526ca36-993f-b574-e063-6294a90a8fba
- Product NDC
- 11523-0082
- Form
- CREAM
- Composition / generic term
- Butenafine hydrochloride
- Labeler
- Bayer Healthcare LLC.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20211220
- Source listing expiry
- 20261231
Source-listed ingredients
- BUTENAFINE HYDROCHLORIDE — 1 g/100g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE, WITH APPLICATOR in 1 CARTON (11523-0082-1) / 20 g in 1 TUBE, WITH APPLICATOR · 11523-0082-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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