Antifungal Foot Treatment
- Product NDC
- 83004-016
- 11-digit product format
- 830040016
- Labeler code
- 83004
- Product ID
- 83004-016_2fae9415-875b-58bc-e063-6394a90a3612
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Butenafine Hydrochloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Rida LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-02-27
- Substance
- BUTENAFINE HYDROCHLORIDE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Benzylamine Antifungal [EPC], Benzylamines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83004-016 | ANTIFUNGAL FOOT TREATMENT (BUTENAFINE HYDROCHLORIDE) GEL [RIDA LLC] | 1 | Current NDC | 20250309_3a735ca5-4717-43a1-ab42-76f310bcfe00.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83004-016-01 | 83004001601 | 1 TUBE in 1 CARTON (83004-016-01) / 20 g in 1 TUBE | 1 tube | 2025-02-27 | No | No | Historical |