TOLNAFTATE ANTIFUNGAL
- Product NDC
- 71335-2249
- 11-digit product format
- 713352249
- Labeler code
- 71335
- Product ID
- 71335-2249_338b2c92-5505-4320-81d5-b5d3548f27e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOLNAFTATE
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-08-01
- Substance
- TOLNAFTATE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 06KB629TKV | TOLNAFTATE | 2398-96-1 | TOLNAFTATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2249-1 | 71335224901 | 45 g in 1 BOTTLE, DISPENSING (71335-2249-1) | 45 g | 2024-01-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| GC TOLNAFTATE | Bryant Ranch Prepack | 2024-01-29 | HUMAN OTC DRUG LABEL | 100 |