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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TOLNAFTATE ANTIFUNGAL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313422 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2249-1 | TOLNAFTATE ANTIFUNGAL | 45 g in 1 BOTTLE, DISPENSING | POWDER | 45 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2249 | TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) POWDER [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240130_fbbd159c-217e-46d3-963c-ba0bd1e9bbe8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |