Tolnafate
- Product NDC
- 21130-215
- 11-digit product format
- 211300215
- Labeler code
- 21130
- Product ID
- 21130-215_41eeadfa-d4f5-edd1-e063-6394a90ae3e5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate Powder Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Better Living Brands LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-09-27
- Substance
- TOLNAFTATE
- Active strength
- 1.3 g/130g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolnafate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1.3 g/130g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 705934 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-215-00 | Tolnafate | 130 g in 1 CAN | AEROSOL, SPRAY | 130 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-215 | TOLNAFATE (TOLNAFTATE POWDER SPRAY) AEROSOL, SPRAY [BETTER LIVING BRANDS LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241109_ccff8d63-ee7d-eada-e053-2995a90ac5dd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-215-00 | 21130021500 | 130 g in 1 CAN (21130-215-00) | 130 g | 2021-09-27 | 0000-00-00 | No | No | Current |