Tolnaftate
- Product NDC
- 36800-006
- 11-digit product format
- 368000006
- Labeler code
- 36800
- Product ID
- 36800-006_42f46f47-3bb1-8942-e063-6294a90aef7d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antifungal Liquid Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Topco Associates LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-01-03
- Substance
- TOLNAFTATE
- Active strength
- 1.5 g/150g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolnaftate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1.5 g/150g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313421 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-006-53 | Tolnaftate | 150 g in 1 CAN | AEROSOL, SPRAY | 150 | | 10 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-006 | TOLNAFTATE (ANTIFUNGAL LIQUID SPRAY) AEROSOL, SPRAY [TOPCO ASSOCIATES LLC] | 9 | Current NDC, Legacy NDC, 1 package rows | 20241213_3dd0df06-3c74-4c34-a69e-4240945f5fa5.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 |
|---|
| 36800-006-53 | 36800000653 | 150 g in 1 CAN (36800-006-53) | 150 g | 2012-01-03 | 0000-00-00 | No | No | Current |