Tolnaftate Antifungal Powder
- Product NDC
- 73469-0619
- 11-digit product format
- 734690619
- Labeler code
- 73469
- Product ID
- 73469-0619_fee7a27d-f2f9-4d6f-920e-7ba0d39a4bea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- SCHOLL'S WELLNESS COMPANY LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-26
- 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 Powder
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73469-0619-4 | Tolnaftate Antifungal Powder | 113 g in 1 BOTTLE | POWDER | 113 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73469-0619-4 | 73469061904 | 113 g in 1 BOTTLE (73469-0619-4) | 113 g | 2025-11-26 | No | No | Historical |