Tolnaftate
- Product NDC
- 82442-402
- 11-digit product format
- 824420402
- Labeler code
- 82442
- Product ID
- 82442-402_42f403bf-8d23-373c-e063-6394a90a203d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antifungal Powder Spray with Baking Soda
- Dosage form
- AEROSOL, POWDER
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-31
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/g
- 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 | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 705934 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82442-402-01 | Tolnaftate | 113 g in 1 CAN | AEROSOL, 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 |
|---|
| 82442-402-01 | 82442040201 | 113 g in 1 CAN (82442-402-01) | 113 g | 2025-06-02 | No | No | Current |