Antifungal Liquid
- Product NDC
- 82442-998
- 11-digit product format
- 824420998
- Labeler code
- 82442
- Product ID
- 82442-998_3c6dd780-6ac8-d88d-e063-6394a90a1124
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-12
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 82442-998_3c6dd780-6ac8-d88d-e063-6394a90a1124
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- Antifungal Liquid
- Generic name
- Tolnaftate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Marketing start
- 2025-08-12
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M005
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| TOLNAFTATE | 10 mg/mL |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313423 |
| Spl Set Id | 3c6dd772-0d26-b659-e063-6294a90a5bf8 |
| Manufacturer Name | Target Corporation |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 06KB629TKV | TOLNAFTATE | 2398-96-1 | TOLNAFTATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-998-01 | 82442099801 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (82442-998-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR | 2025-08-12 | No | No | Current |