Toenail Fungus Treatment
- Product NDC
- 87413-002
- 11-digit product format
- 874130002
- Labeler code
- 87413
- Product ID
- 87413-002_4dc1d7f7-e4af-c54b-e063-6394a90aa420
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Terbinafine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shenzhen Wankelai E-commerce Co., Ltd.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-24
- Substance
- TERBINAFINE
- Active strength
- .01 g/mL
- Pharmacologic classes
- Allylamine Antifungal [EPC], Allylamine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Toenail Fungus Treatment
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TERBINAFINE | .01 g/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G7RIW8S0XP |
| Rxcui | 992531 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87413-002-01 | Toenail Fungus Treatment | 10 mL in 1 BOTTLE | LIQUID | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87413-002-01 | 87413000201 | 10 mL in 1 BOTTLE (87413-002-01) | 10 ml | 2026-03-24 | No | No | Current |