Dr. Luke FUNGAL NAIL RENEWAL
- Product NDC
- 87147-005
- 11-digit product format
- 871470005
- Labeler code
- 87147
- Product ID
- 87147-005_43427b44-bdaa-bc1a-e063-6294a90aaed6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FUNGAL NAIL RENEWAL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- DANOUS LAND FLOOW LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-10-13
- Substance
- TOLNAFTATE
- Active strength
- 1 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr. Luke FUNGAL NAIL RENEWAL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313423 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87147-005-01 | Dr. Luke FUNGAL NAIL RENEWAL | 30 mL in 1 BOTTLE | LIQUID | 30 | | 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 |
|---|
| 87147-005-01 | 87147000501 | 30 mL in 1 BOTTLE (87147-005-01) | 30 ml | 2018-10-13 | No | No | Current |