Dermatool Fungal Nail Treatment
- Product NDC
- 72839-510
- 11-digit product format
- 728390510
- Labeler code
- 72839
- Product ID
- 72839-510_29a5e538-8ed7-677a-e063-6394a90a4cd6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate 1%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Derma Care Research Labs, LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-04-06
- 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
- Dermatool Fungal Nail Treatment
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72839-510-01 | Dermatool Fungal Nail Treatment | 1 in 1 CARTON | LIQUID | 1 | | 2 |
| 72839-510-01 | Dermatool Fungal Nail Treatment | 15 mL in 1 BOTTLE, GLASS | LIQUID | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72839-510 | DERMATOOL FUNGAL NAIL TREATMENT (TOLNAFTATE 1%) LIQUID [DERMA CARE RESEARCH LABS, LLC] | 2 | Current NDC, 2 package rows | 20241222_fbc1a55e-b994-4962-e053-6394a90a13ba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72839-510-01 | 72839051001 | 1 BOTTLE, GLASS in 1 CARTON (72839-510-01) / 15 mL in 1 BOTTLE, GLASS | 2023-04-06 | No | No | Historical |