NAIL FUNGUS TREATMENT
- Product NDC
- 85834-001
- 11-digit product format
- 858340001
- Labeler code
- 85834
- Product ID
- 85834-001_38c2639f-43dc-d05c-e063-6394a90a0bc8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate 1% NAIL FUNGUS TREATMENT
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shenzhen Bullfighting Trading Co., Ltd.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-30
- 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
- NAIL FUNGUS 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 |
|---|
| 85834-001-01 | NAIL FUNGUS TREATMENT | 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 |
|---|
| 85834-001-01 | 85834000101 | 30 mL in 1 BOTTLE (85834-001-01) | 30 ml | 2025-06-30 | No | No | Historical |