Antifungal Liquid
- Product NDC
- 56104-902
- 11-digit product format
- 561040902
- Labeler code
- 56104
- Product ID
- 56104-902_3bb9fc56-4b58-0d7e-e063-6394a90a56cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-11-06
- Marketing end
- 2026-11-30
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antifungal Liquid
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 10 mg/mL |
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 |
|---|
| 56104-902-01 | Antifungal Liquid | 1 in 1 CARTON | LIQUID | 1 | | 2 |
| 56104-902-01 | Antifungal Liquid | 30 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56104-902 | ANTIFUNGAL LIQUID (TOLNAFTATE) LIQUID [PREMIER BRANDS OF AMERICA INC] | 1 | Current NDC, 2 package rows | 20241108_2644ba07-aaee-6402-e063-6394a90a2827.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56104-902-01 | 56104090201 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-902-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR | 2024-11-06 | 2026-11-30 | No | No | Historical |