ANTIFUNGAL FOOT
- Product NDC
- 52000-418
- 11-digit product format
- 520000418
- Labeler code
- 52000
- Product ID
- 52000-418_a19d28ce-56bb-4904-9949-0fc2ddb70f9d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Universal Distribution Center LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-07-16
- Substance
- TOLNAFTATE
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ANTIFUNGAL FOOT
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313421 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-418-03 | ANTIFUNGAL FOOT | 103 g in 1 CAN | AEROSOL, SPRAY | 103 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-418 | ANTIFUNGAL FOOT (TOLNAFTATE) AEROSOL, SPRAY [UNIVERSAL DISTRIBUTION CENTER LLC] | 1 | Current NDC, 1 package rows | 20240727_10579848-5793-4d72-ad5f-62d191c71074.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 52000-418-03 | 52000041803 | 103 g in 1 CAN (52000-418-03) | 103 g | 2024-07-16 | No | No | Current |