Tolnaftate
- Product NDC
- 30142-841
- 11-digit product format
- 301420841
- Labeler code
- 30142
- Product ID
- 30142-841_426569c9-2a19-67ec-e063-6294a90a6941
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate Powder Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Kroger Co.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-03-11
- Substance
- TOLNAFTATE
- Active strength
- 1.3 g/130g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolnaftate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1.3 g/130g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 705934 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 30142-841-01 | Tolnaftate | 130 g in 1 CAN | AEROSOL, SPRAY | 130 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30142-841 | TOLNAFTATE (TOLNAFTATE POWDER SPRAY) AEROSOL, SPRAY [KROGER CO.] | 3 | Current NDC, 1 package rows | 20241213_f5c8dccd-8e69-6a01-e053-2a95a90a6972.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 |
|---|
| 30142-841-01 | 30142084101 | 130 g in 1 CAN (30142-841-01) | 130 g | 2022-03-11 | No | No | Current |