Tolnaftate
- Product NDC
- 41250-635
- 11-digit product format
- 412500635
- Labeler code
- 41250
- Product ID
- 41250-635_48d4b9e3-cfe5-d3af-e063-6294a90aedeb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Foot Odor Control Powder Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-01-05
- Marketing end
- 2026-12-31
- Substance
- TOLNAFTATE
- Active strength
- 1.3 g/113g
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolnaftate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1.3 g/113g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-635-40 | Tolnaftate | 113 g in 1 CAN | AEROSOL, SPRAY | 113 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-635 | TOLNAFTATE (FOOT ODOR CONTROL POWDER SPRAY) AEROSOL, SPRAY [MEIJER DISTRIBUTION INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241016_b3ba676e-9377-4665-b99e-d4143df96b36.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-635-40 | 41250063540 | 113 g in 1 CAN (41250-635-40) | 113 g | 2012-01-05 | 2026-12-31 | No | No | Current |