Tolnaftate
- Product NDC
- 37808-514
- 11-digit product format
- 378080514
- Labeler code
- 37808
- Product ID
- 37808-514_42b86eda-83cf-5418-e063-6294a90ae383
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Foot Odor Control Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- HEB
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-01-05
- Substance
- TOLNAFTATE
- Active strength
- 1.13 g/113g
- 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 | 1.13 g/113g |
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 |
|---|
| 37808-514-40 | 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 |
|---|
| 37808-514 | TOLNAFTATE (FOOT ODOR CONTROL SPRAY) AEROSOL, SPRAY [HEB] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241213_c585605b-ecb8-4dd8-9205-a9be02d751fa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-514-40 | 37808051440 | 113 g in 1 CAN (37808-514-40) | 113 g | 2012-01-05 | 0000-00-00 | No | No | Current |