Menthol
- Product NDC
- 36800-252
- 11-digit product format
- 368000252
- Labeler code
- 36800
- Product ID
- 36800-252_42f4c54c-ca58-e9a7-e063-6294a90afd8b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Maximum Strength Medicated Foot Powder Talc Free
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Topco Associates LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-02-10
- Substance
- MENTHOL
- Active strength
- 2.8 g/283g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Menthol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 2.8 g/283g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 259579 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-252-10 | Menthol | 283 g in 1 BOTTLE, PLASTIC | POWDER | 283 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-252 | MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [TOPCO ASSOCIATES LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241213_7caef8db-a07a-6705-e053-2991aa0aa724.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 |
|---|
| 36800-252-10 | 36800025210 | 283 g in 1 BOTTLE, PLASTIC (36800-252-10) | 283 g | 2019-02-10 | 0000-00-00 | No | No | Current |