Menthol and Zinc Oxide
- Product NDC
- 10135-701
- 11-digit product format
- 101350701
- Labeler code
- 10135
- Product ID
- 10135-701_4527ab64-b939-8e53-e063-6294a90a07a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol and Zinc Oxide
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Marlex Pharmaceuticals, Inc.
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-05-01
- Substance
- MENTHOL; ZINC OXIDE
- Active strength
- .44; 20.625 g/100g; 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
- Menthol and Zinc Oxide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | .44 g/100g |
| ZINC OXIDE | 20.625 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, SOI2LOH54Z |
| Rxcui | 2123045 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10135-701-04 | Menthol and Zinc Oxide | 113 g in 1 TUBE | OINTMENT | 113 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-701 | MENTHOL AND ZINC OXIDE OINTMENT [MARLEX PHARMACEUTICALS, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241010_c24e2dab-cab4-38f4-e053-2995a90aabae.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 |
|---|
| 10135-701-04 | 10135070104 | 113 g in 1 TUBE (10135-701-04) | 113 g | 2021-05-01 | 0000-00-00 | No | No | Current |