Mentholatum
- Product NDC
- 72988-0031
- 11-digit product format
- 729880031
- Labeler code
- 72988
- Product ID
- 72988-0031_ffcab802-a76f-e425-e053-6294a90acf76
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Methyl Salicylate, DL-Menthol
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Lydia Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-09-30
- Substance
- MENTHOL; METHYL SALICYLATE
- Active strength
- 60; 200 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mentholatum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 60 mg/g |
| METHYL SALICYLATE | 200 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, LAV5U5022Y |
| Rxcui | 282812 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72988-0031-1 | Mentholatum | 75 g in 1 BOTTLE | LOTION | 75 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72988-0031 | MENTHOLATUM (METHYL SALICYLATE, DL-MENTHOL) LOTION [LYDIA CO., LTD.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230819_e9db590f-b19a-3fe8-e053-2995a90a4e74.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 |
|---|
| 72988-0031-1 | 72988003101 | 75 g in 1 BOTTLE (72988-0031-1) | 75 g | 2022-09-30 | 0000-00-00 | No | No | Current |