MENTHOL
- Product NDC
- 72937-004
- 11-digit product format
- 729370004
- Labeler code
- 72937
- Product ID
- 72937-004_44141d2a-1d91-b970-e063-6294a90a53f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SUNSET PAIN RELIEF ROLL-ON 3OZ
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-09-24
- Marketing end
- 2026-10-23
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 4 g/100mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MENTHOL
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL, UNSPECIFIED FORM | 4 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72937-004-03 | MENTHOL | 90 mL in 1 BOTTLE, WITH APPLICATOR | GEL | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72937-004 | MENTHOL GEL [SUNSET PAIN RELIEF ROLL-ON 3OZ] | 3 | Current NDC, 1 package rows | 20240129_934d4638-b47b-187d-e053-2995a90ae69d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72937-004-03 | 72937000403 | 90 mL in 1 BOTTLE, WITH APPLICATOR (72937-004-03) | 90 ml | 2019-09-24 | 2026-10-23 | No | No | Historical |