Menthol
- Product NDC
- 50488-1040
- 11-digit product format
- 504881040
- Labeler code
- 50488
- Product ID
- 50488-1040_d452ca4e-4a2f-410d-9b15-4c87d3904d91
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Alexso, Inc
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-04-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 40 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50488-1040-1 | Menthol | 120 g in 1 BOTTLE | CREAM | 120 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50488-1040 | MENTHOL CREAM [ALEXSO, INC] | 2 | Legacy NDC, 1 package rows | 20190420_ebfd4e87-3dd4-4db0-a26b-3a11a9811886.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 |
|---|
| 50488-1040-1 | 50488104001 | 120 g in 1 BOTTLE (50488-1040-1) | 120 g | 2019-04-01 | 0000-00-00 | No | No | Current |