PharmapureRx Menthotral
- Product NDC
- 59088-587
- 11-digit product format
- 590880587
- Labeler code
- 59088
- Product ID
- 59088-587_9f30958e-2a0e-4a06-a834-1cba30bdf3c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- lidocaine, menthol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-08-03
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE ANHYDROUS; MENTHOL
- Active strength
- 39 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-587 | PHARMAPURERX MENTHOTRAL (LIDOCAINE, MENTHOL) CREAM [PURETEK CORPORATION] | 3 | Legacy NDC | 20241004_d2a9aeb6-8a94-49e7-ab46-84403560b6c8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59088-587-16 | 59088058716 | 237 mL in 1 BOTTLE, PUMP (59088-587-16) | 237 ml | 2017-08-03 | 0000-00-00 | No | No | Current |