PAIN RELIEF
- Product NDC
- 82687-101
- 11-digit product format
- 826870101
- Labeler code
- 82687
- Product ID
- 82687-101_dead8732-1ef7-0a3e-e053-2a95a90af4ae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- VIASOX LTD
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-04-26
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 11 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82687-101-13 | 82687010113 | 90 mL in 1 BOTTLE, WITH APPLICATOR (82687-101-13) | 90 ml | 2022-04-26 | 0000-00-00 | No | No | Current |