Kemagel Pain Relief
- Product NDC
- 28691-1010
- 11-digit product format
- 286911010
- Labeler code
- 28691
- Product ID
- 28691-1010_f3510d60-9a34-48b4-ba9b-6a286bc2d406
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Pharmaplast SAE
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-09-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 10 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record