Biofreeze Professional
- Product NDC
- 68071-4589
- 11-digit product format
- 680714589
- Labeler code
- 68071
- Product ID
- 68071-4589_7782cdf0-365d-421d-e053-2a91aa0af366
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-06-03
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record