BestHealth Menthol
- Product NDC
- 52642-001
- 11-digit product format
- 526420001
- Labeler code
- 52642
- Product ID
- 52642-001_9d4b1b19-c3c0-ed44-e053-2995a90a18c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Bestco Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-12-20
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.