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.

DailyMed Socrata Ingredients#