Home NDC 87745-002-01 COUGH DROPS- menthol granule
Product NDC 87745-002
Requested package NDC 87745-002-01
11-digit product format 877450002
Labeler code 87745
Product ID 87745-002_563ee31a-f76d-339a-e063-6294a90acb3b
Type HUMAN OTC DRUG
Nonproprietary name menthol granule
Dosage form LOZENGE
Route ORAL
Labeler Anhui Jiuhe Health Industry Co., Ltd
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-03
Substance MENTHOL
Active strength 10.4 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base COUGH DROPS- menthol granule
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 10.4 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 73 of 178 · 3,551 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87745-002-01 87745000201 25 LOZENGE in 1 BOTTLE (87745-002-01) 25 lozenge 2026-06-03 No No Current