Home NDC 87710-003-01 5% Minoxidil hair growth Serum
Product NDC 87710-003
Requested package NDC 87710-003-01
11-digit product format 877100003
Labeler code 87710
Product ID 87710-003_597582b0-cfcd-f7b7-e063-6394a90a0e9a
Type HUMAN OTC DRUG
Nonproprietary name MINOXIDIL
Dosage form LIQUID
Route CUTANEOUS
Labeler Guangzhou Huanmei Cosmetics Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-08-20
Substance MINOXIDIL
Active strength 5 mg/100mg
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
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 5% Minoxidil hair growth Serum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5965120SH1 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 311724 Internal RxNorm 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87710-003-01 87710000301 2 BOTTLE in 1 BOX (87710-003-01) / 60 mg in 1 BOTTLE 2 bottle 2026-08-20 No No Current