Home NDC 87875-001-01 5% MINOXIDIL HAIR REGROWTH SERUM With Biotin
Product NDC 87875-001
Requested package NDC 87875-001-01
11-digit product format 878750001
Labeler code 87875
Product ID 87875-001_570899ce-bb75-b3f1-e063-6294a90a4497
Type HUMAN OTC DRUG
Nonproprietary name 5% Minoxidil
Dosage form LIQUID
Route TOPICAL
Labeler Shenzhen Shengxing Tengda Technology Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-20
Substance MINOXIDIL
Active strength .05 g/mL
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 REGROWTH SERUM With Biotin
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL .05 g/mL
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 87875-001-01 87875000101 2 BOTTLE in 1 BOX (87875-001-01) / 60 mL in 1 BOTTLE 2 bottle 2026-07-20 No No Current