Home NDC 85992-007 5% Minoxidil Hair Growth Serum Roll-on
Product NDC 85992-007
11-digit product format 859920007
Labeler code 85992
Product ID 85992-007_57e4ccae-798a-a36e-e063-6394a90a9927
Type HUMAN OTC DRUG
Nonproprietary name Minoxidil 5% , Rosemary 1%
Dosage form LIQUID
Route TOPICAL
Labeler Shenzhen Boyimei Technology Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-31
Substance MINOXIDIL; ROSEMARY
Active strength .05; .01 g/mL; 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 Growth Serum Roll-on
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL .05 g/mL ROSEMARY .01 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5965120SH1 Internal UNII lookup IJ67X351P9 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 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 85992-007-01 85992000701 3 BOTTLE in 1 BOX (85992-007-01) / 25 mL in 1 BOTTLE 3 bottle 2026-07-31 No No Current 85992-007-02 85992000702 4 BOTTLE in 1 BOX (85992-007-02) / 25 mL in 1 BOTTLE 4 bottle 2026-07-31 No No Current