Home NDC 84232-003 HAIR REGEN HAIR REGROWTH TREATMENT
Product NDC 84232-003
11-digit product format 842320003
Labeler code 84232
Product ID 84232-003_2b2e6e17-cd97-278d-e063-6394a90a6a82
Type HUMAN OTC DRUG
Nonproprietary name Womens Liquid Minoxidil 1pk
Dosage form LIQUID
Route TOPICAL
Labeler YIWU�YIZHOU�TRADING�CO.,LTD
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-01-08
Substance MINOXIDIL
Active strength 2 g/100mL
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 HAIR REGEN HAIR REGROWTH TREATMENT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 2 g/100mL
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 311723 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84232-003-01 HAIR REGEN HAIR REGROWTH TREATMENT 60 mL in 1 BOTTLE LIQUID 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84232-003 HAIR REGEN HAIR REGROWTH TREATMENT (WOMENS LIQUID MINOXIDIL 1PK) LIQUID [YIWU YIZHOU TRADING CO.,LTD] 3 Current NDC, 1 package rows 20250109_29ae9a7a-a692-e2c1-e063-6294a90a60e3.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84232-003-01 84232000301 60 mL in 1 BOTTLE (84232-003-01) 60 ml 2025-01-08 No No Current