Home NDC 85304-003 Kweqdsd 5% Minoxidil Hair Growth Sprays Serum
Product NDC 85304-003
11-digit product format 853040003
Labeler code 85304
Product ID 85304-003_33bf0180-3a15-683b-e063-6394a90ae911
Type HUMAN OTC DRUG
Nonproprietary name Minoxidil 5%
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Borderless Technology Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-27
Substance MINOXIDIL; BIOTIN
Active strength 5; .5 g/100mL; 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 Kweqdsd 5% Minoxidil Hair Growth Sprays Serum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 g/100mL BIOTIN .5 g/100mL
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 6SO6U10H04 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2715603 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 85304-003-01 Kweqdsd 5% Minoxidil Hair Growth Sprays Serum 3 in 1 PACKAGE LIQUID 3 1 85304-003-01 Kweqdsd 5% Minoxidil Hair Growth Sprays Serum 100 mL in 1 BOTTLE LIQUID 100 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85304-003 KWEQDSD 5% MINOXIDIL HAIR GROWTH SPRAYS SERUM (MINOXIDIL 5%) LIQUID [GUANGZHOU BORDERLESS TECHNOLOGY CO., LTD.] 1 Current NDC, 2 package rows 20250429_33bf0180-3a14-683b-e063-6394a90ae911.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 85304-003-01 85304000301 3 BOTTLE in 1 PACKAGE (85304-003-01) / 100 mL in 1 BOTTLE 3 bottle 2025-04-27 No No Current