FDA.reportPublic FDA data

2% WOMEN MINOXIDIL HAIR STRENGTHENING SET

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd
Effective date
2024-07-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:57:54

Label at a glance#

Product2% WOMEN MINOXIDIL HAIR STRENGTHENING SET
Active ingredientMINOXIDIL
Label structure11 sections

Indications and uses

Keep scalp clean or dry before use. Press the pump head 6 times (1ml) to the scalp. Massage gently for 3-5 minutes, twice a day. Wash your hands after use.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

MINOXIDIL 2%

Purpose

OTC - PURPOSE SECTION

Hair growth

Uses

INDICATIONS & USAGE SECTION

Keep scalp clean or dry before use.
Press the pump head 6 times (1ml) to the scalp.
Massage gently for 3-5 minutes, twice a day.
Wash your hands after use.

Warnings

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Dosage

DOSAGE & ADMINISTRATION SECTION

Press the pump head 6 times (1ml) to the scalp.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER 52.38%
ALCOHOL 30%
PROPYLENE GLYCOL 10%
BUTYLENE GLYCOL 5%
PHENOXYETHANOL 0.54%
ETHYLHEXYLGLYCERIN 0.06%
DISODIUM EDTA 0.02%

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-5552% WOMEN MINOXIDIL HAIR STRENGTHENING SET (MINOXIDIL) LIQUID [GUANGDONG AIMU BIOLOGICAL TECHNOLOGY CO., LTD]1Unmatched20240731_1e822d4e-5826-186f-e063-6394a90a302a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-55583566-555-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALCOHOL3K9958V90MIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
MINOXIDIL5965120SH1ACTIB
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
DIPROPYLENE GLYCOLE107L85C40IACT

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3655dc2f-3fca-06b3-e063-6394a90ae5b81e822d4e-5826-186f-e063-6394a90a302a2025-05-30WarningsExact identifier
spl set id: 1e822d4e-5826-186f-e063-6394a90a302a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.