apgwgzminoxidil2%

Manufacturer
Guangdong Jiaoyu Biotechnology Co., Ltd
Effective date
2026-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-21 02:01:03

Label at a glance#

Productapgwgzminoxidil2%
Active ingredientMINOXIDIL
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only. Do not use if your hair loss is sudden, patchy, or the cause is unknown; you are under 18 years of age; your scalp is red, inflamed, infected, irritated, or painful; or you use other medicines or treatments on the scalp. Ask a doctor before use if you have heart disease. When using this product, apply only to the scalp and avoid contact with eyes. Unwanted facial hair growth may occur. Changes in hair color or texture may occur. It may take 2–4 months to see results, and results vary by individual. Stop use and ask a doctor if chest pain, rapid heartbeat, dizziness, or fainting occurs; sudden weight gain or swelling occurs; severe scalp irritation occurs; or no hair growth occurs after 4 months of use.

INACTIVE INGREDIENT SECTION

Alcohol
Propylene Glycol
Purified Water
Ginseng Botanical Complex
Botanical Scalp Renewal Complex
Herbal Vitality Complex
Phyto-Recovery Complex

INDICATIONS & USAGE SECTION

Helps regrow hair on the scalp

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - PURPOSE SECTION

Hair regrowth treatment for women.

DOSAGE & ADMINISTRATION SECTION

Apply 1 mL directly to the scalp twice daily. Do not exceed the recommended dosage. More frequent use will not improve results. Continued use is necessary to maintain hair regrowth.

RECENT MAJOR CHANGES SECTION

Apply 1 mL directly to the scalp twice daily. Do not exceed the recommended dosage. More frequent use will not improve results. Continued use is necessary to maintain hair regrowth.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 11

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87722-09187722-091-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINOXIDIL5965120SH1ACTIB
WATER059QF0KO0RIACT

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
apgwgzminoxidil2%MINOXIDILGuangdong Jiaoyu Biotechnology Co., Ltd5957c990-e274-6278-e063-6394a90af2b72026-08-18WarningsExact identifier
ndc (package): 87722-091-01
ndc (product): 87722-091
ndc11 (package): 87722009101
spl id: 5957c949-5dc2-956f-e063-6294a90ac22b
spl set id: 5957c990-e274-6278-e063-6394a90af2b7

Reported adverse events (FAERS/openFDA)#

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