FDA.reportPublic FDA data

87813-001 Minoxidil Hair Regrowth Kit

Manufacturer
Guangzhou Zeus E-commerce Co., Ltd
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:36:15

Label at a glance#

ProductMinoxidil Hair Regrowth Kit
Active ingredientMINOXIDIL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Hair regrowth treatment for men

INDICATIONS & USAGE SECTION

Use to regrow hair of scalp and beard

WARNINGS SECTION

For external use only.
Keep out of reach of children.

OTC - DO NOT USE SECTION

You have no family history of hair loss.
Your hair loss is sudden or patchy.
Your hair loss is associated with childbirth.
You do not know the reason for your hair loss.
You are under 18 years of age.Do not use on babies and children.
Our scalp is red, inflamed, infected, or painful.
You use other medicines on the scalp.

OTC - WHEN USING SECTION


Ask doctor before use if you have heart disease.
Avoid contact with eyes. In case of accidental contact,rinse eyes with a large amount of cool tap water.

OTC - STOP USE SECTION

· If scalp irritation or redness occurs.
· If you get unwanted facial hair growth.
· If you do not see hair regrowth in 4 months.
·If sudden unexplained weight gain occurs.
·If swallowed, get medical help or contact a poison control center(1-800-222-1222)right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Apply the roll-on solution directly tothe clean and dry scalp in thehair loss area. Roll evenly over thedesired area 4-5 times, then gentlymassage with fingertips for2-3 minutes to help absorption.Do not rinse.Use 1-2 times daily.Allow the scalp to dry completelybefore applying any otherhair products. Wash hands thoroughlyafter use. Do not exceed 2 mL per day.Continued use for several months isnecessary to help increase andmaintain hair regrowth.

INACTIVE INGREDIENT SECTION

AQUA
DIPROPYLENE GLYCOL
DISODIUM EDTA
ALCOHOL
PROPYLENE GLYCOL
BUTYLENE GLYCOL
NIACINAMIDE
BIOTIN
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
ALOE BARBADENSIS LEAF JUICE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87813-00187813-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
AQUA059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
NIACINAMIDE25X51I8RD4IACT
ALCOHOL3K9958V90MIACT
MINOXIDIL5965120SH1ACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
BIOTIN6SO6U10H04IACT
DIPROPYLENE GLYCOLE107L85C40IACT
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE DISODIUM7FLD91C86KIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT

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
Minoxidil Hair Regrowth KitMINOXIDILGuangzhou Zeus E-commerce Co., Ltd550bce76-4c78-80f0-e063-6394a90ad58f2026-06-24WarningsExact identifier
ndc (package): 87813-001-01
ndc (product): 87813-001
ndc11 (package): 87813000101
spl id: 550bce76-4c79-80f0-e063-6394a90ad58f
spl set id: 550bce76-4c78-80f0-e063-6394a90ad58f

Reported adverse events (FAERS/openFDA)#

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