5% Minoxidil Hair Growth Topical Solution

Manufacturer
Yiwu Pu Feather Trading Co., LTD
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:29:38

Label at a glance#

Product5% Minoxidil Hair Growth Topical Solution
Active ingredientMINOXIDIL, BIOTIN
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%
Biotin 0.5%

OTC - PURPOSE SECTION

Hair Regrowth Treatment

INDICATIONS & USAGE SECTION

Use to regrow hair and beard.

WARNINGS SECTION

Keep out of reach of children.

For external use only

OTC - DO NOT USE SECTION

Your hair loss is sudden and/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.
Your scalp is red, inflamed, infected, irritated, or painful.
You use other medicines on the scalp.

OTC - WHEN USING SECTION


Avold contact with the eves. in case of accidental contact, rinse eves with large amounts of cool tap water
Some people have experienced changes in hair color and/or texture.
It takes time to regrow hair. Results may occur at 3 months with twice a day usage. For some men, you may need to use this product for at least 6 months before you see results. The amount of hair regrowth is diferent for each person.
Avoid contact with eyes. in case of accidental contact, rinse eyes with a large amount of cool tap water.

OTC - STOP USE SECTION


Chest pain, rapid heartbeat, faintness, or dizziness occurs.
Sudden, unexplained weight gain occurs.
lf unwanted facial hair growth occurs
lf you do not see hair regrowth in 6 months.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. f swallowed, get medical help or contact a Poison Control Center
(1-800-222-1222)right away.

DOSAGE & ADMINISTRATION SECTION


1. After opening the cap, apply 1 ml by pressing and dotting onto the scalp area to be treated.
2. Gently massage the scalp or sparse hair area until fully absorbed.
3. Use twice daily.
4. Continuous use is necessary to increase and maintain har regrowth. Stopping use may lead to hair loss

INACTIVE INGREDIENT SECTION

Butylene Glycol
Glycerin
Alcohol
Castor oil
Dexpanthenol
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2691097biotin 0.5 % / minoxidil 5 % Topical SolutionPSN1
2691097biotin 5 MG/ML / minoxidil 50 MG/ML Topical SolutionSCD1
2691097biotin 0.5 % / minoxidil 5 % Topical SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MINOXIDIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87112-001-015% Minoxidil Hair Growth Topical Solution80 mL in 1 BOTTLELIQUID801
87112-001-015% Minoxidil Hair Growth Topical Solution3 in 1 PACKAGELIQUID31
87112-001-025% Minoxidil Hair Growth Topical Solution6 in 1 PACKAGELIQUID61
87112-001-025% Minoxidil Hair Growth Topical Solution80 mL in 1 BOTTLELIQUID801

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87112-00187112-001-01, 87112-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
5% Minoxidil Hair Growth Topical SolutionMINOXIDILYiwu Pu Feather Trading Co., LTD473c555b-de13-56d5-e063-6394a90a377f2025-12-31WarningsExact identifier
ndc (package): 87112-001-02
ndc (package): 87112-001-01
ndc (product): 87112-001
ndc11 (package): 87112000102
ndc11 (package): 87112000101
spl id: 473c5ade-27d7-4c51-e063-6394a90a8fb8
spl set id: 473c555b-de13-56d5-e063-6394a90a377f

Reported adverse events (FAERS/openFDA)#

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