5% MINOXIDIL HAIR GROWTH SERUM liquid

Manufacturer
Hengyang Chuangjiujia Trading Co., Ltd.
Effective date
2025-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:03:25

Label at a glance#

Product5% MINOXIDIL HAIR GROWTH SERUM liquid
Active ingredientMINOXIDIL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Hair regrowth treatment

INDICATIONS & USAGE SECTION

to regrow hair on the scalp

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION


you have no family history of hair loss,hair loss is sudden and/or patchy.
you do not know the reason for your hair loss.
you are under 18 years of age. Do notuse it on babies and children.scalp is red, inflamed, infected, irritated,or painful.
you use other medicines on the scalp

OTC - WHEN USING SECTION


Do not apply on other parts ofthe body.
Avoid contact with eyes. in case ofaccidental contact, rinse eyes witha large amount of cool tap water.
lt takes time to regrow hair. You mayneed to use this product 2 times a day forat least 4 months before you see results The amount of hair regrowth is differentfor each person.
The product will not work for everyone.

OTC - STOP USE SECTION


chest pain, rapid heart beat, faintness,or dizziness occurs.
sudden, unexplained weight gain occurs.
your hands or feet swell.
scalp irritation or redness occurs.
you get unwanted facial hair growth.
you do not see hair regrowth in 4 months.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contacta poison control center right away.

DOSAGE & ADMINISTRATION SECTION


Apply 2-3 drops of serum directly to thescalp in the area to be treated.
Massage into the scalp with your fingersthen wash hands thoroughly.
Using more hair regrowth serum orusing the serum more often will notimprove your results.
Continued use is necessary to increaseand then maintain your hair regrowth.
Discontinuing use may result in hair loss.

INACTIVE INGREDIENT SECTION

Water
Biotin
Dimethyl isosorbide
Acetic acid
Panthenol
Propylene glycol
Niacinamide
Polysorbate 20

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311724minoxidil 5 % Topical SolutionPSN1
311724minoxidil 50 MG/ML Topical SolutionSCD1
311724minoxidil 3 GM per 60 ML Topical SolutionSY1
311724minoxidil 5 % Topical SolutionSY1
311724minoxidil 5 GM per 100 ML Topical SolutionSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84735-012-015% MINOXIDIL HAIR GROWTH SERUM liquid30 mL in 1 BOTTLELIQUID301
84735-012-015% MINOXIDIL HAIR GROWTH SERUM liquid1 in 1 BOXLIQUID11

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84735-01284735-012-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
37e855bb-472d-725a-e063-6394a90aa4b237e855bb-472c-725a-e063-6394a90aa4b22025-06-19WarningsExact identifier
spl id: 37e855bb-472d-725a-e063-6394a90aa4b2
spl set id: 37e855bb-472c-725a-e063-6394a90aa4b2

Reported adverse events (FAERS/openFDA)#

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