Minoxidil Hair Growth Serum

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:36:27

Label at a glance#

ProductMinoxidil Hair Growth Serum
Active ingredientMINOXIDIL
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

Inactive ingredient

INACTIVE INGREDIENT SECTION

Biotin, Water, Propylene Glycol,Dimethyl lsosorbide, Ethanol, Panthenol,Niacinamide,Polysorbate 20, Aloe Vera Extract,PEG-40 Hydrogenated Castor Oil, Hydrolysed Collagen

Purpose section

OTC - PURPOSE SECTION

  1. Activate hair follicles
  2. Stimulates hair growvth
  3. Strengthen the roots of the hair
  4. Gentle and effectively stimulates hairgrowth for both men and women

Warning

WARNINGS SECTION

  1. This product is a hair growth solution, notallowed to be eaten, it is recommended to bekept out of the reach of children toavoid accidental ingestion, if aocidentallyingested please contact a health professional formedical attention immediately
  2. If hair loss is very serious, please do not use itblindly in large quantities and go to the hospitalfor treatment in time!

stop use

OTC - STOP USE SECTION

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

OTC - DO NOT USE SECTION

Not suitable for use by children, pregnantor breast feeding people.

OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

INDICATIONS & USAGE SECTION

  1. Wash hair and scalp before use, then apply 2-3 drops of serum to the parts of the scalp where hair needs to grow
  2. Gently massage the scalp with your fingertips, which can be combined with head acupressure for better results, for 1~2 minutes until the serum is completety dry.
  3. After the massage, hands can be cleaned.

Dosage

DOSAGE & ADMINISTRATION SECTION

*Products need to be used continuously toincrease and maintain hair regeneration,<discontinuing the product may result in hair loss

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-089-012025-07-29C16284748780-13b156c62-2c97-fb37-e063-e6dba90a4e0726721c96-eecd-5cce-e063-6394a90a1e35

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-089-01Minoxidil Hair Growth Serum60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-089MINOXIDIL HAIR GROWTH SERUM LIQUID [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20241110_26721c96-eecd-5cce-e063-6394a90a1e35.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84732-08984732-089-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
26721c96-eece-5cce-e063-6394a90a1e3526721c96-eecd-5cce-e063-6394a90a1e352024-11-08WarningsExact identifier
spl id: 26721c96-eece-5cce-e063-6394a90a1e35
spl set id: 26721c96-eecd-5cce-e063-6394a90a1e35

Reported adverse events (FAERS/openFDA)#

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