5 MINOXIDIL HAIR FOAM WITH BIOTIN

Manufacturer
Dongguan Haiyi Technology Co.,Ltd.
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:25:11

Label at a glance#

Product5 MINOXIDIL HAIR FOAM WITH BIOTIN
Active ingredientGINGER
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ginger root extrac

Inactive ingredient

INACTIVE INGREDIENT SECTION

mi-noxidil,biotin,ginseng rootextract,glyceryl polymethacrylate,cellulose gum, cholesterol, ceramidenp, disodium edta, glyceryl stearate.methylpropanediol,maltodextrin,guaiazulene, ceramide as, ceramideap, arginine, carbomer, ceramide nsceramide ng, tocopherol, dimethylsi-lanol hyaluronate,hydrolyzedsodium hyaluronate, hydrolyzedhyaluronic acid, potassium hyaluro.nate,hyaluronic acid,sodiumhyaluronate crosspolymer, hydroxy-propyltrimonium hyaluronate.sodium hyaluronate dimethylsilanolsodium acetylated hyaluronate.ceramide eop

Purpose section

OTC - PURPOSE SECTION

Natural ingredientsmild formula, suitable for allpeople & daily use;

Foam texture,easy to absorb andnon-sticky

Warning

WARNINGS SECTION

Keep out of reach ofchildren to avoid accidents; lt isrecommended to test the productbehind the ear before using it, avoidcontact with eyes, and discontinueuse immediately if discomfortoccurs.

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.Make sure yourscalp are clean and dry beforeuse;

2.Apply 1 pump of foam directlyto affected area. (lf you don't haveenough foam,2 pump);

3.Gentlymassage with the brush for 1~2minutes until the foam is fully dry;4.For best results, use twice daily andapply directly to scalp.

Dosage

DOSAGE & ADMINISTRATION SECTION

apply it twice aday, every day.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84732-045-012025-07-29C16284748780-13b156c62-2871-fb37-e063-e6dba90a4e07247bc0fc-3ed2-015b-e063-6294a90ad9cc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84732-045-015 MINOXIDIL HAIR FOAM WITH BIOTIN60 mL in 1 BOTTLE, SPRAYSPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84732-0455 MINOXIDIL HAIR FOAM WITH BIOTIN SPRAY [DONGGUAN HAIYI TECHNOLOGY CO.,LTD.]11 package rows20241016_247bc0fc-3ed2-015b-e063-6294a90ad9cc.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84732-04584732-045-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
247bc0fc-3ed3-015b-e063-6294a90ad9cc247bc0fc-3ed2-015b-e063-6294a90ad9cc2024-10-14WarningsExact identifier
spl id: 247bc0fc-3ed3-015b-e063-6294a90ad9cc
spl set id: 247bc0fc-3ed2-015b-e063-6294a90ad9cc

Reported adverse events (FAERS/openFDA)#

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