EXDEPLOY 5% Minoxidil Topical Gel

Manufacturer
Guangzhou Ruijiu Electronic Technology Co., Ltd.
Effective date
2024-04-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:10:47

Label at a glance#

ProductEXDEPLOY 5% Minoxidil Topical Gel
Active ingredientMINOXIDIL
Label structure13 sections

Storage and handling

Read all information on the box before use. Keep the box. It contains important information. Store at a controlled room temperature of 10 to 30°C(50 to 86°F). Ensure that the lid remains closed. Do not store at temperatures above 40°C(104°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

EXDEPLOY 5% MINOXIDIL TOPICAL GEL

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Hair regrowth treatment

INDICATIONS & USAGE SECTION

to regrow hair on the scalp

WARNINGS SECTION

For externaluse only.

OTC - DO NOT USE SECTION

Your amount of hair loss is different than that shown the side of this carton, 5% Minoxidil Gel is not intended for fronta baldness or receding hairline.
Your hair loss is sudden and/or patch.
You do not know the reason for your hair loss.
You are under 18years 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

Do not apply on other parts of the body. Avoid contact with eyes.In case of accidental contact,rinse eyes with a large amount of cool tap water lt takes time to regrow hair.
You may need to use this product 1 times a day for at least 3 months before you see results, The amount of hair regrowth is different for each person.The product will not work for everyone.

OTC - STOP USE SECTION

lf scalp irritation or redness occurs. If you get unwanted facialhair growth. lf you do not see hair regrowth in 4 months.lfsudden, unexplained weight gain occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222

DOSAGE & ADMINISTRATION SECTION

Keep the bottle open by turning the cap. Squeeze bottlegently when using. Apply 3-5 drops of minoxidil gel directlyto the scalp in the area to be treated.
Just apply it with the tip of the bottle and spread it out, you don't
even need to massage it in with your hands. lt's very easy to use.
Rotate the cap to reseal the bottle.
Using more often or increasing the amount will not improveresults; consistent use is essential to promote and maintainhair regrowth.

STORAGE AND HANDLING SECTION

Read all information on the box before use.
Keep the box. It contains important information.
Store at a controlled room temperature of 10 to 30°C(50 to 86°F).
Ensure that the lid remains closed. Do not store at temperatures above 40°C(104°F).

INACTIVE INGREDIENT SECTION

Alcohol
Glycerin
Anhydrous citric acid
Butylated hydroxytoluene
Lactic acid
Polysorbate 60
Biotin
Carbomer homopolymer
Trolamine
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel2label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2668433minoxidil 5 % Topical GelPSN2
2668433minoxidil 0.05 MG/MG Topical GelSCD2
2668433minoxidil 5 % Topical GelSY2

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83767-201-012026-01-29C16284748780-149896155-cd5a-586f-e063-e6dba90add90EXDEPLOY 5% MINOXIDIL TOPICAL GEL
83767-201-022026-01-29C16284748780-149896155-cd5a-586f-e063-e6dba90add90EXDEPLOY 5% MINOXIDIL TOPICAL GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83767-201-01EXDEPLOY 5% Minoxidil Topical Gel60 g in 1 CANGEL602
83767-201-01EXDEPLOY 5% Minoxidil Topical Gel2 in 1 BOXGEL22
83767-201-02EXDEPLOY 5% Minoxidil Topical Gel3 in 1 BOXGEL32
83767-201-02EXDEPLOY 5% Minoxidil Topical Gel60 g in 1 CANGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83767-201EXDEPLOY 5% MINOXIDIL TOPICAL GEL (MINOXIDIL) GEL [GUANGZHOU RUIJIU ELECTRONIC TECHNOLOGY CO., LTD.]24 package rows20240410_1321fb7f-864b-2ef0-e063-6294a90ad284.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
83767-20183767-201-01, 83767-201-02

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
15a56eb3-f813-4554-e063-6294a90aa3d01321fb7f-864b-2ef0-e063-6294a90ad2842024-04-09WarningsExact identifier
spl id: 15a56eb3-f813-4554-e063-6294a90aa3d0
spl set id: 1321fb7f-864b-2ef0-e063-6294a90ad284

Reported adverse events (FAERS/openFDA)#

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