DIZOP 5% Minoxidil Topical Gel

Manufacturer
Shenzhen Joyuflsh Technology Co.,Ltd.
Effective date
2024-04-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:10:47

Label at a glance#

ProductDIZOP 5% Minoxidil Topical Gel
Active ingredientMINOXIDIL
Label structure13 sections

Storage and handling

Before use, read all information on the carton. Keep the carton. It contains important information. Store at a controlled room temperature of 5 to 30 C (41 to 86°F). Kindly ensure the lid remains closed. Do not store at temperatures above 40C(104°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DIZOP 5% Minoxidil Topical Gel

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Hair regrowth treatment

INDICATIONS & USAGE SECTION

Apply 3-4 drops of Minoxidil Gel directly to the scalp in the area to be treated.
Massage into the scalp with your fingers then wash hands thoroughly.
Using more or using more often will not improve results; continued use is necessary to promote and maintain hair regrowth.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Your amount of hair loss is different than that shown the side of this carton or your hair loss is on the front of the scalp. 5% Minoxidil Gel is not intended for frontal baldness or receding hairline.
you have no family history of hair loss.
your hair loss is sudden and/or patch.
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

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. lf you get unwanted facial hair growth. lf you do not see hair regrowth in 4 months.lf sudden, unexplained weight gain occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222

DOSAGE & ADMINISTRATION SECTION

Apply 3-4 drops of Minoxidil Gel directly to the scalp in the area to be treated.

Massage into the scalp with your fingers then wash hands thoroughly.

Using more or using more often will not improve results; continued use is necessary to promote and maintain hair regrowth.

STORAGE AND HANDLING SECTION

Before use, read all information on the carton.
Keep the carton. It contains important information.
Store at a controlled room temperature of 5 to 30 C (41 to 86°F).
Kindly ensure the lid remains closed. Do not store at temperatures above 40C(104°F).

INACTIVE INGREDIENT SECTION

Minoxidil
ALCOHOL
GLYCERIN
CETYL ALCOHOL
MYRISTYL LACTATE
POLYSORBATE 60
SODIUM THIOSULFATE
CARBOMER HOMOPOLYMER
TROLAMINE
WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1label2label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2668433minoxidil 5 % Topical GelPSN3
2668433minoxidil 0.05 MG/MG Topical GelSCD3
2668433minoxidil 5 % Topical GelSY3

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
4073022c-5d5d-48f5-82ed-091ad146a4b2Product name120171211
9ffbd0ae-0bce-c086-b707-f0da5f8cd7c5Product name120150828

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83766-102-01DIZOP 5% Minoxidil Topical Gel60 g in 1 CANISTERGEL603
83766-102-01DIZOP 5% Minoxidil Topical Gel2 in 1 PACKAGEGEL23
83766-102-02DIZOP 5% Minoxidil Topical Gel3 in 1 PACKAGEGEL33
83766-102-02DIZOP 5% Minoxidil Topical Gel60 g in 1 CANISTERGEL603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83766-102DIZOP 5% MINOXIDIL TOPICAL GEL (MINOXIDIL) GEL [SHENZHEN JOYUFLSH TECHNOLOGY CO.,LTD.]34 package rows20240410_0f222722-fa6b-ceb9-e063-6294a90ae096.zip

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
83766-10283766-102-01, 83766-102-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
15a5551f-e63a-6356-e063-6394a90a127a0f222722-fa6b-ceb9-e063-6294a90ae0962024-04-09WarningsExact identifier
spl id: 15a5551f-e63a-6356-e063-6394a90a127a
spl set id: 0f222722-fa6b-ceb9-e063-6294a90ae096

Reported adverse events (FAERS/openFDA)#

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