5% Minoxidil Spray

Manufacturer
Shenzhen Lancity Information Technology Co., Ltd
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:33

Label at a glance#

Product5% Minoxidil
Active ingredientMINOXIDIL
Label structure9 sections

Storage and handling

Storage conditions: Please storein a cool and dry place to avoiddirect sunlight

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Effective Solution
ForHair Thinning And Breakage
Make Hair Thicker Tealthier

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out ofreach of children

INDICATIONS & USAGE SECTION

1.Keep scalp clean and dry before use
2.Brush the hair and spray 6-7 times (about lml) on the scalp on the area of use
3.Massage the affected area for 3-5 minutes to allow the solution to absorb thoroughly
4.Wash hands after use to avoidcontamination with other items

WARNINGS SECTION

1.External use, not internal, avoiddirect contact with the eyes, such asaccidentallyinto the eyes, that is,wash with water ;
2. Keep out ofreach of children
3. If you feelunwell, stop using it.

DOSAGE & ADMINISTRATION SECTION

Brush the hair and spray 6-7 times (about lml) on the scalpon the area of use

STORAGE AND HANDLING SECTION

Storage conditions: Please storein a cool and dry place to avoiddirect sunlight

INACTIVE INGREDIENT SECTION

Water
phenoxyethanol
turmeric extract
castor oil
ginseng extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel2label2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83889-101-012025-07-29C16284748780-13b156c62-2c8b-fb37-e063-e6dba90a4e075% Minoxidil Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83889-101-015% Minoxidil60 mL in 1 BOTTLEOIL602
83889-101-015% Minoxidil1 in 1 BOXOIL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83889-1015% MINOXIDIL (MINOXIDIL) OIL [SHENZHEN LANCITY INFORMATION TECHNOLOGY CO., LTD]22 package rows20241031_0d14dbe6-35a6-5849-e063-6394a90a49b8.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83889-10183889-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
25af14e9-d356-d1b1-e063-6394a90ab3f40d14dbe6-35a6-5849-e063-6394a90a49b82024-10-30WarningsExact identifier
spl id: 25af14e9-d356-d1b1-e063-6394a90ab3f4
spl set id: 0d14dbe6-35a6-5849-e063-6394a90a49b8

Reported adverse events (FAERS/openFDA)#

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