5% minoxidil hair regrowth treatment

Manufacturer
Shenzhen Baixingchen Technology Co., Ltd.
Effective date
2023-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:58:10

Label at a glance#

Product5% minoxidil hair regrowth treatment
Active ingredientMINOXIDIL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - ASK DOCTOR SECTION

Ask a Doctor before use if you
have Heart disease.

WARNINGS SECTION

Warnings
-For external use only.
-Keep away from fire and flame.
-Avoid contact with eyes.

OTC - DO NOT USE SECTION

Do not use
-You have no family history of hair loss,hair loss is sudden and/orpatchy.
-You do not know the reason for your hair loss.
-You are under 18 years of age.
Do not use it on babies and children.
-Your scalp is red,inflamed, infect-edirritated,or painful.
-You use other medicines on the scalp.

OTC - WHEN USING SECTION

When using
-Do not apply on other parts of the body.
-void contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water.
-It takes time to regrow hair. You may need to use this product 2 times a day for a least 4 months before you see results, The amount of hair regrowth is different for each person

OTC - STOP USE SECTION

Stop use and ask doctor if
-chest pain,rapid heart beat,faintness,or dizziness occurs sudden, unexplained weight gain occurs your hands or feet swell scalp irritation or redness occurs
-May be harmful when pregnant or breast-feeding

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 right away. (1-800-222-1222)

OTC - PURPOSE SECTION

Hair Regrowth Treatment

OTHER SAFETY INFORMATION

Other information
-Before use, read all information on the carton.
-Store at controlled room temperature 20 to 25 ℃ (68 to 77°F)

DOSAGE & ADMINISTRATION SECTION

Directions
-Apply 1ml (7 Sprays) twice a day.
Once in the morning and another time in the evening before bed.
-Spray directly on top of the scalp in the area to be treated.
-Using more than directed or more often will not improve results.
-Continued use is necessary to increase and then maintain your hair regrowth.
-Discontinuing use may result in hair loss.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Propylene Glycol, Ethyl Alcohol, Aqua.

INDICATIONS & USAGE SECTION

Use to regrow hair on the top of the scalp.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABELPACKAGE LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1537948minoxidil 5 % Topical SprayPSN1
1537948minoxidil 50 MG/ML Topical SpraySCD1
1537948minoxidil 5 % Topical SpraySY1

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83648-002-012025-01-30C16284748780-11030e365-37e3-111a-e063-dadaa90a10e208c6d31f-f685-63e9-e063-6394a90a04b4
83648-002-012024-01-30C16284748780-11030e365-37e3-111a-e063-dadaa90a10e208c6d31f-f685-63e9-e063-6394a90a04b4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83648-002-015% minoxidil hair regrowth treatment60 mL in 1 BOTTLESPRAY601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83648-0025% MINOXIDIL HAIR REGROWTH TREATMENT (SANNUO 5% MINOXIDIL HAIR REGROWTH TREATMENT) SPRAY [SHENZHEN BAIXINGCHEN TECHNOLOGY CO., LTD.]11 package rows20231030_08c6d31f-f685-63e9-e063-6394a90a04b4.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83648-00283648-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
MINOXIDIL5965120SH1ACTIB
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT

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
08c6d31f-f686-63e9-e063-6394a90a04b408c6d31f-f685-63e9-e063-6394a90a04b42023-10-28WarningsExact identifier
spl id: 08c6d31f-f686-63e9-e063-6394a90a04b4
spl set id: 08c6d31f-f685-63e9-e063-6394a90a04b4

Reported adverse events (FAERS/openFDA)#

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