83766-003 5% Minoxidil Hair Growth Sprays Serum

Manufacturer
Shenzhen Joyuflsh Technology Co.,Ltd.
Effective date
2026-05-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:58:42

Label at a glance#

Product5% Minoxidil Hair Growth Sprays Serum
Active ingredientBIOTIN, MINOXIDIL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%
Biotin 0.5%

OTC - PURPOSE SECTION

Hair Regrowth Treatment

INDICATIONS & USAGE SECTION

Use to regrow hair and beard.

WARNINGS SECTION

Keep out of reach of children.

For external use only

OTC - DO NOT USE SECTION


Your hair loss is sudden and/or patchy.
Your hair loss is associated with childbirth
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

Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water.
Some people have experienced changes in hair color and/or texture.

It takes time to regr ow hair. Results may occur at 3 months wth twice a day usage. For some men, you may need to use this product for at least 6 months before you see results. The amount of hair regrowth is different for each person.

Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water

OTC - STOP USE SECTION

Chest pain, rapid heartbeat, faintness, or dizziness occurs

Sudden, unexplained weight gain occurs

If unwanted facial hair growth occurs

If you do not see hair regrowth in 6 months

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away,

DOSAGE & ADMINISTRATION SECTION

1.Make sure your hair and scalp are dry(no need to wash your hair before each use)

2.Apply 3-4 pumps of spray directly to the treated area of the scalp

3.Gently massage into the scalp or thinning hair areas until absorbed.

4.Continued use is required to increase and maintain hair regrowth. Discontinuation may lead to hair loss

INACTIVE INGREDIENT SECTION

Butylene Glycol
Glycerin
Alcohol
Castor oil
Dexpanthenol
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2715603biotin 0.5 % / minoxidil 5 % Topical SprayPSN1
2715603biotin 5 MG/ML / minoxidil 50 MG/ML Topical SpraySCD1
2715603biotin 0.5 % / minoxidil 5 % Topical SpraySY1

DailyMed Pharmacologic Classes#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83766-003-015% Minoxidil Hair Growth Sprays Serum60 mL in 1 BOTTLELIQUID601
83766-003-015% Minoxidil Hair Growth Sprays Serum7 in 1 PACKAGELIQUID71

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83766-00383766-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
5% Minoxidil Hair Growth Sprays SerumMINOXIDIL, BIOTINShenzhen Joyuflsh Technology Co.,Ltd.52b05542-b2fc-b223-e063-6394a90afd3e2026-05-25WarningsExact identifier
ndc (package): 83766-003-01
ndc (product): 83766-003
ndc11 (package): 83766000301
spl id: 52b05542-b2fd-b223-e063-6394a90afd3e
spl set id: 52b05542-b2fc-b223-e063-6394a90afd3e

Reported adverse events (FAERS/openFDA)#

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