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MINOXIDIL 5% TOPICAL AEROSOL60g drug information

MINOXIDIL
Shenzhen Joyuflsh Technology Co.,Ltd. · TOPICAL

Product NDC: 83766-005

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameMINOXIDIL
Labeler / manufacturerShenzhen Joyuflsh Technology Co.,Ltd.
RouteTOPICAL
Drug classArteriolar Vasodilator
Product NDC83766-005
Label effective date2026-08-27

Official product label reference

MINOXIDIL 5% TOPICAL AEROSOL60g — Shenzhen Joyuflsh Technology Co.,Ltd.

This page contains 10 source sections for MINOXIDIL, topical route. Label set 5a03675b-0bfd-7058-e063-6294a90acf4d, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use to regrow hair on the top of the scalp

Purpose

Hair regrowth treatment
Dosage and administration — label text
See enclosed leaflet for complete directions on how to use. Apply half a capful twice daily directly to the scalp in the hair loss area. Massage into scalp with fingers, then wash hands well. Using more or more often will not improve results. Continued use is necessary to increase and keep your hair regrowth or hair loss will begin again. Men:use twice daily.Women:use once daily.
Warnings
For external use only. Extremely Flammable:Avoid fire, flame, or smoking during and immediately following application.
Active ingredient
Minoxidil 5% Biotin 0.5%
Do not use
Your amount of hair loss is different than that shown on side of this carton or your hair loss is on the front of the scalp. 5% minoxidil foam is not intended for frontal baldness or receding hairline. You have no family history of hair loss. Your hair loss is sudden and/or patchy. You do not know the reason for vour hair loss. You are under 18 years of age. Do not use on babies and children. You use other medicines on the scalp. Your scalp is red, inflamed, infected, irritated, or painful.
When to stop use and seek help
if chest pain, rapid heartbeat, faintness, or dizziness occurs. if sudden, unexplained weight gain occurs. if your hands or feet swell. if scalp irritation or redness occurs. if unwanted facial hair growth occurs. if you do not see hair regrowth in 6 months.
While using this medicine
Do not apply on other parts of the body. Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cooltap water. Some people have experienced changes in hair color and/or texture it takes time to regrow hair.Results may occur at 3 months with twice a day usage. For some people, 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. This product will not work for all people.
Child safety
If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222) right away.
Inactive ingredient
Cetyl alcohol Citric acid Glycerin Isobutane Lactic acid Polysorbate 60 Purified water SD alcohol Stearyl alcohol Butane Edetate disodium

Official sources and product identifiers

Substances listed: MINOXIDIL, BIOTIN

RxNorm identifiers: 2723100

Package NDC codes

83766-005-01, 83766-005-02

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.