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EITIKO Minoxidil Hair Regrowth Treatment drug information

MINOXIDIL
Guangzhou Ariel Medical Technology Co., Ltd. · TOPICAL

Product NDC: 87815-006

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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 / manufacturerGuangzhou Ariel Medical Technology Co., Ltd.
RouteTOPICAL
Drug classArteriolar Vasodilator
Product NDC87815-006
Label effective date2026-09-04

Official product label reference

EITIKO Minoxidil Hair Regrowth Treatment — Guangzhou Ariel Medical Technology Co., Ltd.

This page contains 12 source sections for MINOXIDIL, topical route. Label set 5aa2a552-f8b5-f11a-e063-6394a90abb1a, 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 scalp

Purpose

Hair regrowth treatment
Dosage and administration — label text
Directions Apply 1 mL with the dropper directly onto the scalp in the hair loss area as directed. Do not use more than directed. Use twice daily, once in the morning and once at night.
Warnings
For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Keep out of reach of children. Discontinue use if any irritation or adverse reaction occurs. If you are pregnant, nursing, or have any underlying medical conditions, consult your healthcare provider before using the product.
Active ingredient
5% Minoxidil
Do not use
Do not use if you are under 18 years of age. Do not use on babies and children. your scalp is red, inflamed, infected, irritated, or painful. your hair loss is sudden and/or patchy. you do not know the reason for your hair loss. you use other medicines on the scalp.
While using this medicine
apply only to the scalp. avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water. using more or more often will not improve results. continued use is necessary to maintain hair regrowth.
When to stop use and seek help
Stop use and ask a doctor if chest pain, rapid heartbeat, faintness, or dizziness occurs. sudden, unexplained weight gain occurs. your hands or feet swell. scalp irritation or redness occurs. unwanted facial hair growth occurs. other serious or persistent adverse reactions occur
Child safety
Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredient
Alcohol Denat., Propylene Glycol, Water, Aloe Barbadensis Leaf Water, Rosmarinus Officinalis (Rosemary) Leaf Extract, 1,2-Hexanediol, Polyglycerin-10, Dipotassium Glycyrrhizate, Niacinamide, Butylene Glycol, Sodium Polyglutamate, Caffeine, Cyclodextrin, Phenoxyethanol, Biotin, Ethylhexylglycerin
Unclassified section
Formulated in USA Distributed by Guangzhou Hejin Biotechnology Co., Ltd. Address: Room 720, Commercial Unit, No.1, East Huijing 2nd Street, Huadu District, Guangzhou City Labeler: Guangzhou Ariel Medical Technology Co., Ltd.
Other safety information
Other Information: Store at controlled room temperature 20 ° to 25°C (68° to 77°F). Keep tightly closed. Keep away from excessive heat and direct sunlight. Before use, read all information on the carton. Keep the carton. It contains important information.

Official sources and product identifiers

Substances listed: MINOXIDIL

RxNorm identifiers: 311724

Package NDC codes

87815-006-01

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.