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Minoxidil Hair Growth Serum

minoxidil · Minoxidil Hair Growth Serum is an arteriolar vasodilator (over-the-counter) containing minoxidil, made by 2 manufacturers.

Type
Over the counter
Drug class
Arteriolar Vasodilator
Route
Topical
Manufacturers
2

To regrow hair on the scalp

Drug facts

Generic name
minoxidil
Active ingredients
Minoxidil
Drug class
Arteriolar Vasodilator
Dosage forms
Liquid
Label holder
Guangzhou Ariel Medical Technology Co., Ltd.
FDA application
505G(a)(3)
Label updated
07/01/2026

Active ingredients

5% Minoxidil

Purpose

Hair growth treatment

Uses

To regrow hair on the scalp

Directions

Use the dropper to apply a few drops to areas of hair loss on the scalp. Gently massage with fingertips for 3-5 minutes until fully absorbed. Using more product or applying it more frequently will not improve results. Continued use is required to help maintain hair regrowth; otherwise, hair loss may resume

Warnings

For external use only.

Do not use

On broken or irritated scalp if allergic to any ingredients if pregnant or nursing, or have any underlying medical condition - consult a healthcare provider before use

When using this product

Avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor

Top use and ask a doctor if: you experience headache, scalp redness, swelling, nausea, dizziness, or other adverse reactions.

Keep out of reach of children

: if swallowed, get medical help or contact a Poison Control Center right away.

Inactive ingredients

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

Forms and strengths

From the FDA NDC Directory · 2 product codes

Dosage formStrengthRouteNDCs
Liquid.5 g/10gtopical1
Liquid5 g/100mLtopical1

Side effect reports to FDA

FDA Adverse Event Reporting System (FAERS), 44,659 reports that list minoxidil, data through 07/30/2026

Anyone can report a problem to FDA, and a report does not mean the drug caused the problem. Reports can be duplicated or incomplete, and counts depend on how widely a drug is used. Do not stop or change a medicine because of this list. Talk to your doctor or pharmacist.

Most often reported reactions

  • Adverse drug reaction8,585
  • Drug ineffective7,760
  • Alopecia3,801
  • Application site pruritus2,926
  • Off label use2,275
  • Overdose1,461
  • Application site irritation1,420
  • Application site pain1,413
  • Hair texture abnormal1,409
  • Headache1,342

To report a side effect, use FDA MedWatch.

Manufacturers and labels

2 FDA labels

  • Guangzhou Ariel Medical Technology Co., Ltd.Shown here505G(a)(3) · Label 07/01/2026 · NDC 87815-001Full label
  • Shenzhen Deshijian Medical Equipment Co., LtdM032 · Label 06/04/2026 · NDC 85741-004Full label

Related recalls

FDA drug recalls that name this drug or its active ingredient

All drug recalls

Minoxidil Hair Growth Serum: common questions

What is Minoxidil Hair Growth Serum used for?
To regrow hair on the scalp
Is Minoxidil Hair Growth Serum a prescription drug?
No. Minoxidil Hair Growth Serum is sold over the counter (OTC) without a prescription.
Are there other products with the same active ingredient as Minoxidil Hair Growth Serum?
Yes. Other FDA-listed products with the same active ingredients include Hair Regrowth Treatment, Minoxidil (For Men), Minoxidil for Women, Minoxidil.
Who makes Minoxidil Hair Growth Serum?
2 manufacturers list Minoxidil Hair Growth Serum with the FDA, including Guangzhou Ariel Medical Technology Co., Ltd., Shenzhen Deshijian Medical Equipment Co., Ltd.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 07/01/2026 · Label text is shown as published by the manufacturer. Not medical advice