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Minoxidil (For Men)

minoxidil · Minoxidil (For Men) is an arteriolar vasodilator (over-the-counter) containing minoxidil, made by 9 manufacturers.

Type
Over the counter
Drug class
Arteriolar Vasodilator
Route
Topical
Manufacturers
9

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Drug facts

Generic name
minoxidil
Active ingredients
Minoxidil
Dosage forms
Aerosol, foam, Liquid
Label holder
FlexiGo Inc
FDA application
ANDA218616
Label updated
06/04/2026

Active ingredients

OTC-ACTIVE INGREDIENT SECTION

Purpose

OTC-PURPOSE SECTION

Uses

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Directions

&ADMINISTRATION SECTION

Warnings

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Do not use

OTC-DO NOT USE SECTION

Ask a doctor before use

OTC-ASK DOCTOR SECTION

When using this product

OTC-WHEN USING SECTION

Stop use and ask a doctor

OTC-STOP USE SECTION

Keep out of reach of children

OTC-KEEP OUT OF REACH OF CHILDREN SECTION

Inactive ingredients

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Forms and strengths

From the FDA NDC Directory · 9 product codes

Dosage formStrengthRouteNDCs
Aerosol, foam50 mg/gtopical8
Liquid5 g/100gtopical1

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

9 FDA labels

  • FlexiGo IncShown hereANDA218616 · Label 06/04/2026 · NDC 85524-2611Full label
  • BosleyMDANDA208092 · Label 03/24/2026 · NDC 69113-501Full label
  • CARDINAL HEALTH 110, LLC. DBA LEADERANDA218616 · Label 04/13/2026 · NDC 70000-0754Full label
  • CVS PharmacyANDA209074 · Label 04/06/2026 · NDC 51316-212Full label
  • RESTORATION HOLDINGS, LLCANDA209074 · Label 12/11/2024 · NDC 82796-100Full label
  • SCIENTIFIC HAIR RESEARCH, LLCANDA209074 · Label 07/03/2024 · NDC 69113-128Full label
  • SPAZI INC.ANDA209074 · Label 01/23/2024 · NDC 82376-6006Full label
  • TARGET CorporationANDA209074 · Label 05/17/2024 · NDC 11673-157Full label
  • Walgreen CompanyANDA209074 · Label 10/10/2022 · NDC 0363-9090Full label

Related recalls

FDA drug recalls that name this drug or its active ingredient

All drug recalls

Minoxidil (For Men): common questions

What is Minoxidil (For Men) used for?
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Is Minoxidil (For Men) a prescription drug?
No. Minoxidil (For Men) is sold over the counter (OTC) without a prescription.
Are there other products with the same active ingredient as Minoxidil (For Men)?
Yes. Other FDA-listed products with the same active ingredients include Hair Regrowth Treatment, Minoxidil for Women, Minoxidil, Minoxidil 5% (For Men).
Who makes Minoxidil (For Men)?
9 manufacturers list Minoxidil (For Men) with the FDA, including FlexiGo Inc, BosleyMD, CARDINAL HEALTH 110, LLC. DBA LEADER.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 06/04/2026 · Label text is shown as published by the manufacturer. Not medical advice