5% Minoxidil Sprays HAIR EGROWTH TREATMENT

MINOXIDIL 5% TOPICAL HUMAN OTC DRUG

5% Minoxidil Sprays HAIR EGROWTH TREATMENT is an FDA drug label for the active ingredient MINOXIDIL 5% manufactured by Tuosen Hong Kong Import Export Trading Co., Limited administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260727.

Generic name
MINOXIDIL 5%
Manufacturer
Tuosen Hong Kong Import Export Trading Co., Limited
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87880-001
Application
505G(a)(3)
Label effective
20260727

About this product

5% Minoxidil Sprays HAIR EGROWTH TREATMENT is an FDA-registered drug product whose active ingredient is MINOXIDIL 5%. It is labelled by Tuosen Hong Kong Import Export Trading Co., Limited taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87880-001, application 505G(a)(3), label effective 20260727. It is one of 3 FDA drug label records sharing the active ingredient MINOXIDIL 5%. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing MINOXIDIL 5% are most often described in connection with: regrow hair. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Minoxidil 5%

Indications & Usage

Use to regrow hair on the scalp

Dosage & Administration

apply one ml twice a day directly onto the scalp in the hair loss area for men Using more or more often will not improve results apply one ml twice a day directly onto the scalp in the hair loss area for women Continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again

Warnings

For external use only

More products with the same ingredient

MINOXIDIL 5%

5% Minoxidil Hair Growth Serum Roll-on

Shenzhen Boyimei Technology Co., Ltd. View label

MDhair Extra Strength hair regrowth treatment for Men

MDalgorithms, Inc View label

How products containing MINOXIDIL 5% compare

FDA lists 3 drug label records with MINOXIDIL 5% as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — MDalgorithms, Inc 1
— — Shenzhen Boyimei Technology Co., Ltd. 1
— — Tuosen Hong Kong Import Export Trading Co., Limited 1
— — — —
— — — —

Frequently asked questions

What is 5% Minoxidil Sprays HAIR EGROWTH TREATMENT used for?
Use to regrow hair on the scalp

Who makes 5% Minoxidil Sprays HAIR EGROWTH TREATMENT?
Tuosen Hong Kong Import Export Trading Co., Limited is the labeler of record for 5% Minoxidil Sprays HAIR EGROWTH TREATMENT. 3 FDA label records share the active ingredient MINOXIDIL 5%, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does 5% Minoxidil Sprays HAIR EGROWTH TREATMENT come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is 5% Minoxidil Sprays HAIR EGROWTH TREATMENT prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing MINOXIDIL 5%?
Yes. 3 FDA drug label records list MINOXIDIL 5% as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has 5% Minoxidil Sprays HAIR EGROWTH TREATMENT been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.