Minoxidil Topical Solution
Minoxidil Topical Solution is an FDA drug label for the active ingredient MINOXIDIL TOPICAL SOLUTION manufactured by Growth Essence LLC 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 20260515.
- Generic name
- MINOXIDIL TOPICAL SOLUTION
- Manufacturer
- Growth Essence LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87399-002
- Application
- 505G(a)(3)
- Label effective
- 20260515
About this product
Minoxidil Topical Solution is an FDA-registered drug product whose active ingredient is MINOXIDIL TOPICAL SOLUTION. It is labelled by Growth Essence LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87399-002, application 505G(a)(3), label effective 20260515. 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 TOPICAL SOLUTION are most often described in connection with: regrows hair, scalp vertex. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use Uses Regrows hair on the top of the scalp, (vertex only).
Dosage & Administration
Directions 1. Wet hair and scalp thoroughly. 2. Apply shampoo to the top of the scalp only. 3. Massage gently until a lather forms. 4. Leave on the scalp for 2-3 minutes. 5. Rinse thoroughly.
Warnings
Warnings For external use only.
Frequently asked questions
What is Minoxidil Topical Solution used for?
Use Uses Regrows hair on the top of the scalp, (vertex only).
Who makes Minoxidil Topical Solution?
Growth Essence LLC is the labeler of record for Minoxidil Topical Solution.
What form does Minoxidil Topical Solution 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 Minoxidil Topical Solution 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.
Has Minoxidil Topical Solution 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.