JOHNSON FOAM PRO
JOHNSON FOAM PRO is an FDA drug label for the active ingredient FINASTERIDE FOAM WITH 5% MINOXIDIL manufactured by JOHNSON BIOPHARMACEUTICAL INC. 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 20260802.
- Generic name
- FINASTERIDE FOAM WITH 5% MINOXIDIL
- Manufacturer
- JOHNSON BIOPHARMACEUTICAL INC.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 84539-002
- Application
- 505G(a)(3)
- Label effective
- 20260802
About this product
JOHNSON FOAM PRO is an FDA-registered drug product whose active ingredient is FINASTERIDE FOAM WITH 5% MINOXIDIL. It is labelled by JOHNSON BIOPHARMACEUTICAL INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84539-002, application 505G(a)(3), label effective 20260802. 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 FINASTERIDE FOAM WITH 5% MINOXIDIL are most often described in connection with: fight primarycause, ofhalr loss, men antihalrlosstohelpincreasehairdenslty. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.
Dosage & Administration
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Warnings
Forexternaluse only. Foruse by men only. Extremely Flammable. Avoid fire, flame, or smoking during andimmedlately following application.
Frequently asked questions
What is JOHNSON FOAM PRO used for?
Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.
Who makes JOHNSON FOAM PRO?
JOHNSON BIOPHARMACEUTICAL INC. is the labeler of record for JOHNSON FOAM PRO.
What form does JOHNSON FOAM PRO 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 JOHNSON FOAM PRO 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 JOHNSON FOAM PRO 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.