JOHNSON FOAM

JOHNSON FOAM is an FDA-registered drug product whose active ingredient is MINOXIDIL. It is labelled by JOHNSON BIOPHARMACEUTICAL INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84539-001, application M032, label effective 20260802. It is one of 90 FDA drug label records sharing the active ingredient MINOXIDIL. 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.

Across FDA labelling, products containing MINOXIDIL are most often described in connection with: fight primary, cause hair, loss men, lossto help, body avoid, contactwith eyes, case accidental, large amounts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Fight primary cause of hair loss in men.Anti hair lossto help increase hair density and volume do not apply on other parts of the body. avoid contactwith eyes.In case of accidental contactrinse eyes with large amounts of cool tap water. some people have experienced changes in hair colorand/or texture

1.PREP HANDSWITH COLD WATERRinse Your Fingers In Cold WaterAnd DryThem.note:Foam Will MeltOn Contact With Warm Surfaces. 2.OPEN CHILDRESISTANT CAP Be Sure To Align Arrow On The capWith Arrow On Blue Ring. Tilt CapBack And Pull Off. 3.DISPENSEVERTICALLYONTOACOLD SURFACE Hold The Can Straight UpsideDown.lf You Hold Thecan At AnAngle, Foam May Not DispenseProperly.Press Nozzle To DispenseHalfACapful Of Foam Onto ColdSurface(e.g.dish.or Cold Hands). 4.APPLYTOSCALP.NOT HAIR Part Your Hair To Expose Hair LossArea.Massage Foam Into ScalpNot Hair, Repeat UntilAll HairLossAreas Have Been Covered. 5.CLOSE CAP AND WASHHANDSsnap cap back into place be surearrows do not line up, so cap remainschild resistant, wash hands and anysurface thoroughly afteruse

For external use only For use by men only. Extremely Flammable Avoid fire, flame, or smoking during and immediatelyfollowing application.

FDA lists 90 drug label records with MINOXIDIL 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.

What is JOHNSON FOAM used for?
Fight primary cause of hair loss in men.Anti hair lossto help increase hair density and volume do not apply on other parts of the body. avoid contactwith eyes.In case of accidental contactrinse eyes with large amounts of cool tap water. some people have experienced changes in hair colorand/or texture

Who makes JOHNSON FOAM?
JOHNSON BIOPHARMACEUTICAL INC. is the labeler of record for JOHNSON FOAM. 90 FDA label records share the active ingredient MINOXIDIL, 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 JOHNSON FOAM 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 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?
Yes. 90 FDA drug label records list MINOXIDIL 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 JOHNSON FOAM 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.