Drug labels

JOHNSON FOAM PRO

FINASTERIDE FOAM WITH 5% MINOXIDIL · JOHNSON BIOPHARMACEUTICAL INC. · TOPICAL

HUMAN OTC DRUG
Open FDA's page for this record
Set ID
27697b1c-f713-f7e0-e063-6394a90a7514
ID
581d631c-ecc9-940c-e063-6294a90aa0e1
Effective time
20260802
Version
5
SPL product data elements

JOHNSON FOAM PRO FINASTERIDE FOAM WITH 5% MINOXIDIL FINASTERIDE FINASTERIDE MINOXIDIL MINOXIDIL ALCOHOL POLOXAMER 407 ZINC PIDOLATE GLYCERIN EDETATE DISODIUM CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) BUTYLATED HYDROXYTOLUENE WATER LEVOMENTHOL UBIQUINOL POLYSORBATE 80

SPL unclassified section
JOHNSON FOAM PRO
Active ingredient
MINOXIDIL 5% FINASTERIDE 0.25%
Purpose
Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.
Indications and usage
Fight primarycause ofhalr loss in men.Antihalrlosstohelpincreasehairdenslty andvolume.
Warnings
Forexternaluse only. Foruse by men only. Extremely Flammable. Avoid fire, flame, or smoking during andimmedlately following application.
Do not use

you have no famlly hlstory of halrloss. you rhalrloss is sudden and/or patchy. you do not know the reason for your halr loss. you are under 18 years of age. Do not useonbables or chikdren. yourscalp is red, inflamed,infected,rritated, or painful. you use other medicines on the scalp.

When using

do not apply on other parts of the body. avold contact with eyes. In case ofaccldental contact.rinse eyes with large amounts ofcooltap water. some people have experienced changes in halr colorandortexture.

Stop use

chest pain, rapld heartbeat, faintness,ordlzziness occurs. sudden,unexplained weight gain occurs. your hands or feet swell. scalp irritation or redness occurs. umwanted facialhalrgrowth occurs. you donot see halrregrowthin 4 months.

Keep out of reach of children
If swallowed,getmedical help or contacta Poison Control Center right away.
Dosage and administration

1.PREP HANDSWITH COLD WATERRinse Your Fingers inCald WaterAnd Doy Them note: Foam Wll MeltOn Contat WithWarmSurfacs. 2.OPENCHILD RESISTANTCAPBe Sure To Align Arrow On The CapWith Arrow On Blue Ring.Tit capBadkAnd Pull ot. 3.DISPENSEVERTICALLYONTOACOLDSURFACEHoldThe Can Staght UpsideDown.if You Hdd ThecanAtAnAngle, Foam May Nat DispansePoperhy, PressNozzie To Dispe nseHalfACapiu OfFoam Onto CaldSuface(e gdshorCod Hands). 4.APPLYTOSCALP, NOTHAIRPart Your Hair To Expose HairLossAra. Massage Foamhno Sedp.NotHair, Repeat UnslAllHar LossAras Have Been Covered. 5.CLOSE CAP AND WASHHANDSsn ap cap back into plaoe be surearows do notline up,socapmmanschid resistant, wash hands andamysurace thoroughly a feruse .

Inactive ingredient

ALCOHOL GLYCERIN WHATER CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) UBIQUINOL ZINC PIDOLATE BUTYLATED HYDROXYTOLUENE EDETATE DISODIUM LEVOMENTHOL Poloxzam POLYSORBATE 80

Package label principal display panel
label3
Harmonized identifiers (openFDA)
Application number
505G(a)(3)
Brand name
JOHNSON FOAM PRO
Generic name
FINASTERIDE FOAM WITH 5% MINOXIDIL
Manufacturer name
JOHNSON BIOPHARMACEUTICAL INC.
Product NDC
84539-002
Product type
HUMAN OTC DRUG
Route
TOPICAL
Substance name
FINASTERIDE, MINOXIDIL
SPL ID
581d631c-ecc9-940c-e063-6294a90aa0e1
SPL set ID
27697b1c-f713-f7e0-e063-6394a90a7514
Package NDC
84539-002-01
Is original packager
true
Nui
N0000175836, N0000000126, N0000175379, N0000175564
Pharm class epc
5-alpha Reductase Inhibitor [EPC], Arteriolar Vasodilator [EPC]
Pharm class moa
5-alpha Reductase Inhibitors [MoA]
Pharm class pe
Arteriolar Vasodilation [PE]
UNII
57GNO57U7G, 5965120SH1
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.