Label: JOHNSON FOAM FOR MEN- minoxidil aerosol, foam
- NDC Code(s): 84539-001-01
- Packager: JOHNSON BIOPHARMACEUTICAL INC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 15, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
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 - WARNINGS
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DOSAGE & ADMINISTRATION
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
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
JOHNSON FOAM FOR MEN
minoxidil aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84539-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G) FINASTERIDE 0.1 g in 100 g MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) COCODIMONIUM HYDROXYPROPYL HYDROLYZED KERATIN (1000 MW) (UNII: 8V0I3U3HMO) UBIQUINOL (UNII: M9NL0C577Y) BIOTIN (UNII: 6SO6U10H04) ZINC PIDOLATE (UNII: C32PQ86DH4) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) LEVOMENTHOL (UNII: BZ1R15MTK7) POLOXAMER 407 (UNII: TUF2IVW3M2) POLYSORBATE 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84539-001-01 90 g in 1 BOTTLE; Type 0: Not a Combination Product 07/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 07/15/2024 Labeler - JOHNSON BIOPHARMACEUTICAL INC. (132195896) Establishment Name Address ID/FEI Business Operations JOHNSON BIOPHARMACEUTICAL INC. 132195896 manufacture(84539-001)
