Label: MINOXIDIL HAIR GENERATION SERUM- 5% minoxidil with biotin paste

  • NDC Code(s): 85593-020-01
  • Packager: Guangzhou ChuanMa International Trading Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2025

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredients:Minoxidil (5%),Finasteride(0.1%)

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of childrerIf swallowed, get medical help orcontact a Poison Control Centerright away.

  • PURPOSE

    Purpose:Fight primary cause of hair loss inmen. Anti-hair loss to helpincrease hair density and volume.

  • WARNINGS

    Warnings:
    for external use only.for use by men only.extremelyflammable.avoid fire, flame, or smoking duringand immediately following application.

  • INDICATIONS & USAGE

    1. PREP HANDS WITH
    COLD WATER
    Rinse your fingers in cold
    water and dry them.
    Note: Foam will melt on
    contact with warm surfaces
    2.OPEN THE CAP
    Tilt cap back and pull off.
    3.DISPENSE VERTICALLY
    ONTO A COLD SURFACE
    Press nozzle to dispense half acapful of foam onto cold
    surface(e.g.dish.or cold hands)
    4.APPLY TO SCALP, NOT HAIR
    Part your hair to expose hair lossarea.Massage foam into scalp, notHair, repeat until all hair loss areashave been covered.
    5.CLOSE CAP AND
    WASH HANDS
    Snap cap back into place,
    wash hands and any surface
    thoroughly after use.

  • DOSAGE & ADMINISTRATION

    Take an appropriate amount and place it in the palm

  • INACTIVE INGREDIENT

    Butanediol, Water, Ethanol, Menthol.Pca Zinc, Sodium LaurethCarboxylate, Ppg-10 Sorbitol,Sodium Cocoyl Glycinate, DisodiumCocoyl Glutamate, Sodium Chloride,Cocoamidopropyl Betaine,Panthenol, DimethylsilanolHyaluronic Acid, Poloxamer 407

  • PRINCIPAL DISPLAY PANEL

    labeling

  • INGREDIENTS AND APPEARANCE
    MINOXIDIL HAIR GENERATION SERUM 
    5% minoxidil with biotin paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85593-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G) FINASTERIDE0.1 g  in 100 g
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    1,4-BUTANEDIOL (UNII: 7XOO2LE6G3)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ZINC PCA (UNII: C32PQ86DH4)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    MENTHOL, (+)- (UNII: C6B1OE8P3W)  
    SODIUM LAURETH-5 CARBOXYLATE (UNII: 5PJ5L1DC1U)  
    SODIUM COCOYL GLYCINATE (UNII: XLU9KH03XM)  
    DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)  
    SORBITOL (UNII: 506T60A25R)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85593-020-0190 g in 1 BOTTLE; Type 0: Not a Combination Product12/16/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/16/2025
    Labeler - Guangzhou ChuanMa International Trading Co.,Ltd. (510247477)
    Registrant - Guangzhou ChuanMa International Trading Co.,Ltd. (510247477)