Label: 5% MINOXIDIL HAIR REGROWTH SERUM WITH BIOTIN- minoxidil liquid

  • NDC Code(s): 87394-001-01, 87394-001-02
  • Packager: Shenzhen Huayuan Hengsheng Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 2, 2026

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  • ACTIVE INGREDIENT

    Minoxidil 5%

  • PURPOSE

    Hair Regrowth

  • INDICATIONS & USAGE

    to help regrow hair on the scalp

  • WARNINGS

    For external use only

  • DO NOT USE


    if you are under 18 years of age
    on other parts of the body,Use only on scalp

  • WHEN USING


    Ask a doctor before use if you have
    heart disease.
    hign bolld pressure.
    sudden.patchy.or unexplained hair loss
    a sensitive,imtated,or sunburned scalp.
    Ask a doctor or pharmacist before use if you are
    taking any prescription medications ofr high blood pressure
    When using this product
    avoid contact with eyes,lf comtact occurs.rinse thoroughly with cool water.
    do not apply to broken skin.

  • STOP USE


    Chest pain,rapid heartbeat.faintness.or dizziness occurs.
    Sudden unexplained weight gain occurs.
    Scalp redness or irritation occurs.
    Unwanted facial hair growth occurs.

  • KEEP OUT OF REACH OF CHILDREN

    if swallowed.get mediacl help or contact a poison control Center right away(1-800-222-1222)

  • DOSAGE & ADMINISTRATION


    Apply 1 mL of solution to the dry scalp in the hair loss area twice daily (morning and night).
    Apply with fingers
    wash hands thoroughly after application

  • INACTIVE INGREDIENT

    Alcohol,biotin,Butylene Glycol ,Glycerin,panthenol water

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    5% MINOXIDIL HAIR REGROWTH SERUM WITH BIOTIN 
    minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87394-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    BIOTIN (UNII: 6SO6U10H04)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87394-001-012 in 1 BOX02/03/2026
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:87394-001-022 in 1 PACKAGE02/03/2026
    22 in 1 BOX
    260 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/03/2026
    Labeler - Shenzhen Huayuan Hengsheng Technology Co., Ltd. (570254468)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Huayuan Hengsheng Technology Co., Ltd.570254468manufacture(87394-001)
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