Label: MINOXIDIL HAIR GROWTH SPRAYS- minoxidil 5% liquid

  • NDC Code(s): 83788-201-01
  • Packager: Xiamen Panmai Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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  • SPL UNCLASSIFIED SECTION

    Minoxidil Hair Growth Spray

  • ACTIVE INGREDIENT

    Minoxidil 5%

  • PURPOSE

    HAIR REGROW THTREATMENT

  • INDICATIONS & USAGE

    Stimubtes Natural Hair Growth
    Strouger, Thicker, Fuller Hair
    Treat Oameged Hair

  • WARNINGS

    Don't use if you are:PregnanL
    Feeding.
    Haring heart gergiolity
    Super-8engitie skin
    Haing open wounds
    Planning to do ahysical ac vitigs in the meat hour.

  • DO NOT USE

    Don't use if you are:PregnanL
    Feeding.
    Haring heart gergiolity
    Super-8engitie skin
    Haing open wounds
    Planning to do ahysical ac vitigs in the meat hour.

  • WHEN USING

    STEP 1
    FOR SCALP : Direct jet the scalp with six sprays from the back to the crown to the frontal region.FOR BEARD : Direct-jet each cheek with two sprays.
    STEP 2
    Use twice daily on clean hair. Use fingertips to massage the solution intoskin/hair for 2-3 minutes(Apply pressure, so thatblood flow can increase for both scalp and beard)

  • STOP USE

    If there are adverse reactions such as itching and redness, please stop using immediately and seek medical help.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Use twice daily on clean hair. Use fingertips to massage the solution intoskin/hair for 2-3 minutes(Apply pressure, so thatblood flow can increase for both scalp and beard)

  • STORAGE AND HANDLING

    store at room temperature

  • INACTIVE INGREDIENT

    Aqua
    Propylene Glycol
    Glycerin

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MINOXIDIL HAIR GROWTH SPRAYS 
    minoxidil 5% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83788-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83788-201-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product11/08/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03211/08/2023
    Labeler - Xiamen Panmai Technology Co., Ltd (416680201)
    Establishment
    NameAddressID/FEIBusiness Operations
    Xiamen Panmai Technology Co., Ltd416680201manufacture(83788-201)
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