Label: DAVV 2%MINOXIDIL TOPICAL SOLUTION WOMENS HAIR REGROWTH TREATMENT- hair loss product liquid

  • NDC Code(s): 82372-011-01
  • Packager: Good Manager Holdings Inc
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 25, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Minoxidil 2%

  • ASK DOCTOR

    Ask a doctor before use if you have heart disease

  • DO NOT USE

    Do not use if
    • Your hair loss occurs at the front of the scalp.
    • Minoxidit topical solution 2% is not intended for treating frontal baldness or a receding hairline.
    • There is a family history of hair loss.
    • Your hair loss is sudden or appears in patches.
    • The cause of your hair loss is unknown.
    • You are under 18 years of age. Do not use it on infants or children.
    • Your scalp is red, inflamed, infected, irritated, or painful.
    • Other medications are applied to the scalp.

  • KEEP OUT OF REACH OF CHILDREN

    May be harmful if used when pregnant or breast-feeding.
    Keep out of reach of children and pets. If swallowed, get medical help, or contact a Poison Control Center right away.

  • PURPOSE

    Hair Regrowth Treatment for Women

  • WHEN USING

    when using this product
    • do not apply on other parts of the body
    • avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water
    • some people have experienced changes in hair color and/or texture
    • it takes time to regrow hair. Results may occur at 2 months with twice a day usage. For some people, you may need to use this product for at least 4 months before you see results.
    • the amount of hair regrowth is different for each people. This product will not work for all people.

  • STOP USE

    Stop use and ask a doctor if
    • chest pain, rapid heartbeat, faintness, or dizziness.occur sudden, unexplained weight gain occurs
    • your hands or feet swell - scalp irritation or redness occurs

    • unwanted facial hair growth occurs - you do not see hair regrowth in 4 months

  • WARNINGS

    Warnings
    For external use only.

  • DOSAGE & ADMINISTRATION

    Direction
    • apply one mL with dropper 2 times a days
    directly onto the scalp in the hair loss area
    • using more or more often will not improve results
    • continued use is necessary to increase and keen our hair regrowth or hair loss will begin again

  • INACTIVE INGREDIENT

  • INACTIVE INGREDIENT

    WATER, GLYCERIN, BUTYLENE GLYCOL, PANTHENOL, TRIPEPTIDE-1, AZELAIC ACID, NIACINAMIDE, MENTHA ARVENSIS LEAF EXTRACT, HYDRANGEA MACROPHYLLA LEAF EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, PORTULACA OLERACEA EXTRACT, CHRYSANTHELLUM INDICUM EXTRACT, SOPHORA ANGUSTIFOLIA ROOT A EXTRACT, CENTELLA ASIATICA ROOT EXTRACT, CURCUMIN, HYDROLYZED WHEAT PROTEIN, MOROCCAN NUT OIL, ROSA CANINA FRUIT OIL, SODIUM HYALURONATE, BIOTIN, RETINOL, HYDROXYACETOPHENONE, 1,2-HEXANEDIOL, DISODIUM EDTA.

  • INDICATIONS & USAGE

    Use to regrow hair on the top of the scalp(vertex only)

  • PRINCIPAL DISPLAY PANEL

    Package

  • INGREDIENTS AND APPEARANCE
    DAVV 2%MINOXIDIL TOPICAL SOLUTION WOMENS HAIR REGROWTH TREATMENT 
    hair loss product liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82372-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PANTHENOL (UNII: WV9CM0O67Z)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82372-011-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product05/10/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/10/2024
    Labeler - Good Manager Holdings Inc (118382673)
    Establishment
    NameAddressID/FEIBusiness Operations
    Good Manager Holdings Inc118382673manufacture(82372-011)