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
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated May 10, 2024

If you are a consumer or patient 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
    ANDAANDA07535705/10/2024
    Labeler - Good Manager Holdings Inc (118382673)
    Establishment
    NameAddressID/FEIBusiness Operations
    Good Manager Holdings Inc118382673manufacture(82372-011)