Label: MENS PURA DOR HAIR LOSS MD- minoxidil 5% solution

  • NDC Code(s): 69019-001-01
  • Packager: Vitals International Group
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated January 18, 2023

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

  • ACTIVE INGREDIENT

    Minoxidil 5% w/v

  • PURPOSE

    Hair regrowth treatment for men

  • USE

    Use to regrow hair on the top of the scalp (vertex only, see pictures on side of carton)

  • WARNINGS

    For external use only. For use by men only.

    Flammable: Keep away from fire or flame

  • DO NOT USE

    Do not use if: • you are a woman • your amount of hair loss is different than that shown

    on the side of this carton or your hair loss is on the front of the scalp, 5% minoxidil topical

    solution is not intended for frontal baldness or receding hairline

    • you have no family history of hair loss • your hair loss is sudden and/or patchy

    • you do not know the reason for your hair loss • you are under 18 years of age. Do not

    use on babies and children • your scalp is red, inflamed, irritated or painful • you use

    other medicines on the scalp

  • ASK DOCTOR

    Ask a doctor before use if you have heart disease

  • 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 men, 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 person. This product will not

    work for all men.

  • STOP USE

    Stop use and ask a doctor if

    • chest pain, rapid heartbeat, faintness, or dizziness occurs

    • 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

  • PREGNANCY OR BREAST FEEDING

    May be harmful if used when pregnant or breast-feeding.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    Directions • apply one mL with dropper 2 times a day 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 keep your hair regrowth, or hair loss will begin again

  • OTHER SAFETY INFORMATION

    Other information • see hair loss pictures on side of this carton

    • before use, read all information on carton and enclosed leaflet • keep the carton. It

    contains important information. • hair regrowth has not been shown to last longer than

    48 weeks in large clinical trials with continuous treatment with 5% minoxidil topical

    solution for men • in clinical studies of mostly white men aged 18-49 years with

    moderate degrees of hair loss, 5% minoxidil topical solution for men provided more hair

    regrowth than 2% minoxidil topical solution

    • store at controlled room temperature 20º to 25ºC (68º to 77ºF).

  • INACTIVE INGREDIENT

    Alcohol, Propylene Glycol, Purified Water

  • QUESTIONS

    Questions or comments? 855-PURADOR

    • Visit Website at www.purador.com

  • PRINCIPAL DISPLAY PANEL

    Box

  • INGREDIENTS AND APPEARANCE
    MENS PURA DOR HAIR LOSS MD 
    minoxidil 5% solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69019-001
    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
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69019-001-011 in 1 BOX09/27/2019
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07623909/27/2019
    Labeler - Vitals International Group (049656991)