Label: DIZOP 5% MINOXIDIL TOPICAL GEL- minoxidil gel

  • NDC Code(s): 83766-102-01, 83766-102-02
  • Packager: Shenzhen Joyuflsh Technology Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 9, 2024

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

  • SPL UNCLASSIFIED SECTION

    DIZOP 5% Minoxidil Topical Gel

  • ACTIVE INGREDIENT

    Minoxidil 5%

  • PURPOSE

    Hair regrowth treatment

  • INDICATIONS & USAGE

    Apply 3-4 drops of Minoxidil Gel directly to the scalp in the area to be treated.
    Massage into the scalp with your fingers then wash hands thoroughly.
    Using more or using more often will not improve results; continued use is necessary to promote and maintain hair regrowth.

  • WARNINGS

    For external use only.

  • DO NOT USE

    Your amount of hair loss is different than that shown the side of this carton or your hair loss is on the front of the scalp. 5% Minoxidil Gel is not intended for frontal baldness or receding hairline.
    you have no family history of hair loss.
    your hair loss is sudden and/or patch.
    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, infected, irritated, or painful.
    you use other medicines on the scalp.

  • WHEN USING

    Do not apply on other parts of the body. Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water. lt takes time to regrow hair. You may need to use this product 1 times a day for at least 3 months before you see results, The amount of hair regrowth is different for each person.The product will not work for everyone.

  • STOP USE

    lf scalp irritation or redness occurs. lf you get unwanted facial hair growth. lf you do not see hair regrowth in 4 months.lf sudden, unexplained weight gain occurs.

  • KEEP OUT OF REACH OF CHILDREN

    lf swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222

  • DOSAGE & ADMINISTRATION

    Apply 3-4 drops of Minoxidil Gel directly to the scalp in the area to be treated.

    Massage into the scalp with your fingers then wash hands thoroughly.

    Using more or using more often will not improve results; continued use is necessary to promote and maintain hair regrowth.

  • STORAGE AND HANDLING

    Before use, read all information on the carton.
    Keep the carton. It contains important information.
    Store at a controlled room temperature of 5 to 30 C (41 to 86°F).
    Kindly ensure the lid remains closed. Do not store at temperatures above 40C(104°F).

  • INACTIVE INGREDIENT

    Minoxidil
    ALCOHOL
    GLYCERIN
    CETYL ALCOHOL
    MYRISTYL LACTATE
    POLYSORBATE 60
    SODIUM THIOSULFATE
    CARBOMER HOMOPOLYMER
    TROLAMINE
    WATER

  • PRINCIPAL DISPLAY PANEL

    label1label2

  • INGREDIENTS AND APPEARANCE
    DIZOP 5% MINOXIDIL TOPICAL GEL 
    minoxidil gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83766-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SODIUM THIOSULFATE (UNII: HX1032V43M)  
    MYRISTYL LACTATE (UNII: 1D822OC34X)  
    ALCOHOL (UNII: 3K9958V90M)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83766-102-012 in 1 PACKAGE01/17/2024
    160 g in 1 CANISTER; Type 1: Convenience Kit of Co-Package
    2NDC:83766-102-023 in 1 PACKAGE01/17/2024
    260 g in 1 CANISTER; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03201/17/2024
    Labeler - Shenzhen Joyuflsh Technology Co.,Ltd. (603012375)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Joyuflsh Technology Co.,Ltd.603012375manufacture(83766-102)