Label: GEMBOOXT KETOCONAZOLE 1% MEDICATED SHAMPOOS- ketoconazole liquid

  • NDC Code(s): 76986-025-01, 76986-025-02, 76986-025-03
  • Packager: Guangdong Quadrant Ecological Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 30, 2026

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  • ACTIVE INGREDIENT

    Ketoconazole 1%

  • PURPOSE

    Anti-dandruff shampoo

  • INDICATIONS & USAGE

    Controls flaking, scaling and itching associated with dandruff

  • WARNINGS

    For external use only.

  • DO NOT USE


    on scalp that is broken or inflamed.
    if you are allergic to ingredients in this product.

  • WHEN USING

    When using this products. Avoid contact with eyes. lf contact occurs, rinse thoroughly with water.
    If pregnant or breast-feeding, ask a doctor before use.

  • STOP USE

    rash appears.
    condition worsens or does not improve in 2-4 weeks.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION


    For adults and children 12 years and older:
    1. Wet hair thoroughly.
    2. Apply shampoo, generously lather, rinse thoroughly. Repeat.
    3. Use every 3-4 days for up to 8 weeks or as directed by a doctor.Then use only as needed to control dandruff.
    Children under 12 years: Ask a doctor.

  • INACTIVE INGREDIENT

    WATER
    SODIUM LAUROYL SARCOSINATE
    COCAMIDOPROPYL BETAINE
    WATER
    PARFUM
    GLYCERYL CAPRYLATE
    GLYCERYL LAURATE
    PHENOXYETHANOL
    WATER
    LAURYL LACTATE
    CITRIC ACID
    POLYQUATERNIUM-10
    DISODIUM EDTA
    HYDROLYZED RHODOPHYCEAE EXTRACT
    BUTYLENE GLYCOL
    1,2-HEXANEDIOL
    PENTYLENE GLYCOL
    PROPANEDIOL
    CAPRYLHYDROXAMIC ACID
    ETHYLHEXYLGLYCERIN
    BIOTIN
    POTASSIUM HYDROXIDE

  • PRINCIPAL DISPLAY PANEL

    label2

  • INGREDIENTS AND APPEARANCE
    GEMBOOXT KETOCONAZOLE 1% MEDICATED SHAMPOOS 
    ketoconazole liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76986-025
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE0.01 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURYL LACTATE (UNII: G5SU0BFK7O)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
    WATER (UNII: 059QF0KO0R)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    BIOTIN (UNII: 6SO6U10H04)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    GLYCERYL LAURATE (UNII: Y98611C087)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76986-025-01300 mL in 1 BOTTLE; Type 0: Not a Combination Product01/30/2026
    2NDC:76986-025-02450 mL in 1 BOTTLE; Type 0: Not a Combination Product01/30/2026
    3NDC:76986-025-03750 mL in 1 BOTTLE; Type 0: Not a Combination Product01/30/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/30/2026
    Labeler - Guangdong Quadrant Ecological Technology Co., Ltd. (554532634)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Quadrant Ecological Technology Co., Ltd.554532634manufacture(76986-025)
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