Label: ANTI DANDRUFF- ketoconazole liquid

  • NDC Code(s): 74458-157-01
  • Packager: Guangzhou Yilong Cosmetics.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 4, 2026

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

  • KEEP OUT OF REACH OF CHILDREN

    STORAGE
    Store at room temperature away frommoisture and direct sunlight.
    Keep the bottle tightlyclosed.
    Keep out of reach of children and pets.

  • INDICATIONS & USAGE

    DIRECTIONS FOR USE
    For best results, follow these stepscarefully:
    1.Wet hair and scalp thoroughly with
    lukewarm water.
    2.Applya sufficient amountof shampoo to
    generate a rich lather.
    3.Gently massage the lather into your scalp
    and hair.
    4.Leave the lather on the scalpfor3-5minutes. This contact time is crucialforthemedication to work effectively.5.Rinse thoroughly with water.

  • WARNINGS

    PRECAUTIONS
    For externaluse only.Avoid contact witheyes. Ifcontactoccurs, rinse thoroughlywithwater.Stop use and consult a doctor if youexperience severe irritation, rash, oranysigns of an allergic reaction (e.g., swelling,dizziness, trouble breathing). Before usingthis shampoo if you have known allergiesto ketoconazole or any other ingredients.

  • INACTIVE INGREDIENT

    Aqua
    Sodium Laureth Sulfate
    Cocamide DEA
    Sodium Chloride
    Cocamidopropyl Betaine
    Ammonium Lauryl Sulfate
    Fragrance
    Phenoxyethanol
    PEG-7 Glyceryl Cocoate
    Bis-Aminopropyl Dimethicone
    Hydroxypropyl Guar
    Hydroxypropyltrimonium Chloride
    C12-13 Pareth Lactate
    Citric Acid
    C11-15 Pareth-9
    Trideceth-12
    Sodium Benzoate

  • PURPOSE

    Ketoconazole 1% w/w....Anti-dandruff shampoo

  • DOSAGE & ADMINISTRATION

    Use every 3-4 days for up to 8 weeks. Afterthat, use only as needed to control dandruff.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    ANTI DANDRUFF 
    ketoconazole liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74458-157
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE1 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    AQUA (UNII: 059QF0KO0R) 50 mg  in 100 mg
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74458-157-01200 mg in 1 BOTTLE; Type 0: Not a Combination Product07/04/2026
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03207/04/2026
    Labeler - Guangzhou Yilong Cosmetics.,Ltd (420929116)
    Registrant - Guangzhou Yilong Cosmetics.,Ltd (420929116)