Label: BLOOSKIM ANTI DANDRUFF- ketoconazole shampoo

  • NDC Code(s): 82372-013-01
  • Packager: Good Manager Holdings Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2024

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

  • ACTIVE INGREDIENT

    ketoconazole 1%

  • PURPOSE

    ANTI-DANDRUFF SHAMPOO

  • INDICATIONS & USAGE

    Controls flaking, scaling, and itching caused by dandruff

  • WHEN USING

    When using this product

    Avoid contact with eyes

    If contact occurs, rinse thoroughly with water.

  • WARNINGS

    For external use only

  • DO NOT USE

    Do not use

    On scalp that is broken or inflamed

    If you are allergic to ingredients in this product

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • STOP USE

    Stop use and ask a doctor if

    A rash appears.

    Condition worsens or does not improve within 2-4 weeks.

    If pregnant or breast-feeding, consult a doctor before use.

  • DOSAGE & ADMINISTRATION

    Directions

    adults and children 12 years and over

    Wet hair thoroughly.

    Apply shampoo, lather generously, and rinse thoroughly.

    Repeat if necessary.

    Use every 3-4 days for up to 8 weeks or as directed by a doctor.

    Afterward, use as needed to control dandruff.

    children under 12 years

    Ask a doctor

  • OTHER SAFETY INFORMATION

    Store at 20°C to 25°C (68°F to 77°F)

  • INACTIVE INGREDIENT

    Citric Acid, Herba Violae, Euphorbia Hirta, Murraya Paniculata , Mentha Canadensis, Sophora Flavescens, Dittany Bark, Glabrous Greenbrier Rhizome, Mosla Cavaleriei Levl, Stellera Chamaejasme, Huang Bai, Sessile Stemona Root, Gleditsia Sinensis, Common Cnidium Fruit, Fructus Kochiae, Tea Tree Oil, Water

  • PRINCIPAL DISPLAY PANEL

    anti dandruff

  • INGREDIENTS AND APPEARANCE
    BLOOSKIM ANTI DANDRUFF 
    ketoconazole shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82372-013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    MURRAYA PANICULATA WHOLE (UNII: Y8ZAA3Z7WU)  
    MENTHA CANADENSIS WHOLE (UNII: J1BO4MHT2L)  
    GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)  
    WATER (UNII: 059QF0KO0R)  
    SMILAX GLABRA TUBER (UNII: PES3YXA3LR)  
    MOSLA CAVALERIEI WHOLE (UNII: 05O8B64OS2)  
    VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54)  
    EUPHORBIA HIRTA (UNII: L13YF113GN)  
    DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)  
    SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)  
    PHELLODENDRON CHINENSE WHOLE (UNII: QKA3ZK8IIE)  
    STEMONA SESSILIFOLIA ROOT (UNII: EKG8030U4N)  
    BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82372-013-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product11/08/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00511/08/2024
    Labeler - Good Manager Holdings Inc (118382673)