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Cardinal Health Sanitizer (Cardinal Health)

Available Formats

Dosage Form Package Information Links
AEROSOL, FOAM 12 BOTTLE, SPRAY in 1 CASE (63517-523-15) > 425000 mg in 1 BOTTLE, SPRAY Label Information

Complete Cardinal Health Sanitizer Information

  • PRINCIPAL DISPLAY PANEL

    Cardinal Health Aerosol Foam Sanitizer

  • INDICATIONS & USAGE

    Directions
    • Place enough product in your palm to thoroughly cover your hands
    • Rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product

  • DOSAGE & ADMINISTRATION

    Apply approx. 3g


  • PURPOSE

    Antimicrobial


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.


  • WARNINGS

    Warnings Flam mable.
    Keep away from fire or flame.
    For external use only When using this product
    do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
    Stop use and ask a doctor if
    irritation or rash appears and lasts
    Keep out of reach of children.
    If swallowed, get medical help or contact a Poison Control Center right away.
    Contents under pressure.
    Do not puncture or incinerate container. Do not store at temperature above 120°F (48°C).
  • ACTIVE INGREDIENT

    Active ingredient Ethyl alcohol 62.5%
  • INACTIVE INGREDIENT

    Inactive Ingredients Water (Aqua), Hydrofluorocarbon 152a, Isobutane, Emulsifying Wax NF, Cetyl Lactate, Steareth-2, Propane, Sodium Benzoate, Sodium Sesquicarbonate, Fragrance (Parfum)
  • INGREDIENTS AND APPEARANCE
    CARDINAL HEALTH SANITIZER 
    alcohol aerosol, foam
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63517-523
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.625 mg  in 1 mg
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    STEARETH-2 (UNII: V56DFE46J5)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63517-523-15 12 in 1 CASE
    1 425000 mg in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 02/24/2011
    Labeler - Cardinal Health (097537435)