Label: CARDINAL HEALTH SANITIZER- alcohol aerosol, foam

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 24, 2011

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  • 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 Flammable.
    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)
  • PRINCIPAL DISPLAY PANEL

    image
  • INGREDIENTS AND APPEARANCE
    CARDINAL HEALTH SANITIZER 
    alcohol aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63517-523
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.625 mg  in 1 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    STEARETH-2 (UNII: V56DFE46J5)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63517-523-1512 in 1 CASE
    1425000 mg in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/24/2011
    Labeler - Cardinal Health (097537435)
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