Label: DIAL PROFESSIONAL ANTIBACTERIAL HAND SANITIZER- ethyl alcohol liquid

  • 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 March 16, 2011

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  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl Alcohol 72%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses

    hand sanitizer to help reduce bacteria that potentially may cause disease

  • WARNINGS

    Warnings

    For external use only

    Flammable.  Keep away from fire or flame.

    When using this product

    avoid contact with face, eyes, and broken skin.  If eye contact occurs, flush thoroughly with water and seek medical advice.

    Stop use and ask a doctor if

    irritation and redness develops

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

  • DOSAGE & ADMINISTRATION

    Directions

    pump foam into dry hands, wet thoroughly and rub into skin until dry

    Children under 6 years of age should be supervised by an adult when using this product.

  • INACTIVE INGREDIENT

    Inactive ingredients

    water, n-propanol, bis-PEG-12 dimethicone, behentrimonium chloride, PEG-200 hydrogenated glyceryl palmate, PEG-7 glyceryl cocoate, coco-glucoside, glyceryl linoleammonium chloride

  • QUESTIONS

    Questions?

    1-877-777-3277

  • PRINCIPAL DISPLAY PANEL

    Dial Professional

    Antibacterial Hand Sanitizer Fragrance Free Foam

    Kills 99.99% of germs instantly

    Made in Canada

    2010 Distributed by The Dial Corporation/A Henkel Company

    Scottsdale, AZ 85255

    www.dialprofessional.com

    Install with label toward wall

    Instalar con etiqueta hacia la pared

    US Patent Numbers

    5445288, 6082586, patent pending

    1 Liter (33.8 Fl Oz)

    1 QT 1.8 Fl Oz

    Latex and Non-latex compatible

    Tested on latex and nitrile gloves.

    container label

  • INGREDIENTS AND APPEARANCE
    DIAL PROFESSIONAL ANTIBACTERIAL HAND SANITIZER  
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-107
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol72 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
    PROPYL ALCOHOL (UNII: 96F264O9SV)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-107-271000 mL in 1 BOTTLE, PLASTIC
    2NDC:54340-107-121000 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/01/2010
    Labeler - The Dial Corporation (070252531)
    Establishment
    NameAddressID/FEIBusiness Operations
    Deb Worldwide Healthcare Inc.205662831manufacture
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