Label: INSTANT HAND SANITIZER ORIGINAL- 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 30, 2011

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Ethyl Alcohol 62.0%

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    USE: hand sanitizer to help reduce bacteria on the skin that may cause disease.

  • WARNINGS

    Warnings: for external use only.

    Flammable. Keep away from heat and flame.

    When using this product

    • avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

    Stop use and ask a doctor if irritation or redness develops.

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

  • DOSAGE & ADMINISTRATION

    Directions

    • wet hands thoroughly with product and rub into skin until dry.
    • children under 6 years of age should be supervised by an adult when using.
  • INACTIVE INGREDIENT

    Inactive Ingredients:Water (Aqua), Triethanolamine, Carbomer, Aloe Vera Leaf Juice, Fragrance, Tocopheryl Acetate.

  • PRINCIPAL DISPLAY PANEL

    Kills 99.9% Germs without water or towels.


    Instant Hand Sanitizer

    Original

    Day2Day


    12 FL OZ (354ml)

    Instant Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER ORIGINAL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76088-300
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76088-300-12354 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/02/2011
    Labeler - King Import Warehouse (805424678)
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