HAND SANITIZER HAND RX (ETHYL ALCOHOL) LIQUID [BLUE CROSS LABORATORIES, INC. ]

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  • HAND SANITIZER HAND RX (ETHYL ALCOHOL) LIQUID [BLUE CROSS LABORATORIES, INC. ]

HAND SANITIZER HAND RX (ETHYL ALCOHOL) LIQUID [BLUE CROSS LABORATORIES, INC. ]
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NDC 22431-581-01
Set ID 76d74b1b-ed40-4525-8556-b7a0485a75cb
Category HUMAN OTC DRUG LABEL
Packager Blue Cross Laboratories, Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
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  • ACTIVE INGREDIENT

    Active ingredients       purpose

    Ethyl Alcohol 62%       Antimicrobial        

    Kills over 99% of most common germs

    Keep out of reach of children

    Keep out of eyes.In case of eye contact immediately flush eyes with water then contact physician.

    Warning: flammable. Keep away from flame. If swallowed, contact physician. For external use only. Do not store above 110 degrees farenheit.

    directions:

    put a thumbnail size amount in your palm and rub your hands together briskly until dry

    Children under 6 years of age should be supervised when using Hand Rx.

    Inactive Ingredients: Water, Glycerin, Propylene Glycol, Carbomer

  • PRINCIPAL DISPLAY PANEL

    Hand Rx

    Hand Sanitizer

    Kills 99.99% of germs

    8 Fl Oz. (236 ml)

    back label

    front label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  HAND RX
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-581
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22431-581-01236 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
    2NDC:22431-581-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
    3NDC:22431-581-03118 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
    4NDC:22431-581-041180 mL in 1 BOTTLE; Type 0: Not a Combination Product10/12/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/12/2010
    Labeler - Blue Cross Laboratories, Inc. (008298879)
    Registrant - Blue Cross Laboratories, Inc. (008298879)
    Establishment
    NameAddressID/FEIBusiness Operations
    Blue Cross Laboratories, Inc.008298879manufacture(22431-581)
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