HAND SANITIZER (ETHYL ALCOHOL) GEL [THE KROGER CO]

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HAND SANITIZER (ETHYL ALCOHOL) GEL [THE KROGER CO]
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NDC 30142-976-16
Set ID fcce5f61-a259-4afa-ac5d-ced8d2281c80
Category HUMAN OTC DRUG LABEL
Packager The Kroger Co
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active ingredient

    Ethyl alcohol 63%

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    For external use only: hands

  • Flammable

    Keep away from heat and flame

  • when using this product

    • keep out of eyes.  In case of contact with eyes, flush thoroughly with water
    • avoid contact with broken skin
    • do not inhale or ingest
  • Stop use and ask a doctor

    • if irritation and redness develops
    • condition persists for more than 72 hours
  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    • wet hands thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants
  • Other information

    • do not store above 105⁰F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, glycerin, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, benzophenone-4, fragrance, yellow 5, blue 1, red 4

  • adverse reactions section

    DISTRIBUTED BY THE KROGER CO.,

    CINCINNTI, OHIO 45202

    QUALITY GUARANTEE

    800-632-6900 -  www.kroger.com

    976.000/976AA

  • disclaimer

    EFFECTIVE AT ELIMINATING 99.99% OF MANY COMMON HARMFUL GERMS AND BACTERA IN AS LITTLE AS 15 SECONDS.

  • principal display panel

    KIWI PUNCH

    Kroger

    HAND SANITIZER

    KILLS 99.99% OF GERMS

    2 FL OZ (59mL)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-976
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL567 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-976-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/08/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/08/2016
    Labeler - The Kroger Co (006999528)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(30142-976)
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