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 30142-596-16, 30142-596-34, 30142-596-45
Set ID 9f95d956-25db-4ffa-86cc-a160677124b8
Category HUMAN OTC DRUG LABEL
Packager The Kroger Co
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active ingredients

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

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

    For external use only: hands

  • Flammable

    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

    • irritation and redness develop
    • 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 105⁰ F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

  • SPL UNCLASSIFIED SECTION

    Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.*

    DISTRIBUTED BY: KROGER CO

    CINCINNATI, OHIO 45202

    QUALITY GUARANTEE

    800-632-6900 www.kroger.com

  • principal display panel

    Kroger

    ORIGINAL SCENT

    HAND SANITIZER

    KILLS 99.99% OF GERMS

    32 FL OZ (946 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-596
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30142-596-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2012
    2NDC:30142-596-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2012
    3NDC:30142-596-45945 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/17/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/17/2012
    Labeler - The Kroger Co (006999528)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(30142-596)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(30142-596)
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