HAND SANITIZER (ETHYL ALCOHOL) SPRAY [VI- JON, INC]

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  • HAND SANITIZER (ETHYL ALCOHOL) SPRAY [VI- JON, INC]

HAND SANITIZER (ETHYL ALCOHOL) SPRAY [VI- JON, INC]
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NDC 11344-717-20
Set ID d20e2a54-26ba-438b-84c8-3a24b4bd3b5f
Category HUMAN OTC DRUG LABEL
Packager Vi- Jon, LLC
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active ingredient

    Ethyl alcohol 63%

  • purpose

    Antiseptic

  • Use

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

    For external use only

    Flammable.  Keep away from fire or 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 or 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

    • spray 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 105°F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, glycerin, tocopheryl acetate, Aloe barbadensis leaf juice, fragrance

  • Questions

    1-866-MYGERMX

    1-866-694-3769

  • claims

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

  • Adverse reaction

    Distributed By: Vi-Jon, LLC

    8515 Page AVe., St. Louis, MO 63114

    www.germx.com

  • principal display panel

    germ-X

    NATURAL

    Hand

    Sanitizer

    Spray

    Dye Free

    with Aloe

    Kills 99.99% Of Germs

    Vanilla Citrus

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-717
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol.63 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11344-717-2059 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/06/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/06/2016
    Labeler - Vi- Jon, LLC (150931459)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC150931459manufacture(11344-717)
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