HAND SANITIZER (ETHYL ALCOHOL) GEL [ULINE]

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HAND SANITIZER (ETHYL ALCOHOL) GEL [ULINE]
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NDC 69790-770-16
Set ID 3bc9cfa2-2b1f-4892-93ff-cffa9f587804
Category HUMAN OTC DRUG LABEL
Packager Uline
Generic Name
Product Class
Product Number
Application Number PART333A
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  • Active Ingredient

    Ethyl alcohol 70%

  • Purpose

    Antiseptic

  • Uses

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

    For external use only: hands

    Flammable.  Keep away from fire 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 or 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 thoroghly 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: ULINE
    12575 uline Drive, Pleasant Prairie, WI 53158
    1-800-295-5510 - uline.com

  • principal display panel

    ENRICHED WITH MOISTURIZERS

    ULINE

    Hand Sanitizer

    Kills more than 99.99% of germs*

    S-21262

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-770
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 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 COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69790-770-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/28/2016
    2NDC:69790-770-96221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/28/2016
    3NDC:69790-770-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/28/2016
    4NDC:69790-770-881999 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/28/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/28/2016
    Labeler - Uline (039612668)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(69790-770)
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