WATERLESS HAND SANITIZER (ALCOHOL) GEL [ONPOINR, INC]

WATERLESS HAND SANITIZER (ALCOHOL) GEL [ONPOINR, INC]
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NDC 51143-203-34
Set ID 2b764da7-370c-4eab-9214-c8c260583419
Category HUMAN OTC DRUG LABEL
Packager Onpoinr, Inc
Generic Name
Product Class
Product Number
Application Number PART333A
  • Active Ingredient

    Ethyl Alcohol 65%

    Purpose

    Antiseptic

  • Use

    •to decrease bacteria on the skin that could cause disease
    •recommended for reported 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.
    •do not inhale or ingest
    •avoid contact with broken skin

    Stop use and ask a doctor if

    skin irritation develops

    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  •may discolor some fabrics
    •harmful to wood finishes and plastics

  • Inactive ingredients

    aloe barbadensis leaf juice, benzophenone-4, blue 1, carbomer, fragrance, glycerin,
    isopropyl myristate, propylene glycol, tocopheryl acetate, water, yellow 5

  • SPL UNCLASSIFIED SECTION

    Not manufactured or distributed by GOJO Industries, owner of the registered trademark Purell

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

    Distributed by: Onpoint, Inc
    2 Paragon Drive,
    Montvale, NJ 07645

  • PRINCIPAL DISPLAY PANEL

    Live Better
    Waterless Hand Sanitizer With Aloe
    •Kills 99.99% of Germs
    8 FL OZ (236 mL)

    image of principal display panel

    203.000/203AB

  • INGREDIENTS AND APPEARANCE
    WATERLESS HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51143-203
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL.65 mL  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51143-203-34.236 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/01/2011
    Labeler - Onpoinr, Inc (001367366)
    Registrant - Vi-Jon (088520668)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon088520668manufacture(51143-203)

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