VANILLA CUPCAKE ANTI-BACTERIAL SCENTED HAND SANITIZER (ALCOHOL) SOLUTION [BEST ACCESSORY GROUP]

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VANILLA CUPCAKE ANTI-BACTERIAL SCENTED HAND SANITIZER (ALCOHOL) SOLUTION [BEST ACCESSORY GROUP]
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NDC 60533-011-29
Set ID 277f8648-d828-40db-9bcd-f141251110d3
Category HUMAN OTC DRUG LABEL
Packager Best Accessory Group
Generic Name
Product Class
Product Number
Application Number PART333E
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  • SPL UNCLASSIFIED SECTION

    OUR POWERFUL GERM-KILLING FORMULA LEAVES HANDS FEELING FRESH AND CLEAN !

    Drug Facts

  • Active Ingredient:

    Alcohol 62%

  • PURPOSE

    Purpose:Antiseptic

  • INDICATIONS & USAGE

    Use: Decreases bacteria on hands.

  • Warnings:

    For External Use Only.

  • WHEN USING

    Flammable -Keep product away from fire or flame.

  • WHEN USING

    When using this product avoid contact with eyes; in case of contact, flush eyes with water.

  • STOP USE

    Stop use & ask a doctor if irritation or redness develops and persists.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions: Wet hands thoroughly with product and allow to dry.

  • Inactive Ingredients:

    Water(Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Triethanolamine, PEG-40 Hydrogenated Castor Oil, Fragrance (Parfum), Jojoba Esters. May Contain: D&C RED No.33 (CI 17200), FD&C BLUE No. 1 (CI 42090)

    NO ANIMAL TESTING

  • SPL UNCLASSIFIED SECTION

    B•A•G

    BEST ACCESSORY GROUP

    10 West 37th st. Suite 4E New York NY, 10018
    Rue de la Victoire 26 Suite: 132494, 1060
    Brussels, Belgium
    Designed in USA. Made in China
    Item#: VC3178

  • PRINCIPAL DISPLAY PANEL - 29 mL Bottle Label

    Vanilla
    cupcake

    antibacterial

    SCENTED
    HAND SANITIZER

    1 fl.oz - 29 mL

    PRINCIPAL DISPLAY PANEL - 29 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    VANILLA CUPCAKE ANTI-BACTERIAL SCENTED HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60533-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    ETHYL JOJOBATE (UNII: 2351QH8W1N)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60533-011-2929 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/13/2013
    Labeler - Best Accessory Group (078712219)
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