Label: BEST ACCESSORY GROUP COTTON CANDY SCENTED HAND SANITIZER- alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 22, 2019

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  • Drug Facts

  • Active ingredient

    Alcohol 62%

  • Purpose

     Antiseptic

  • Use

    Decreases bacteria on hands.

  • Warnings

    For external use only.

    Flammable.Keep product away from fire or flame.

    When using this product

    avoid contact with eyes; in case of contact, flush eyes with water.

    Stop use and ask a doctor if

    irritation or redness develops and persists.

    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.

  • Inactive ingredients

    Water (Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum). May Contain: D&C Red No.33 (CI 17200), FD&C Red No.4 (CI 14700), FD&C Yellow No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

  • SPL UNCLASSIFIED SECTION

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

    Distributed by 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#: FB9400AW

    WARNING - CHOKING HAZARD

    Small Parts. Not for children under 3 years.

    NO ANIMAL TESTING.

    NEW!

    2 in 1

    Anti - Bacterial Sanitizer with Holder

    www.mybeautyspot.com

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    BEST ACCESSORY GROUP COTTON CANDY SCENTED HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60533-014
    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 INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Other Ingredients
    Ingredient KindIngredient NameQuantity
    May containD&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    May containFD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    May containFD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    May containFD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60533-014-2929 mL in 1 BOTTLE; Type 0: Not a Combination Product07/22/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/22/2019
    Labeler - Best Accessory Group (078712219)
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