Label: JUSTICE DIAMOND VANILLA SCENTED ANTIBACTERIAL HAND SANITIZER- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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  • Drug Facts

  • Active ingredient

    Alcohol 62%

    Purpose

    Antiseptic

  • Use

    • for hand-washing to decrease bacteria on the skin, 
    • Recommended for repeated area
  • Warnings

    Flammable, keep away from fire or flames

    For external use only

    Do not use

    in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animals bites, or serious burns, consult a doctor. Use only as directed.  Do not drink. If taken internally, it will produce serious gastric disturbances.


    Stop use and ask a doctor if

    • Irritation 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 thoroughly with product and allow to dry without wiping
    • Supervise children in the use of this product.
  • Inactive ingredients

    Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl Propanol, Mica, Red 40.

  • Other information

    • Store below 105°F (40.5°C).
    • May discolor some fabrics: Expiry Date 10/2022
  • Package Labeling:

    Label5

  • INGREDIENTS AND APPEARANCE
    JUSTICE DIAMOND VANILLA SCENTED ANTIBACTERIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60637-194
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    MICA (UNII: V8A1AW0880)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60637-194-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product10/08/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/08/2019
    Labeler - Tween Brands,Inc. (965758188)
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