Label: BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING- ethyl alcohol spray

  • NDC Code(s): 53950-6010-1
  • Packager: Robanda International, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 8, 2023

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  • Active ingredient

    ETHANOL (Alcohol Denat.) 60.00%

  • Purpose

    Antimicrobial

  • uses

    Works instantly to effectively eliminate germs and bacteria from cosmetic products, tester displays, makeup kits, workstations or hands

  • Warnings

    Flammable. Keep away from fire or flame.
    Do not use in or near the eyes, in case of contact, rinse thoroughly with water.
    For external use only. Stop use and ask a doctor if irritation or rash appears and lasts. Avoid contact with broken skin.

    If swallowed, seek medical help immediately.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Directions

    • Hold spray 6” away from products, hands and surfaces, gently spray once or twice from one side to the other, in a swiping motion.
  • OTHER INFORMATION

    • Store between 15-30C (56-86F)
    • Avoid freezing and excessive heat about 40C (104F)
  • Inactive ingredients

    Water (aqua), Citrullus lanatus (Watermelon) Fruit Extract, Chenopodium quinoa Extract, Urea, Sucrose, Glycerin, Sodium Lactate, Sodium
    PCA, Phenoxyethanol, Ethylhexylglycerin, Caprylyl Glycol, Hexylene Glycol, Fragrance

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Bodyographypro_Antibacterial Cosmetic Sanitizer_4oz

  • INGREDIENTS AND APPEARANCE
    BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53950-6010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    WATER (UNII: 059QF0KO0R)  
    WATERMELON (UNII: 231473QB6R)  
    CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X)  
    UREA (UNII: 8W8T17847W)  
    SUCROSE (UNII: C151H8M554)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53950-6010-1118 mL in 1 BOTTLE; Type 0: Not a Combination Product08/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01408/15/2020
    Labeler - Robanda International, Inc. (048214287)
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