Label: ANTIBACTERIAL SKIN- benzalkonium chloride lotion

  • NDC Code(s): 76176-207-01
  • Packager: NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 25, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated 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.
    • avoid contact with broken skin
    • do not inhale or ingest
  • 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 105℉
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    Water(Aqua), Mineral Oil, Cetearyl Alcohol, Petrolatum, Glyceryl Stearate, Ceteareth-25, Ammonium Polyacrylate, C13-16 Isoparaffin, Laureth-30, Fragrance, Glycerin, Carbomer, Propylene Glycol, Dimethicone, Methylisothiazolinone, Iodopropynyl Butylcarbamate

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL SKIN 
    benzalkonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-207
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    C13-16 ISOPARAFFIN (UNII: LED42LZG6O)  
    LAURETH-30 (UNII: W9D845551A)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CETEARETH-25 (UNII: 8FA93U5T67)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-207-01118 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/20/2024
    Labeler - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098)
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