Label: SAFEGUARD ANTIBACTERIAL FOAMING- benzalkonium chloride soap

  • NDC Code(s): 37000-601-40
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 1, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.12%

  • Purpose

    Antiseptic Hand Cleanser

  • Uses

    • For handwashing to decrease bacteria on the skin
    • Recommended for repeated use
  • Warnings

    • For external use only

    When using this product

    • Do not use in or near eyes

    • Discontinue use if irritation and redness develop

    Keep out of reach of children

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    • Wet hands and forearms
    • Apply enough product to adequately cover the entire surfaces of the hands and forearms
    • Scrub thoroughly for at least 30 seconds (include the fingernails and the cuticles)
    • Rinse
  • Other information

    • Store in a cool dry place below 104° F
  • Inactive ingredients

    Water, glycerine, cocoamidopropyl betaine, polyoxypropylene-polyoxyethylene block copolymer, benzyl alcohol, fragrance, phenoxyethanol, tetra sodium EDTA, dehydroacetic acid, FD&C Red #4, FD&C Yellow #5

  • Questions?

    Contact Procter & Gamble Professional® Mon-Fri 9am - 5pm EST at 1-800-332-7787

  • PRINCIPAL DISPLAY PANEL - 1.2 L Bag Label

    Procter & Gamble
    Professional ®

    Safeguard ®
    AntiBacterial

    Foaming Hand Soap
    Benzalkonium Chloride Foaming Antibacterial Hand Soap

    1.2L (1.26 QT) 40.5 FL OZ

    Principal Display Panel - 1.2 L Bag Label
  • INGREDIENTS AND APPEARANCE
    SAFEGUARD  ANTIBACTERIAL FOAMING
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-601
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.12 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Product Characteristics
    ColororangeScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-601-401200 mL in 1 BAG; Type 0: Not a Combination Product07/01/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/01/2010
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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