Label: SAFEGUARD ANTIBACTERIAL FOAMING- benzalkonium chloride soap

  • NDC Code(s): 37000-601-40
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL

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 January 31, 2023

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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 finalM00507/01/2010
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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