Label: ACTIVE GUARD- benzalkonium chloride liquid

  • NDC Code(s): 73746-037-01, 73746-037-02, 73746-037-03
  • Packager: HOME & BODY COMPANY
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 13, 2022

If you are a consumer or patient please visit this version.

  • Active ingredient

    0.13% Benzalkonium Chloride

  • Purpose

    Antibacterial

  • Use

    Helps reduce bacterial on hands

  • Warning

    For external use only.
    When using this product do not use in or near the eyes.
    In case of contact, rinse eyes throughly with water.

  • Keep out of reach of children

    Keep out of reach of children, except under adult supervision. If swallowed, get medical help or
    contact a Poison Control Center right away.

  • Directions

    Dispense soap into dry hands, work into lather and scrub for at least 35 seconds. Then rinse off with water.

  • Inactive Ingredients

    Water (Aqua), Lauramine Oxide, Cellulose Gum, Tetrasodium EDTA, Polysorbate 20, Fragrance, Glycerin, Cocamidopropyl Betaine

  • DOSAGE & ADMINISTRATION

  • Product Label

    24 front24 back32 front32 back16

  • INGREDIENTS AND APPEARANCE
    ACTIVE GUARD 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73746-037
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE SODIUM (UNII: MP1J8420LU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73746-037-01946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2020
    2NDC:73746-037-02724 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2020
    3NDC:73746-037-03473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/29/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/29/2020
    Labeler - HOME & BODY COMPANY (081290720)
    Registrant - HOME & BODY COMPANY (081290720)
    Establishment
    NameAddressID/FEIBusiness Operations
    HOME & BODY COMPANY081290720manufacture(73746-037)