Label: SYMMETRY ANTIMICROBIAL FOAMING HAND WASH W/BENZALKONIUM CHLORIDE- benzalkonium chloride solution

  • NDC Code(s): 30805-017-02, 30805-017-07
  • Packager: Buckeye International, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2024

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

  • Active ingredient

    Benzalkonium Choride 0.13%

  • Purpose

    Antibacterial

  • Uses

    • Hand wash to help reduce bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only.

    When using this productdo not use in or near eyes.

    If in eyes, flush thoroughly with water.

    If irritation or rash appears and persists, stop use and see a physician.

    Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

  • Directions

    • Wet hands and wrists
    • Dispense an adequate amount of soap and vigorously wash hands
    • Rinse hands thoroughly
    • Dry hands completely
  • Inactive ingredients

    Water (Aqua), Cetrimonium Chloride, Tetrasodium EDTA, Phenoxyethanol, Citric Acid

  • Questions?

    Call: Buckeye International, Inc. 314-291-1900

    Monday through Friday 8:00 a.m. to 5:00 p.m. CST

  • PRINCIPAL DISPLAY PANEL

    Symmetry

    Antimicrobial

    Foaming

    Hand Wash

    w/ Benzakonium Chloride

    NSF

    Nonfood Compounds

    Program Listed (Category E2)

    Registration #XXXXXX

    Made in USA

    Product # XXXXXXXX

    Net Content 1250 ml (42.2 fl oz)

    container label

  • INGREDIENTS AND APPEARANCE
    SYMMETRY ANTIMICROBIAL FOAMING HAND WASH W/BENZALKONIUM CHLORIDE 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30805-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE SODIUM (UNII: MP1J8420LU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:30805-017-021250 mL in 1 BAG; Type 0: Not a Combination Product06/28/2022
    2NDC:30805-017-07550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/28/2022
    Labeler - Buckeye International, Inc. (077132280)
    Establishment
    NameAddressID/FEIBusiness Operations
    Buckeye International, Inc.077132280manufacture(30805-017)