Label: ANTISEPTIC WASH- 0.130% benzalkonium antiseptic wash liquid

  • NDC Code(s): 60232-0022-8
  • Packager: Swiss-American CDMO, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 7, 2023

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  • Warnings

    For external use only. Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center right away. Do not use on deep or puncture wounds, animal bites or serious burns

  • Use and Directions

    First aid to help prevent infection in minor cuts, scrapes and burns.

    Use on adults and children 2 years and older. Use to clean minor cuts, scrapes and burns by thoroughly flushing the affected area. Let air dry. Cover with an adhesive bandage or sterile gauze. Use no more than 2 times daily. Children under 2 years of age: ask a doctor.

  • Keep out of reach of children

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

  • Active Ingredient

    Benzalkonium Chloride 0.130%

  • PURPOSE

  • Inactive Ingredient

    Aloe Barbadensis Leaf Juice, Disodium EDTA, Poloxamer 188, Purified Water, Sodium Chloride, Sodium Citrate

  • Labeling

    PL022 Artwork

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC WASH 
    0.130% benzalkonium antiseptic wash liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60232-0022
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1000 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POLOXAMER 188 (UNII: LQA7B6G8JG)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60232-0022-8240 g in 1 BOTTLE; Type 0: Not a Combination Product09/05/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/05/2013
    Labeler - Swiss-American CDMO, LLC (080170933)
    Registrant - Swiss-American CDMO, LLC (080170933)
    Establishment
    NameAddressID/FEIBusiness Operations
    Swiss-American CDMO, LLC080170933manufacture(60232-0022)
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