Label: T3 WOUND WASH- benzalkonium chloride solution

  • NDC Code(s): 72053-004-04
  • Packager: Patient Focused Telehealth
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 13, 2024

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  • Active Ingredient

    Benzalkonium Chloride (0.1% by volume)

  • purpose

    Antiseptic

  • Use

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

  • Warnings

    For external use only

  • When using this product

    Avoid contact with eyes

  • stop use and ask a doctor if

    the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a poison control center right away.

  • Directions

    • Clean the affected area
    • Apply a small amount of this product on the area 1 to 3 times daily
    • Allow to dry
    • Cover the affected area with sterile bandage if needed
    • When bandaged, let dry first
  • Other Information

    Store at 40 to 120 F

  • Inactive Ingredients

    ascorbic acid, aloe barbadensis leaf juice, carbomer, cholecalciferol, citric acid, dimethyl sulfoxide, diazolidinyl urea, dipropylene glycol, dmdm hydantoin, glycerin, polysorbate 20, sodium dodecylbenzene sulfonate, tetrasodium EDTA, triethanolamine, tocopheryl acetate (vitamin E acetate), water

  • Questions

    Tel. 800-918-7534 Email Address: info@patientfocusedtelehealth.com Manufactured by: TG Labs, LLC 7318 S Revere Pkwy, Centennial CO 80112 For: Patient focused tele-health LLC, 400 Country Ridge, Rockwall, TX USA 75087

  • Principal Display Panel

    Front PanelT3 Wound Wash

    Benzalkonium Chloride 0.1%

    First Aid Antiseptic Solution

    1 FL OZ 30 mL

  • INGREDIENTS AND APPEARANCE
    T3 WOUND WASH 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72053-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.03 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72053-004-0430 mL in 1 BOTTLE; Type 0: Not a Combination Product07/25/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/25/2022
    Labeler - Patient Focused Telehealth (081008911)
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