Label: WET WIPES ANTIBACTERIAL HAND WIPES, TRAVEL PACK- benzethonium chloride cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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

  • Drug Facts

  • Active Ingrdient

    Benzethonium Chloride 0.13%

    Purpose

    Antimicrobial

  • Uses

    • for hand sanitizing to decrease bacterial on skin
    • recommended for repeated use
  • WARNINGS

    For external use only

    When using this product

    avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation or redness develop

    Keep out of reach of children.

    if swallowed, get medical help or contact a Poisin Control Center right away.

  • Directions

    • take wipe and rub thoroughly over all surfaces of both hands
    • rub hands together briskly to dry
    • dispose of wipe
  • Inactive Ingredients:

    Purified Water, Glycerin, Phenoxyethanol, Polysorbate 20, Tocopheryl Acetate, Polyhexamethylene Biguanide, Citric Acid, Aloe Barbadesis Leaf Juice (Aloe Vera).

  • Package labeling:

    LabelLabel 02

  • INGREDIENTS AND APPEARANCE
    WET WIPES ANTIBACTERIAL HAND WIPES, TRAVEL PACK 
    benzethonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72146-037
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POLIHEXANIDE (UNII: 322U039GMF)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72146-037-011 in 1 PACKAGE12/01/2024
    130 in 1 POUCH
    1114.9 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/01/2024
    Labeler - TARGET PRICE INC (081086884)