Label: 2XL MEGA ROLLS SANITIZING WIPES- benzalkonium chloride swab

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

Drug Label Information

Updated December 6, 2024

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  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

    • to sanitize hands without requiring water or a rinse
    • kills 99.9% of most common germs
  • Warnings

    For external use only

    When using this product

    • do not use in or near the eye
    • discontinue use if irritation and redness develop

    Keep out of reach of children

    In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.

  • Directions

    • wet hands thoroughly with wipe
    • allow to dry without rinsing
  • Other information

    Store at room temperature

  • Inactive ingredients

    Water, Phenoxyethanol, Decyl Glucoside, Potassium Sorbate, Sodium Benzoate, Disodium EDTA,  Citric Acid, Aloe Barbadensis  (Aloe)  Leaf Extract, Fragrance

  • Questions? Comments?

    Call (888)977-3726

  • Principal Display Panel

    NDC 71995-020-01

    Kills 99.9% of most common germs that may cause illness

    2XL Mega ROLL

    2.3K

    SANITIZING WIPES

    2300 count megaroll

    • Quickly removes soil and kills most common germs that may cause illness
    • Textured for superior cleaning
    • Sanitizes hand while cleaning effectively
    • Convenient, easy to use and ideal for placement in offices, restaurants, health clubs, or anywhere else germs may be

    NET CONTENTS 2300 Wipes per Roll (8'' X 5'')

    Net Weight: 5460g/roll

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  • INGREDIENTS AND APPEARANCE
    2XL MEGA ROLLS SANITIZING WIPES 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71995-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71995-020-012300 in 1 BAG01/02/2018
    11 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/16/2017
    Labeler - 2xl Corporation (148004059)
    Registrant - 2xl Corporation (148004059)
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