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

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 31, 2019

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

  • Active ingredient

    Benzalkonium chloride 0.13%

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  • Purpose

    Antimicrobial

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  • Uses

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

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  • Directions

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

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  • Other information

    Store at room temperature

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  • Inactive ingredients

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

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  • Questions? Comments?

    Call (888)977-3726

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  • 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

    Label

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  • INGREDIENTS AND APPEARANCE
    2XL MEGA ROLLS SANITIZING WIPES 
    benzalkonium chloride swab
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:71995-020
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:71995-020-01 2300 in 1 BAG 01/02/2018
    1 1 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 03/16/2017
    Labeler - 2xl Corporation (148004059)
    Registrant - 2xl Corporation (148004059)
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