Label: BIG WIPES MULTI-PURPOSE- benzalkonium chloride cloth

  • NDC Code(s): 79705-002-01, 79705-002-03, 79705-002-04, 79705-002-06
  • Packager: Sycamore USA Inc.
  • Category: HUMAN OTC DRUG LABEL

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 November 23, 2022

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    Ceans hands and reduces bacteria on the skin

  • Warnings

    For external use only

    When using this product do not use in or around eyes. May irritate eyes.

    If IN EYES rinse well for 15 minutes

    KEEP OUT OF REACH OF CHILDREN

  • Directions

    Open foil seal and pull the center wipe through the lid

    • Wipe hands
    • For best results, clean spills immediately
    • Always shut the lid after use and store at room temperature.
  • Inactive ingredients

    WATER (AQUA), DIMETHYL SUCCINATE, DIMETHYL GUTARATE, DIMETHYL ADIPATE, DIMETHYL METHYLGLUTARATE. POLYSORBATE-80, POLYSORBATE-20, DIDECYLDIMONIUM CHLORIDE, GLYCERIN, METHYL SOYATE, PEG-75 LANOLIN, ALCOHOL, CITRIC ACID, SODIUM CITRATE, ALOE BARBADENSIS LEAF JUICE, TOCOPHERYL ACETATE (VITAMIN E), PROPANEDIOL, PARFUM.

  • Questions?

    Call (770) 628-0286 or visit www.bigwipesusa.com

  • PRINCIPAL DISPLAY PANEL

    BIG WIPES

    MULTI-PURPOSE

    ANTIBACTERIAL HAND WIPES

    PRO+

    CLEANS

    PAINT

    ADHESIVE

    SILICONE

    POLY FOAM

    GAP FILL

    OIL

    GRIME

    and MORE FROM

    YOUR HANDS

    4x4 FORMULA

    TOUGH ON

    GRIME

    KIND TO YOUR HANDS

    NDC # 79705-002-04

    ANTIBACTERIAL

    check mark

    Hand Wipes

    NSF

    Nonfood Compound

    E4

    DERMATOLOGICALLY TESTED

    80

    WIPES (8" x 12")

    HAND SANITIZER WIPES

    container label

  • INGREDIENTS AND APPEARANCE
    BIG WIPES MULTI-PURPOSE 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79705-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    METHYL SOYATE (UNII: 808DL597QP)  
    DIMETHYL GLUTARATE (UNII: 1I9VFA346P)  
    DIMETHYL METHYLGLUTARATE (UNII: 728OFW5M9G)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHYL SUCCINATE (UNII: 914I2127JR)  
    DIMETHYL ADIPATE (UNII: BY71RX0R62)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79705-002-014 mL in 1 POUCH; Type 0: Not a Combination Product08/31/2020
    2NDC:79705-002-03110 mL in 1 CANISTER; Type 0: Not a Combination Product08/31/2020
    3NDC:79705-002-04310 mL in 1 CANISTER; Type 0: Not a Combination Product08/31/2020
    4NDC:79705-002-061161 mL in 1 CANISTER; Type 0: Not a Combination Product08/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/31/202010/31/2025
    Labeler - Sycamore USA Inc. (078589316)
    Establishment
    NameAddressID/FEIBusiness Operations
    WET NAPS LTD.514650902manufacture(79705-002)
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