Label: ANTIMICROBIAL HAND WIPES cloth

  • 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 22, 2022

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  • Active Ingredient

    Active Ingredient

    Benzalkonium Chloride 0.125%

  • Purpose

    Pupose

    Antimicrobial

  • Uses

    Uses

    * For hand washing to decrease bacteria on skin without requiring water or rinsing

    * Recommended for repeated use

  • Warnings

    Warnings

    For external use only

  • When using this product

    When using this product

    * Do not use in or near eyes

    If contact occurs, rinse eyes thoroughly with water

  • Stop use and ask a doctor

    Stop use and ask a doctor

    *If irritation and redness persist for more than 72 hours

  • Keep Out of reach of children

    Keep out of reach of children

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    Directions

    * Wet thoroughly hands with wipe and allow to dry without wiping.

    * Children under six years of age should be supervised when using this product

  • Inactive Ingredients

    Inactive Ingredients

    Aloe Barbadensis Leaf Juice, Citric Acid, Decyl Glucoside, Fragrance, Phenoxyethanol, Potassium Sorbate, Tetrasodium EDTA, Water.

  • Principal Display Panel

    LabelKILLS 99.9% OF GERMS

    all clear

    Antibacterial Hand Wipes

    Helps keep hands clean while on-the-go

    7 x 5.1in (18 x 13cm)

    20ct

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL HAND WIPES 
    antimicrobial hand wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77070-701
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.125 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77070-701-201 g in 1 POUCH; Type 0: Not a Combination Product07/11/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/11/2020
    Labeler - Goodfibers (105870470)
    Registrant - Goodfibers (105870470)
    Establishment
    NameAddressID/FEIBusiness Operations
    Goodfibers105870470manufacture(77070-701)
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