Label: GERMISEPT ANTIBACTERIAL HAND SANITIZING WIPES- benzalkonium chloride cloth

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

Drug Label Information

Updated December 21, 2023

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.1%

    Purpose

    Antibacterial

  • Uses:

    Decrease bacteria on the skin.

  • Warnings

    • For external use only.

    When using this product

    • avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Do not use

    if irritation and redness develop.

    Stop use and ask a doctor 

    if condition persists for more than 72 hours.

    Keep out of reach of children.

    If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    • Open the flip top lid, remove one wipe to use.
    • Wipe hands thoroughly the product and allow to dry without wiping.
    • Close flip top lid after use to retain moisture.
  • Other information

    • Dispose of wipe in the proper container.
    • Do not flush down the toilet.

    *Kill Claims Against: E.Coli & Staphylococcus.

  • Inactive ingredients

    2-Bromo-2-Nitropropane-1,3-Diol, Alcohol, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Fragrance, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Water.

  • Package Labeling:

    Bag3

  • INGREDIENTS AND APPEARANCE
    GERMISEPT ANTIBACTERIAL HAND SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70335-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BRONOPOL (UNII: 6PU1E16C9W)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70335-012-014 in 1 BAG02/10/2021
    150 in 1 PACKAGE
    14.3 mL in 1 PATCH; 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)02/10/2021
    Labeler - Innovent Inc (079973489)
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