Label: ANTIBACTERIAL HAND WIPES WITH ALOE- benzalkonium chloride cloth

  • NDC Code(s): 69446-210-30
  • Packager: Ez Products Of South Florida, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 23, 2023

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.11%

    Purpose

    Antiseptic

  • Uses

    • For handwashing to decrease bacteria on the skin
  • Warnings:

    For external use only.

    Do not use

    • in the eyes
    • Do not flush 
    • Discontinue use if irritation and redness develops. If eye contact occurs, rinse eyes thoroughly with water. If condition persists for more than 72 hours, consult a doctor.

    Keep out of reach of children.

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

  • Directions

    • Open resealable label, remove one wipe to use.
    • Wipe hands thoroughly with product and allow to dry without wiping.
    • Close resealable label after use to retain moisture.
  • Other information

    • Dispose of wipe in trash receptacle.
    • Do not flush down toilet.
  • Inactive Ingredients

    2-Bromo-2-Nitropropane-1,3-Diol, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Sodium Citrate, Tetrasodium EDTA, Water

  • Package Labeling:

    LabelBox

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND WIPES WITH ALOE 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69446-210
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BRONOPOL (UNII: 6PU1E16C9W)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69446-210-3030 in 1 POUCH09/01/2020
    12.94 g 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)09/01/2020
    Labeler - Ez Products Of South Florida, LLC (113456060)
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