Label: AL-SHIELDS ANTIBACTERIAL HAND WIPES WITH FRESH ALOE SCENT- benzalkonium chloride cloth

  • NDC Code(s): 74934-037-01, 74934-037-02, 74934-037-03
  • Packager: Zhejiang iColor Biotech Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 23, 2024

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  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.1%

    Purpose

    Antibacterial 

  • Use

    Hand wipe to help reduce bacteria on the skin

  • Warning

    For external use only

    When using this product

    do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation or rash appears and lasts

    Keep out of reach of children.

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

  • Directions

    • Wet hands thoroughly with product and allow to dry
    • Discard wipes in trash receptacle after use. Do not flush
    • Children under 6 years of age should be supervised when using this product
  • Inactive Ingredients

    Ethylhexylglycerin, Glycerin, Phenoxyethanol, Polyaminopropyl biguanide, Propylene Glycol, Purified water, Fragrance

  • Questions or Comments?

    Call 1-855-929-3829 (M-F)

  • Package Labeling:10ct

    Label

  • Package Labeling:20ct

    Label2

  • Package Labeling:30ct

    Box

  • INGREDIENTS AND APPEARANCE
    AL-SHIELDS ANTIBACTERIAL HAND WIPES WITH FRESH ALOE SCENT 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74934-037
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74934-037-0110 in 1 BAG07/28/202001/31/2026
    14 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    2NDC:74934-037-0220 in 1 BAG07/28/202001/31/2026
    24 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    3NDC:74934-037-0330 in 1 BAG09/04/202001/31/2026
    34 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)07/28/202001/31/2026
    Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)
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