Label: ANTIBACTERIAL LAVENDER SCENT- benzalkonium chloride liquid
ANTIBACTERIAL LEMON SCENT- benzalkonium chloride liquid
ANTIBACTERIAL WATERMELON SCENT- benzalkonium chloride liquid
ANTIBACTERIAL- benzalkonium chloride liquid
ANTIBACTERIAL COTTON SCENT- benzalkonium chloride liquid

  • NDC Code(s): 71788-017-10, 71788-017-20, 71788-017-50, 71788-017-60, view more
    71788-017-70, 71788-017-80, 71788-018-10, 71788-018-20, 71788-018-50, 71788-018-60, 71788-018-70, 71788-018-80, 71788-019-10, 71788-019-20, 71788-019-50, 71788-019-60, 71788-019-70, 71788-019-80, 71788-020-10, 71788-020-20, 71788-020-50, 71788-020-60, 71788-020-70, 71788-020-80, 71788-021-10, 71788-021-20, 71788-021-50, 71788-021-60, 71788-021-70, 71788-021-80
  • Packager: Protect U Guard LLC
  • 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 July 31, 2023

If you are a consumer or patient please visit this version.

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Skin Antimicrobial

  • Uses

    reduces amount of bacteria on hands

  • Warnings

    For external use only: hands.

  • When using this product

    do not use in or near eyes. In case of eye contact, flush thoroughly with water. Do not inhale or ingest.

  • Stop use and ask doctor if

    irritation or redness develops. condition persists for more than 72 hours

  • Keep out of reach of children.

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

  • Directions

    Dispense an adequate amount in your palm to cover all surfaces of both hands completely. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry

  • Inactive ingredients

    Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Parfum.

  • Questions or comments?

    813-815-0530 or www.protectuguard.com

  • PRINCIPAL DISPLAY PANEL

    Antibacterial Soap 71788_017Lemon Soap 71788_018Lavender Soap 71788_019Watermelon Soap 71788_020Cotton Soap 71788_021

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL LAVENDER SCENT 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71788-019
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    WATER (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71788-019-7024 in 1 CARTON12/02/2021
    1NDC:71788-019-80100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:71788-019-5012 in 1 CARTON12/02/2021
    2NDC:71788-019-60530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:71788-019-104 in 1 CARTON12/02/2021
    3NDC:71788-019-201000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/02/2021
    ANTIBACTERIAL LEMON SCENT 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71788-018
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    WATER (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71788-018-7024 in 1 CARTON12/02/2021
    1NDC:71788-018-80100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:71788-018-5012 in 1 CARTON12/02/2021
    2NDC:71788-018-60530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:71788-018-104 in 1 CARTON12/02/2021
    3NDC:71788-018-201000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/02/2021
    ANTIBACTERIAL WATERMELON SCENT 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71788-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    WATER (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71788-020-7024 in 1 CARTON12/02/2021
    1NDC:71788-020-80100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:71788-020-5012 in 1 CARTON12/02/2021
    2NDC:71788-020-60530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:71788-020-104 in 1 CARTON12/02/2021
    3NDC:71788-020-201000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/02/2021
    ANTIBACTERIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71788-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    WATER (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71788-017-7024 in 1 CARTON12/02/2021
    1NDC:71788-017-80100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:71788-017-5012 in 1 CARTON12/02/2021
    2NDC:71788-017-60530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:71788-017-104 in 1 CARTON12/02/2021
    3NDC:71788-017-201000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/02/2021
    ANTIBACTERIAL COTTON SCENT 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71788-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    WATER (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71788-021-7024 in 1 CARTON12/02/2021
    1NDC:71788-021-80100 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:71788-021-5012 in 1 CARTON12/02/2021
    2NDC:71788-021-60530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    3NDC:71788-021-104 in 1 CARTON12/02/2021
    3NDC:71788-021-201000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/02/2021
    Labeler - Protect U Guard LLC (080070945)
    Establishment
    NameAddressID/FEIBusiness Operations
    Protect U Guard LLC080070945manufacture(71788-017, 71788-018, 71788-019, 71788-020, 71788-021)
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