Label: ATERRA7 ANTIBACTERIAL FOAMING HAND- benzalkonium chloride soap

  • NDC Code(s): 68306-115-01, 68306-115-02, 68306-115-03
  • Packager: B4 Ventures LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 27, 2023

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

  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Skin Antimicrobial

  • Use

    reduces amount of bacteria on hands

  • Warnings

    For external use only.

    When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

    Stop use and ask a doctorif irritation or redness develops, or if 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

    • Apply a palmful to hands and forearms.
    • Scrub thoroughly for at least 15 seconds.
    • Rinse completely and dry.
  • Inactive Ingredients

    Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance

  • PRINCIPAL DISPLAY PANEL

    Product Label - 1000 mL Cartridge - FrontProduct Label - 1000 mL Cartridge - Back

  • INGREDIENTS AND APPEARANCE
    ATERRA7 ANTIBACTERIAL FOAMING HAND 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-115
    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
    WATER (UNII: 059QF0KO0R)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    Product Characteristics
    Colorwhite (water white, colorless - dispensed as white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68306-115-01530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/26/2018
    2NDC:68306-115-024 in 1 BOX09/26/2018
    21000 mL in 1 BAG; Type 0: Not a Combination Product
    3NDC:68306-115-034 in 1 BOX09/20/2019
    31000 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 Drug505G(a)(3)09/26/2018
    Labeler - B4 Ventures LLC (133582853)