Label: ATERRA7 ANTIBACTERIAL FOAMING HAND FRAGRANCE FREE- benzalkonium chloride solution

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

Drug Label Information

Updated October 23, 2024

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 doctor if 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

  • Questions or Comments?

    1-888-667-6066 or www.b4brands.com

  • PRINCIPAL DISPLAY PANEL

    Product Label - 1 Gallon Short Neck Bottle

  • INGREDIENTS AND APPEARANCE
    ATERRA7 ANTIBACTERIAL FOAMING HAND  FRAGRANCE FREE
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-117
    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
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    Colorwhite (water white, colorless - dispensed as white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68306-117-013785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/21/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/21/2024
    Labeler - B4 Ventures LLC (133582853)