Label: ZEST AQUA ANTIBACTERIAL HAND ZEST- benzalkonium chloride soap

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

Drug Label Information

Updated March 1, 2024

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only - hands only

    When using this product

    • avoid contact with the eyes. If contact occurs, rinse eyes with water.

    Stop use and ask a doctor if

    • irritation or redness develops.

    Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet hands
    • apply to palm of hand
    • scrub thoroughly
    • rinse thoroughly
  • Inactive ingredients

    Water, Cetrimonium Chloride, Glycerin, Cocamide MEA, Lauramidopropylamine Oxide, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Myristamidopropylamine Oxide, Citric Acid, Fragrance, Tetrasodium EDTA, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Methylchloroisothiazolinone, Green 3, Methylisothiazolinone.

  • SPL UNCLASSIFIED SECTION

    Distributed By: High Ridge Brands, LLC. Stamford, CT 06902.

  • PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label

    Clean Zestfully!

    Zest

    Antibacterial
    LIQUID HAND SOAP

    PLUS
    VITAMIN E
    & ALOE

    FRESH AQUA

    7.5 FL. OZ. (221 mL)

    12P8003

    PRINCIPAL DISPLAY PANEL - 221 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    ZEST AQUA ANTIBACTERIAL HAND  ZEST
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81277-179
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Product Characteristics
    Colorblue (Aqua Blue) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81277-179-41221 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/17/2020
    Labeler - TCP HRB Holdings (117465959)