Label: ZEST ANTIBACTERIAL LIQUID HAND LEMON PEEL- benzalkonium chloride soap

  • 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 December 16, 2020

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  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • USE

    For handwashing to decrease bacteria on the skin.

  • Warnings

    FOR EXTERNAL USE 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/Aqua/Eau, Cetrimonium Chloride, Glycerin, Cocamide MEA, Lauramidopropylamine Oxide, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Myristamidopropylamine Oxide, Citric Acid, Fragrance/Parfum, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Agastache Mexicana Flower/Leaf/Stem Extract, Citrus Limon (Lemon) Peel Extract, Coffea Arabica (Coffee) Seed Extract, Coffea Robusta Seed Extract, Malpighia Glabra (Acerola) Fruit Extract, Glycolic Acid, Malic Acid, Yellow 5 (CI 19140), Yellow 6 (CI 15985)

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Zest Antibacterial Soap_Lemon_70pct EtOH_11.25oz

  • INGREDIENTS AND APPEARANCE
    ZEST ANTIBACTERIAL LIQUID HAND  LEMON PEEL
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81277-103
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Glycerin (UNII: PDC6A3C0OX)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    Lauramidopropylamine Oxide (UNII: I6KX160QTV)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    AGASTACHE FOENICULUM WHOLE (UNII: ZV7TA06J2V)  
    AGAVE TEQUILANA LEAF (UNII: 05545M0E3M)  
    LEMON PEEL (UNII: 72O054U628)  
    ARABICA COFFEE BEAN (UNII: 3SW678MX72)  
    ROBUSTA COFFEE BEAN (UNII: V5032728L7)  
    ACEROLA (UNII: XDD2WEC9L5)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    MALIC ACID (UNII: 817L1N4CKP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81277-103-11332 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E12/16/2020
    Labeler - TCP HRB HOLDINGS LLC (117465959)
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