Label: KITCHEN LEMON ZEST- benzalkonium chloride liquid

  • 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 November 3, 2018

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients     Benzalkonium Chloride 0.13%

  • PURPOSE

    Purpose     Antibacterial

  • INDICATIONS & USAGE

    Uses  for hand washing to decrease bacteria on the skin.

  • WARNINGS

    Warnings  For external use only.

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor if irritation and redness develops.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions ■ pump into hands ■ lather vigorously for at
    least 15 seconds ■ rinse and dry thoroughly.

  • INACTIVE INGREDIENT

    Inactive ingredients Water, Sodium Laureth Sulfate,
    Cocamidopropyl Betaine, Glycerin, Sodium Lauryl Sulfate, PEG-150
    Distearate, Fragrance, Citric Acid, Methylchloroisothiazolinone,
    Methylisothiazolinone, FD&C Yellow No. 5, FD&C Red No. 40

  • Principal Display Package

    719 Walnut®

    Avenue

    KITCHEN
    LEMON ZEST

    Antibacterial

    Foaming Hand Soap

    12 FL OZ (354 mL)

    719 Walnut®

    Avenue

    KITCHEN
    LEMON ZEST

    Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716

    3-29500-00199-8

    Made in China

    ↓Product Package↓

    Kitchen Lemon Zest

                                   KITCHEN LEMON ZEST by Wal-Mart Stores, Inc.

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  • INGREDIENTS AND APPEARANCE
    KITCHEN LEMON ZEST 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9882
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.44 g  in 354 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:29500-9882-1354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/01/2018
    Labeler - GL 360 (966155082)
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