Label: CLOROX ANTIMICROBIAL- 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 February 2, 2023

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  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Use

    • For handwashing to decrease bacteria on skin
  • Warnings

    For external use only.

    In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water. If irritation persists, contact a Poison Control Center right away.

    Keep out of reach of children.

  • Directions

    • Apply onto wet hands, lather for 30 seconds and rinse thoroughly.
  • Other Information

    • Avoid freezing and excessive heat above 40℃ (104℉).
  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Sodium Chlroride, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Laureth-3, Sodium Bicarbonate, Disodium EDTA, Fragrance, Methylchloroisothiazolinone, Methylisothiazoline, Blue 1 (Ci 42090), Red 33 (Ci 17200).

  • SPL UNCLASSIFIED SECTION

    Do not add bleach.

    Not for use in dishwashers.

    PHOSPATE-FREE

    BLEACH-FREE

    Distributed by: Brand Buzz LLC., 1407 Broadway, New York, NY 10018

    Clorox and logo are registered trademarks of the Clorox Company and are used under license by Brand Buzz LLC.
    All Rights Reserved.

  • Questions or Comments?

    Visit us at www.brandbuzzcp.com or call us at: 1-888-508-4750

    For more product ingredient information, visit www.brandbuzzcp.com/ingredients

  • PRINCIPAL DISPLAY PANEL

    Clorox

    Antimicrobial

    HandSoap

    Ultra Concentrated Dishwashing Liquid

    Lavender Scent

    with Oxi

    Bleach-Free

    8FL OZ

    (0.5 PT) 236 mL

    Label

    Label

  • INGREDIENTS AND APPEARANCE
    CLOROX ANTIMICROBIAL 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69540-0031
    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
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    C12-14 PARETH-12 (UNII: M0LJS773XW)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorFRUIT (Lavender) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69540-0031-1650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/2014
    Labeler - Brand Buzz LLC (079266204)
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