Label: CLOROX CARE CONCEPTS 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 November 14, 2014

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

  • Active ingredient

    Benzalkonium chloride 0.12%

  • Purpose

    Antiseptic handwash

  • Use

    • For handwashing to decrease bacteria on skin that potentially can cause disease
    • Recommended for repeated use
  • Warnings

    For external use only.

  • WHEN USING

    When using this product, do not use in the eyes.

  • STOP USE

    Discontinue use and ask a doctor if

    • irritate and redness develop.
    • condition persists for more than 72 hours.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • Wet hands and forearms.
    • Dispense onto hands.
    • Scrub thoroughly for 30 seconds.
    • Rinse and repeat.
  • Inactive ingredients

    Benzyl Alcohol, Citric Acid, Cocamidopropyl Betaine, Dehydroacetic Acid, Glycerin, Phenoxyethanol, Poloxamer 124, Sodium Hydroxide, Tetra Sodium EDTA, Water

  • PRINCIPAL DISPLAY PANEL

    HandSoapLabel

    Clorox Care Concepts

    Antimicrobial Soap

  • INGREDIENTS AND APPEARANCE
    CLOROX CARE CONCEPTS ANTIMICROBIAL 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.12 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLOXAMER 124 (UNII: 1S66E28KXA)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:26509-0003-144 mL in 1 BOTTLE, PUMP
    2NDC:26509-0003-2249 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/2014
    Labeler - The Clorox Company (009138033)
    Registrant - The Clorox Company (009138033)