Label: CHLOROXYLENOL 0.3% 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 January 29, 2021

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

  • Active ingredient

    Chloroxylenol 0.3%

  • Purpose

    Antibacterial

  • Use

     for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only: hands only

  • When using this product

    • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water
  • Stop use and ask a doctor if

    • irritation or redness develops
    • condition persists for more than 72 hours
  • Keep out of reach of children.

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

  • Directions

    • wet hands
    • apply palmful to hands
    • scrub thoroughly
    • rinse thoroughly
  • Inactive ingredients

    water, sodium C14-16 olefin sulfonate, lauramine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium xylenesulfonate, sodium chloride, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, yellow 5, blue 1

  • principal display panel

    COMPARE TO DAWN ULTRA ANTIBACTERIAL HAND SOAP

    Total

    Home

    Antibacterial HAND SOAP

    GREEN APPLE

    Ultra Concentrated

    Tough on Grease

    Phosphate-Free Formula

    40 FL OZ (1.18 L)

    image description

  • INGREDIENTS AND APPEARANCE
    CHLOROXYLENOL 0.3% 
    chloroxylenol 0.3% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-946
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3.09 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    ALCOHOL (UNII: 3K9958V90M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CITRIC ACID ACETATE (UNII: DSO12WL7AU)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-946-571180 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/17/2017
    Labeler - CVS Pharmacy (062312574)
    Registrant - Vi-Jon, LLC (088520668)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(69842-946)