Label: ULTRA- 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 April 7, 2022

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  • 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 and/or lauramidopropylamine oxide and myristamidopropylamine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, sodium xylenesulfonate, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, tetrasodium EDTA, yellow 5, blue 1

  • SPL UNCLASSIFIED SECTION

    WARNING

    NOT FOR USE IN DISHWASHERS.

    DO NOT ADD BLEACH

    Phosphate Free Contains Surfactants

    Not tested on animals

    ANTIBACTERIAL

    HAND SOAP

    GREEN APPLE SCENT

    Ultra Concentrated

    Dishwashing Liquid

    DIST. & SOLD EXCLUSIVELY BY:

    ALDI, BATAVIA, IL 60510

    This product is not manufactured or distributd by Procter & Gamble,  distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom Scent

  • principal display panel

    Radiance

    TOUCH ON GREASE

    ANTIBACTERIAL | HAND SOAP

    COMPARE TO DAWN ULTRA ANTIBACTERIAL HAND SOAP APPLE BLOSSOM SCENT

    24 FL OZ (710 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ULTRA 
    chloroxylenol 0.3% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64024-956
    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)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    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 MONOHYDRATE (UNII: 2968PHW8QP)  
    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:64024-956-50710 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/17/2019
    Labeler - Aldi (944259522)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(64024-956)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(64024-956)
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