Label: ULTRA- chloroxylenol 0.3% liquid

  • NDC Code(s): 55910-589-38, 55910-589-44, 55910-589-57, 55910-589-68
  • Packager: Old East Main Co
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 11, 2024

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  • Disclaimer

    Do not add bleach.

    Not for use in dishwasher.

    Contains Surfactants

    *This product is not manufactured or distributed by Proctor & Gamble, distributor of Dawn ® Ultra Antibacterial Hand Soap Apple Blossom ® Scent.

    **when compared to non-concentrated formulas

  • Adverse reaction

    100% Satisfaction Guarnateed! (888)309-9030

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

  • Adverse reaction

    DISTRIBUTED BY OLD EAT MAIN CO.

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

  • Principal display panel

    ULTRA CONCENTRATED 3X CLEANING POWER**

    truekiving

    Ultra Antibacterial Hand Soap

    Dishwashing Liquid

    TOUGH ON GREASE

    Compare to Dawn Ultra Antibacterial Hand Soap Apple Blossom Scent*

    CRISP GREEN APPLE

    image description

  • INGREDIENTS AND APPEARANCE
    ULTRA 
    chloroxylenol 0.3% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-589
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3 mg  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 CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    ALCOHOL (UNII: 3K9958V90M)  
    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:55910-589-44532 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2017
    2NDC:55910-589-571183 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2017
    3NDC:55910-589-681656 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product01/17/2017
    4NDC:55910-589-381124 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 Drug505G(a)(3)01/17/2017
    Labeler - Old East Main Co (068331990)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(55910-589)
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