ULTRA (CHLOROXYLENOL 0.3%) LIQUID [DOLGENCORP, LLC]

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ULTRA (CHLOROXYLENOL 0.3%) LIQUID [DOLGENCORP, LLC]
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NDC 55910-589-44
Set ID 1491d2c6-8b21-4d52-ade6-aad00afa47c1
Category HUMAN OTC DRUG LABEL
Packager Old East Main Co
Generic Name
Product Class
Product Number
Application Number PART333A
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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, sodium laureth sulfate, sodium lauryl sulfate, sodium xylenesulfonate, sodium chloride, 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

    When compared to non-concentrated formulas

    This product is not manufactured or distributed by Procter & Gamble,

    distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom

    DISTRIBUTED BY OLD EAST MAIN CO.

    100 MISSION RIDGE

    GOODLETTSVILLE, TN 37072

  • principal display panel

    ULTRA CONCENTRATED 3X CLEANING POWER

    trueliving

    Ultra

    Antibacterial

    Hand Soap

    Dishwashing Liquid

    TOUGH ON GREASE

    Compare to Dawn Ultra Antibacterial

    Hand Soap Apple Blossom Scent

    CRISP GREEN APPLE

    40 FL OZ (1.18 L)

    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) CHLOROXYLENOL3.09 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 XYLENESULFONATE (UNII: G4LZF950UR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    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:55910-589-44709 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
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/17/2017
    Labeler - Old East Main Co (068331990)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(55910-589)
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