Label: CHLOROXYLENOL 0.30 %- chloroxylenol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 15, 2025

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  • Active ingredient

    Chloroxylenol 0.30 %

  • Purpose

    Antibacterial

  • Use

    for hand washing to decrease bacteria on the skin.

  • Warnings

    For external use only

  • WHEN USING

    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 and redness develops
    • condition persists for more than 72 hours
  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. If product gets in eye, flush thoroughly with water. In case of accidental ingestion, drink a glass of water to dilute.

  • Directions

    Wet hands and forearms. Apply palmful to hands and forearms. Scrub thoroughly for 30 seconds and rinse.

  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Lauramine Oxide, Sodium Xylenesulfonate, Citric Acid, Methylisothiazolinone, Methylchloroisothiazolinone,
    Fragrance, Sodium Chloride, Yellow 5, Blue 1.

  • NDC 42669-028-03

    L-D36612 LABTGT0005F-1 Target Up&Up Dish Soap 28 oz FRONT_page-0001

  • PRINCIPAL DISPLAY PANEL

    L-D36613 LABTGT0005B-1 Target Up&Up Dish Soap 28 oz BACK__page-0001

  • INGREDIENTS AND APPEARANCE
    CHLOROXYLENOL 0.30 % 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42669-028
    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 LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42669-028-03828 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/15/2025
    Labeler - Davion, Inc (174542928)
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