Label: INODERM CHOICE ANTIBACTERIAL- chloroxylenol liquid

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

Drug Label Information

Updated October 28, 2023

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  • Drug Facts

  • Active ingredient

    Chloroxylenol 0.3% w/w

    Purpose

    Antiseptic

  • Uses

    • Handwash to decrease bacteria on the skin that potentially can cause disease.
    • Recommended for repeated use.
  • Warnings

    For external use only

    When using this product

    keep away from eyes. In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if 

    irritation or redness develop or if 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 with water and dispense small amount of product into cupped palm of hand.
    • Lather vigorously for at least 15 seconds.
    • Rinse with water and dry thoroughly.
  • Inactive ingredients

    Water, Sodium Lauryl Ether Sulfate, Sodium Chloride, Cocamide MIPA, Sodium Sulfate, Fragrance, Magnesium Nitrate, Citric Acid, FD&C Yellow # 5, Methylchloroisothiazolinone, Magnesium Chloride, Methylsothiazolinone, FD&C Red # 4

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    INODERM CHOICE ANTIBACTERIAL 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73062-523
    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)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73062-523-423800 mL in 1 BOTTLE; Type 0: Not a Combination Product04/14/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/14/2023
    Labeler - Avro Enterprises LLC (804030166)
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