Label: PURELOGIC EUCALYPTUS ANTIBACTERIAL HAND- chloroxylenol soap

  • 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 September 1, 2020

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  • Active Ingredient(s)

    Chloroxylenol 0.2%

  • PURPOSE

    Purpose: 

    Antibacterial

  • Use

    Helps eliminate bacteria on hands

  • Warnings

    For external use only

  • When using this product

    When using this product, avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water

  • Stop use and ask a doctor

    if redness and irrigation develop and last

  • Keep out of reach of children

    if swallowed, get medical help or contact a Poison Control Center immediately

  • Directions

    Apply onto wet hands. Lather and rinse thoroughly

  • Other information

    Store at room temperature

  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Cocamide DEA, Citric Acid, Phenoxyethanol, Fragrance, Cocamidopropyl betaine, Disodium EDTA,  Blue 1 (CI42090)

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    PURELOGIC EUCALYPTUS ANTIBACTERIAL HAND 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77731-061
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DISODIUM HEDTA (UNII: KME849MC7A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77731-061-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/01/2020
    Labeler - Argento sc by sicura inc. (168718778)
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