Label: HEALTH SMART ANTIBACTERIAL HAND LAVENDER CHAMOMILE- chloroxylenol liquid

  • NDC Code(s): 52862-602-07
  • Packager: International Wholesale Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 14, 2023

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  • Drug Facts

  • Active Ingredient

    Chloroxylenol 0.3%

    Purpose

    Antibacterial

  • Uses

    for hand washing to help eliminate bacteria on the skin.

  • Warnings

    for external use only.

    When using this product:

    avoid contact with eyes. In case of eye contact, flush with water.

    Stop use and ask a doctor if:

    irritation and redness develops.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • pump into hands
    • lather vigorously for at least 15 seconds
    • rinse and dry thoroughly.
  • Other Information:

    Store at room temperature.   

  • Inactive Ingredients:

    Water, Sodium Laureth ulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Sodium Chloride, Fragrance, Glycerin, Citric Acid, PEG-150 Distearate, Methylchloroisothiazolinone, Methylisothiazolinone, D&C Red No.33, FD&C Blue No.1

  • Package Labeling

    label2

  • INGREDIENTS AND APPEARANCE
    HEALTH SMART ANTIBACTERIAL HAND LAVENDER CHAMOMILE 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52862-602
    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)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52862-602-07221 mL in 1 BOTTLE; Type 0: Not a Combination Product06/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/22/2020
    Labeler - International Wholesale Inc (161872676)
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