Label: ZYLASTXP ANTISEPTIC- benzethonium chloride lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated August 26, 2021

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  • ACTIVE INGREDIENT

    Benzethonium Chloride - 0.2%

  • PURPOSE

    Antiseptic

  • ASK DOCTOR

    Discontinue use of irritation and redness develops. Consult a doctor if condition persists for more than 72 hours.

  • DOSAGE & ADMINISTRATION

    Wet hands thoroughly with product and allow to dry without wiping.

  • WARNINGS

    For external use only. Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water. Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours. If swallowed, immediately call Poison Control Center or doctor.

  • INACTIVE INGREDIENT

    Water, Alcohol Denat., Cetearyl Alcohol, Glycerin, Polyaminopropyl Biguanide, Dimethicone, Stearamidopropyl Dimethylamine, Benzyl Alcohol, Farnesol, Panthenol, Zinc Gluconate, Chlorhexidine Digluconate, Citric Acid, Polyquaternium-10, Tocopheryl Acetate.

  • INDICATIONS & USAGE

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

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, immediately call Poison Control Center or doctor.

  • PRINCIPAL DISPLAY PANEL

    NDC 57362-464-03

    Zylas Antiseptic Lotion 8oz

    Broad Spectrum

    Antimicrobial

    Fast Acting

    8oz. Lotion

  • INGREDIENTS AND APPEARANCE
    ZYLASTXP ANTISEPTIC 
    benzethonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57362-464
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE192.3 mg  in 1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57362-464-03227 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only04/24/2015
    Labeler - Innovative BioDefense (078363903)
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