Label: ZYLAST XP ANTISEPTIC- benzethonium chloride lotion 

  • Label RSS
  • NDC Code(s): 57702-465-01, 57702-465-04, 57702-465-14
  • Packager: Bocchi Laboratories Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 03/14

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Benzethonium Chloride - 0.20%

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  • Purpose

    Antiseptic

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  • Uses

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

    • For external use only.
    • Avoid contact with eyes. In case of eye contact, rinse 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.
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  • Directions

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

    • Store at 20-25°C (68-77°F)
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  • Inactive ingredients

    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.

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  • Active Ingrdients

    Benzethonium Chloride - 0.20%

    Close
  • Purpose

    Antiseptic

    Close
  • Uses

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

    • For external use only.
    • Avoid contact with eyes. In case of eye contact, rinse 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.
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  • Keep out of reach of children.

     If swallowed, immediately call Poison Control Center or doctor.

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  • Directions

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

    •  Store at 20-25°C (68-77°F)
    Close
  • Inactive Ingredients

    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.

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  • Package/Label Principal Display Panel

    NDC 57702-465-14
    Zylast XP
    Extended Protection
    Broad Spectrum
    Antimicrobial
    Antiseptic
    1000mL (33.8oz)

    NDC 57702-465-14 Zylast XP Extended Protection Broad Spectrum Antimicrobial Antiseptic 1000mL (33.8oz)
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  • Package/Label Principal Display Panel

    NDC 57702-465-04
    Zylast XP
    Extended Protection
    Broad Spectrum
    Antimicrobial
    Antiseptic
    8 fl oz. 236.6 mL

    NDC 57702-465-04 Zylast XP Extended Protection Broad Spectrum Antimicrobial Antiseptic 8 fl oz. 236.6 mL
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  • Package/Label Principal Display Panel

    NDC 57702-465-01
    Zylast XP
    Extended Protection
    Broad Spectrum
    Antimicrobial
    Antiseptic
    2 fl oz 59.1 mL

    NDC 57702-465-01 Zylast XP Extended Protection Broad Spectrum Antimicrobial Antiseptic 2 fl oz 59.1 mL
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  • INGREDIENTS AND APPEARANCE
    ZYLAST XP ANTISEPTIC 
    benzethonium chloride lotion
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:57702-465
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE 2 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    CETOSTEARYL ALCOHOL  
    GLYCERIN  
    POLIHEXANIDE  
    DIMETHICONE  
    STEARAMIDOPROPYL DIMETHYLAMINE  
    BENZYL ALCOHOL  
    FARNESOL  
    PANTHENOL  
    ZINC GLUCONATE  
    CHLORHEXIDINE GLUCONATE  
    CITRIC ACID MONOHYDRATE  
    .ALPHA.-TOCOPHEROL ACETATE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57702-465-01 59.1 mL in 1 BOTTLE
    2 NDC:57702-465-04 236.6 mL in 1 BOTTLE
    3 NDC:57702-465-14 1000 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333E 06/01/2011
    Labeler - Bocchi Laboratories Inc. (078376306)
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