ZYLAST XP ANTISEPTIC (BENZETHONIUM CHLORIDE) LOTION [BOCCHI LABORATORIES INC.]

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ZYLAST XP ANTISEPTIC (BENZETHONIUM CHLORIDE) LOTION [BOCCHI LABORATORIES INC.]
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NDC 57702-465-01, 57702-465-04, 57702-465-14
Set ID 6e4a94d3-ae02-406a-bee1-0d9d85ab6b93
Category HUMAN OTC DRUG LABEL
Packager Bocchi Laboratories Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Active Ingredients

    Benzethonium Chloride - 0.20%

  • Purpose

    Antiseptic

  • Uses

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

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

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

  • Active Ingrdients

    Benzethonium Chloride - 0.20%

  • Purpose

    Antiseptic

  • Uses

    • Handwash to decrease bacteria on the skin that potentially can cause disease.
    • Recommended for repeated use.
  • 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.
  • Keep out of reach of children.

     If swallowed, immediately call Poison Control Center or doctor.

  • Directions

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

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

  • 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)
  • 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
  • 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
  • INGREDIENTS AND APPEARANCE
    ZYLAST XP ANTISEPTIC 
    benzethonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57702-465
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLIHEXANIDE (UNII: 322U039GMF)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    FARNESOL (UNII: EB41QIU6JL)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57702-465-0159.1 mL in 1 BOTTLE
    2NDC:57702-465-04236.6 mL in 1 BOTTLE
    3NDC:57702-465-141000 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E06/01/2011
    Labeler - Bocchi Laboratories Inc. (078376306)
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