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

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ZYLAST XP ANTISEPTIC FOAMING (BENZETHONIUM CHLORIDE) SOAP [BOCCHI LABORATORIES INC.]
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NDC 57702-487-05, 57702-487-15
Set ID edeaa363-f3d7-4dac-a3a9-e371f05e3322
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.
  • Keep out of reach of children.

     If swallowed, immediately call Poison Control Center or doctor.

  • Directions

    • Wet hands and forearms. Apply a palmful to hands and scrub hands and forearms thoroughly for 15 seconds or more. Rinse and repeat.
  • Other Inforamtion

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

    Water, Alcohol Denat., Lauramine Oxide, Cocamidopropyl Betaine, Cetrimonium Chloride, Butylene Glycol, Citric Acid, Zinc Gluconate, PPG-2 Hydroxyethyl Cocamide, Farnesol, Glycerin, Methylchloroisothiazolinone, Polyaminopropyl Biguanide, Fragrance, Polyquaternium-10.

  • 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 and forearms. Apply a palmful to hands and scrub hands and forearms thoroughly for 15 seconds or more. Rinse and repeat.

  • Other Information

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

    Water, Alcohol Denat., Lauramine Oxide, Cocamidopropyl Betaine, Cetrimonium Chloride, Butylene Glycol, Citric Acid, Zinc Gluconate, PPG-2 Hydroxyethyl Cocamide, Farnesol, Glycerin, Methylchloroisothiazolinone, Polyaminopropyl Biguanide, Fragrance, Polyquaternium-10.

  • Package/Label Principal Display Panel

    NDC 57702-487-05
    Zylast XP
    Extended Protection
    Broad Spectrum
    Antimicrobial
    Antiseptic
    Foaming Soap
    8.25 oz 244mLNDC 57702-487-05 Zylast XP Extended Protection Broad Spectrum Antimicrobial Antiseptic Foaming Soap 8.25 oz 244mL

  • Package/Label Principal Display Panel

    NDC 57702-487-15
    Zylast XP
    Extended Protection
    Broad Spectrum
    Antimicrobial
    Antiseptic
    Foaming Soap
    1000mL (33.8oz)

     NDC 57702-487-15 Zylast XP Extended Protection Broad Spectrum Antimicrobial Antiseptic Foaming Soap 1000mL (33.8oz)

  • INGREDIENTS AND APPEARANCE
    ZYLAST XP ANTISEPTIC FOAMING 
    benzethonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57702-487
    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)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    FARNESOL (UNII: EB41QIU6JL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    POLIHEXANIDE (UNII: 322U039GMF)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57702-487-05244 mL in 1 BOTTLE
    2NDC:57702-487-151000 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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