ZYLAST XP ANTISEPTIC FOAMING- benzethonium chloride soap 
Bocchi Laboratories Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Zylast Antiseptic Foaming Soap
Drug Facts

Active Ingredients

Benzethonium Chloride - 0.20%

Purpose

Antiseptic

Uses

Warnings

Keep out of reach of children.

 If swallowed, immediately call Poison Control Center or doctor.

Directions

Other Inforamtion

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

Warnings

Directions

Other Information

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)

ZYLAST XP ANTISEPTIC FOAMING 
benzethonium chloride soap
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:57702-487
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 2 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
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 Code Package Description Marketing Start Date Marketing End Date
1 NDC:57702-487-05 244 mL in 1 BOTTLE
2 NDC:57702-487-15 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)

Revised: 3/2014
Document Id: 4d8bdc3d-7ff7-4c87-a8cd-ec1ef25408da
Set id: edeaa363-f3d7-4dac-a3a9-e371f05e3322
Version: 5
Effective Time: 20140331
 
Bocchi Laboratories Inc.