ZYLAST XP ANTISEPTIC- benzethonium chloride lotion 
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 Lotion
Drug Facts

Active Ingredients

Benzethonium Chloride - 0.20%

Purpose

Antiseptic

Uses

Warnings

Directions

Other Information

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

Warnings

Keep out of reach of children.

 If swallowed, immediately call Poison Control Center or doctor.

Directions

Other Information

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
ZYLAST XP ANTISEPTIC 
benzethonium chloride lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:57702-465
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)  
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 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)

Revised: 3/2014
Document Id: 514301b8-470b-47ff-b6ab-8c20e85f36ac
Set id: 6e4a94d3-ae02-406a-bee1-0d9d85ab6b93
Version: 6
Effective Time: 20140331
 
Bocchi Laboratories Inc.