Your browser does not support JavaScript! ZYLAST XP ANTISEPTIC (BENZETHONIUM CHLORIDE) LOTION [BOCCHI LABORATORIES INC.]
DailyMed Logo Header image

Daily Med

Current Medication Information

Options

RxNorm Names

ZYLAST XP ANTISEPTIC (benzethonium chloride) lotion
[Bocchi Laboratories Inc.]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph not final
NOTE: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.
Drug Label Sections

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
ZYLAST XP ANTISEPTIC 
benzethonium chloride lotion
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:57702-465
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
CETOSTEARYL ALCOHOL 
GLYCERIN 
POLIHEXANIDE 
DIMETHICONE 
STEARAMIDOPROPYL DIMETHYLAMINE 
BENZYL ALCOHOL 
FARNESOL 
PANTHENOL 
ZINC GLUCONATE 
CHLORHEXIDINE GLUCONATE 
CITRIC ACID MONOHYDRATE 
.ALPHA.-TOCOPHEROL ACETATE 
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)

Revised: 3/2014
 
Bocchi Laboratories Inc.

Visit The National Library of Medicine Copyright, Privacy, Accessibility
U.S. National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20894
National Institutes of Health, Health & Human Services