ZYLAST ANTISEPTIC- ethyl alcohol liquid 
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
Drug Facts

Active Ingredients

Ethyl alcohol 76%

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, Polyaminopropyl Biguanide, Panthenol, Hydroxyethyl Ethylcellulose, Farnesol, PEG- 12 Dimethicone, Benzethonium Chloride. 

Active Ingredients

Ethyl alcohol 76%

Purpose

Antiseptic

Uses

Warnings

Directions

Other Information

Inactive Ingredients

Water, Polyaminopropyl Biguanide, Panthenol, Hydroxyethyl Ethylcellulose, Farnesol, PEG- 12 Dimethicone, Benzethonium Chloride. 

Package/Label Principal Display Panel

NDC 57702-464-00
Zylast
Broad Spectrum
Antimicrobial
Antiseptic
2 fl oz/ 59.1 mL

NDC 57702-464-00 Zylast Broad Spectrum Antimicrobial Antiseptic 2 fl oz/ 59.1 mL

Package/Label Principal Display Panel

NDC 57702-464-03
Zylast
Broad Spectrum
Antimicrobial
Antiseptic
8 fl oz 236.6 mL

Zylast Broad Spectrum Antimicrobial Antiseptic 8 fl oz 236.6 mL

Package/Label Principal Display Panel

NDC 57702-464-13
Zylast
Broad Spectrum
Antimicrobial
Antiseptic
1000mL (33.8oz)

NDC 57702-464-13 Zylast Broad Spectrum Antimicrobial Antiseptic 1000mL (33.8oz)
ZYLAST ANTISEPTIC 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57702-464
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.76 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
FARNESOL (UNII: EB41QIU6JL)  
WATER (UNII: 059QF0KO0R)  
POLIHEXANIDE (UNII: 322U039GMF)  
PANTHENOL (UNII: WV9CM0O67Z)  
BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57702-464-0059.1 mL in 1 BOTTLE
2NDC:57702-464-03236.6 mL in 1 BOTTLE
3NDC:57702-464-131000 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
Document Id: 14f30d68-789e-40d2-aacd-cb9f8556cc2d
Set id: dbaf3296-49d4-472a-909b-df46556095af
Version: 3
Effective Time: 20140313
 
Bocchi Laboratories Inc.