VANQUISH PRE-POST BASE - sodium chlorite solution 
DeLaval Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Vanquish PrePost Base

Vanquish Pre Post

Sanitizing Pre and Post Teat Dip
Disinfectante pre y post ordeno

ACTIVE INGREDIENTS:

Sodium Chlorite .................. 0.56%

BASE - For use with only Vanquish PrePost Activator

1013-B0809

KEEP OUT OF REACH OF CHILDREN

! CAUTION

MANTENER FUERA DEL ALCANCE DE LOS NINOS

! CUIDADO

SI USTED NO PUEDE LEER ESTA ETIQUETA, POR FAVOR PIDA A ALGUIEN MAS QUE SE LA LEA ANTES DE USAR ESTE PRODUCTO

READ AND UNDERSTAND ALL INSTRUCTIONS BEFORE USING THIS PRODUCT

Not For Human Use

Additional Information on Material Safety Data Sheet

USE DIRECTIONS
MIXING INSTRUCTIONS

GENERAL INSTRUCTIONS PRE-DIPPING POST-DIPPING

STORAGE AND DISPOSAL

FIRST AID
Contact with product can cause irritation to eyes and skin. Avoid contact with eyes and skin.

If On Skin: Flush affected area with water. Remove contaminated clothing and shoes. Get medical attention if irritation develops.

Eye Contact: Flush with water. Remove contact lenses, if present, after first 5 minutes. Then continue rinsing. Get immediate medical attention.

If Swallowed: Do not induce vomiting. If victim is fully conscious, give a cupful of water. Never give anything by mouth to an unconscious person. Get immediate medical attention.

CHEMTREC EMERGENCY NUMBER
1-800-424-9300

Manufactured for:
DeLaval
Kansas City, MO 64153

Copyright 2007, DeLavel
Made in U.S.A.

NET CONTENTS:

LOT NO.:

EXP. DATE:

 Product Container Label

VANQUISH PRE-POST BASE 
sodium chlorite solution
Product Information
Product TypeOTC ANIMAL DRUG LABELItem Code (Source)NDC:55756-013
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Chlorite (CHLORITE ION) Sodium Chlorite7.0 g  in 1 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55756-013-0818.9 L in 1 PAIL
2NDC:55756-013-0256.8 L in 1 DRUM
3NDC:55756-013-01208.2 L in 1 DRUM
4NDC:55756-013-271040.9 L in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/21/2012
Labeler - DeLaval Inc. (173704867)
Registrant - West Agro, Inc. (069288728)
Establishment
NameAddressID/FEIBusiness Operations
West Agro, Inc.147528723manufacture, api manufacture, analysis, label, pack
Establishment
NameAddressID/FEIBusiness Operations
K Klean dba West Agro, Inc.002222368manufacture, analysis, api manufacture, label, pack
Establishment
NameAddressID/FEIBusiness Operations
West Agro, Inc.044610140manufacture, analysis, api manufacture, label, pack

Revised: 5/2013
Document Id: ccab6504-c718-41a3-b5b1-10d7734d8d66
Set id: 7d2599a2-dd19-43f2-a2f1-57be1bf23580
Version: 7
Effective Time: 20130507
 
DeLaval Inc.