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

Sanitizing pre and post teat dip
Aids in reducing the spread of mastitis-causing organisms

Sanitizante pre y post ordeno
Ayuda a reducir la transmision de microorganismos que causan mastitis

ACTIVE INGREDIENTS:

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

Base - For use with only Vanquish Pre Post ACTIVATOR

1013-D0514

KEEP OUT OF REACH OF CHILDREN

! CAUTION

MANTENER FUERA DEL ALCANCE DE LOS NINOS

! CUIDADO

1013

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

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.

STORAGE AND DISPOSAL
THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN. Avoid contact with food or feed. Avoid storing near heat or open flame. Keep container tightly closed when not in use. If product has frozen, thaw in a warm room and shake well before use. Do not reuse empty container. Rinse empty container before disposing of in a safe manner. Do not store near acids.

CHEM-TREC EMERGENCY NUMBER 1-800-424-9300

Not for Human Use

Additional Information on Material Safety Data Sheet

Product Label

VANQUISH PRE-POST BASE 
sodium chlorite solution
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:55756-013
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Sodium Chlorite (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) Sodium Chlorite 7.0 g  in 1 L
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55756-013-08 18.9 L in 1 PAIL
2 NDC:55756-013-02 56.8 L in 1 DRUM
3 NDC:55756-013-01 208.2 L in 1 DRUM
4 NDC:55756-013-27 1040.9 L in 1 DRUM
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/21/2012
Labeler - DeLaval Inc. (173704867)
Registrant - West Agro, Inc. (069288728)
Establishment
Name Address ID/FEI Business Operations
West Agro, Inc. 147528723 manufacture, api manufacture, analysis, label, pack
Establishment
Name Address ID/FEI Business Operations
K Klean dba West Agro, Inc. 002222368 manufacture, analysis, api manufacture, label, pack
Establishment
Name Address ID/FEI Business Operations
West Agro, Inc. 044610140 manufacture, analysis, api manufacture, label, pack

Revised: 4/2015
Document Id: f65c20a0-e079-4b37-8fe9-3b4378d49d4e
Set id: 7d2599a2-dd19-43f2-a2f1-57be1bf23580
Version: 10
Effective Time: 20150430
 
DeLaval Inc.