Virkon Tablets (Canada)
This page contains information on Virkon Tablets for veterinary use.The information provided typically includes the following:
- Virkon Tablets Indications
- Warnings and cautions for Virkon Tablets
- Direction and dosage information for Virkon Tablets
Virkon Tablets
This treatment applies to the following species:Soluble Effervescent Tablets
Disinfectant/Cleaner
Virucide Bactericide Fungicide Deodorant
READ THE LABEL AND LEAFLET BEFORE USING
KEEP OUT OF REACH OF CHILDREN
Broad spectrum germicide for cleaning and disinfection in veterinary hospitals, animal shelters, and of non-critical medical devices.
GUARANTEE/ACTIVE INGREDIENT:
Potassium monopersulphate |
21.4% W/W |
DIN 02253917
Description
Virkon™ is a disinfectant, possessing wide spectrum virucidal (Table 2), bactericidal (Table 3) and fungicidal (Table 4) activity. The effectiveness of Virkon™ is further enhanced by its excellent detergent properties, so that clean disease-free surfaces can be achieved. Virkon™ is unique in its composition. Its activity is based on a buffered synergized acid peroxygen system containing a high percentage of surfactant. Virkon™ is of low toxicity, non-tainting, and non-irritant. Because of its high detergency and mode of action, Virkon™ can be used in an exceptional variety of situations for effective cleaning and virucidal disinfection in a single operation. Virkon™ can be applied manually or through all types of cleaning and spraying equipment. The readily soluble effervescent tablet fully dissolve in lukewarm water in 3 to 4 minutes giving a clear pink solution. Virkon™ consists mainly of inorganic salts.
Detergent Sanitizer:
Virkon™ passes the AOAC germicidal and detergent sanitizer test at a concentration of 0.5% (1:200).
Directions for General Use:
Caution: animals must be removed from the immediate area during disinfection.
For cleaning and disinfection of surfaces, equipments and non-critical medical devices:
Remove heavy soil deposits then thoroughly wet surfaces to be disinfected with a 1% W/V solution of Virkon™, using a mop, sponge or cloth, as well as by spraying. A minimum contact time of 10 minutes is required. For laboratory equipment and bowls, scrub heavily soiled instruments or utensils and soak in a 1% W/V solution of Virkon™ for a minimum of 10 minutes (do not exceed 30 minutes for metal objects). For delicate medical devices (i.e. stethoscope, etc.), remove all organic material by cleaning and then thoroughly spray the device with a 1% W/V solution of Virkon™ and allow 10 minutes of contact time before wiping. Rinse with potable water equipment to be in contact with food.
Do not re-use a solution in which contaminated material has been soaked. The solution is stable for 7 days at room temperature.
IMPORTANT NOTE: In animal premises where there has been a disease outbreak and/or the mortality/morbidity rates are higher than normal and the causative agent has been determined by a pathology laboratory to be one of those listed in Table 1, the contact time/dilution rate indicated should be used.
For a complete listing of microorganisms against which Virkon™ is effective, refer to the Efficacy Charts 2, 3, and 4.
Dilution Instructions
Dilution Rate Required (W/V) |
Quantity of Disinfectant Solution Required |
|||
3.0 % |
2.0 % |
1.0 % |
0.5 % |
|
Quantity of Virkon™ Required |
||||
3 tabs |
2 tabs |
1 tab |
|
500 mL |
6 tabs |
4 tabs |
2 tabs |
1 tab |
1 Litre |
12 tabs |
8 tabs |
4 tabs |
2 tabs |
2 Litres |
1. Select the quantity of disinfectant solution required. 2. Choose appropriate dilution rate. 3. Add the number or Virkon™ Tablets to warm water.
Precautions
Keep out of reach of children. May be harmful if swallowed. Do not mix with other chemicals.
Storage
Store between 15°C and 25°C in a dry place in tightly sealed containers. The pack contains a desiccant sachet which must be retained during storage.
Presentation
Jar of 50 tablets of 5 grams each.
Table 1: Microorganisms for which a dilution rate of Virkon™ 0.5 to 3% W/V or a contact time > 10 minutes are required.
Microorganism |
Effective Dilution |
Contact Time Required (min.) |
Test Method |
Aspergillus fumigatus |
3% |
10 |
AOAC Fungicidal Test |
Bovine Papilloma Virus |
1% |
30 |
VLA, UK Method |
Dermatophilus congolensis |
2% |
10 |
AOAC Use Dilution Test |
Fusarium moniloforme |
2% |
10 |
AOAC* |
PRRS Virus |
0.5% |
30 |
VLA, UK Method |
Salmonella enteritidis |
2% |
10 |
AOAC Use Dilution Test |
Trichophyton mentagrophytes |
2% |
10 |
AOAC* |
* Modification of AOAC Fungicidal Test
Table 2: Viruses for which a 1% W/V dilution rate of Virkon™ and a contact time of 10 minutes are known to be effective.
Viruses |
Effective Dilution |
Contact Time |
Test Method |
Avian Infectious Bronchitis Virus |
1% |
10 |
AOAC* |
Avian Influenza Virus |
1% |
10 |
AOAC* |
Avian Laryngotracheitis Virus |
1% |
10 |
AOAC* |
Bovine Adenovirus Type 4 |
1% |
10 |
EPA Method |
Bovine Viral Diarrhea (BVD) Pestivirus |
1% |
10 |
EPA Method |
Calf Rotavirus |
1% |
10 |
EPA Method |
Canine Parvovirus |
1% |
10 |
EPA Method |
Duck Adenovirus |
1% |
10 |
EPA Method |
Equine Arteritis Virus |
1% |
10 |
EPA Method |
Equine Herpes Virus Type 1 |
1% |
10 |
EPA Method |
Equine Herpes Virus Type 3 |
1% |
10 |
EPA Method |
Equine Influenza Virus Type A |
1% |
10 |
EPA Method |
Feline Calicivirus |
1% |
10 |
EPA Method |
Feline Panleukopenia Virus |
1% |
10 |
EPA Method |
Feline Rhinotracheitis Virus |
1% |
10 |
EPA Method |
Infectious Bovine Rhinotracheitis Virus |
1% |
10 |
EPA Method |
Infectious Bronchitis Virus |
1% |
10 |
AOAC* |
Infectious Bursal Disease (Gumboro) Virus |
1% |
10 |
AOAC* |
Infectious Canine Hepatitis Adenovirus |
1% |
10 |
EPA Method |
Newcastle Disease Virus |
1% |
10 |
AOAC* |
Parainfluenza Virus |
1% |
10 |
EPA Method |
Parvovirus |
1% |
10 |
EPA Method |
Pseudorabies Virus |
1% |
10 |
EPA Method |
Simian Virus 40 (SV40) |
1% |
10 |
EPA Method |
TGE-Coronavirus |
1% |
10 |
EPA Method |
Turkey Herpes Virus |
1% |
10 |
EPA Method |
* Modification of AOAC Germicidal Spray Test
Table 3: Bacteria for which a 1% W/V dilution rate of Virkon™ and a contact time of 10 minutes are known to be effective.
Bacteria |
Effective Dilution |
Contact Time |
Test Method |
Actinobacillus pleuropneumoniae |
1% |
10 |
AOAC* |
Bordetella avium (Alcaligenes faecalis) |
1% |
10 |
AOAC Use Dilution Test |
Bordetella bronchiseptica |
1% |
10 |
AOAC Use Dilution Test |
Brucella abortus |
1% |
10 |
AOAC Use Dilution Test |
Helicobacter pylori (Campylobacter pyloridis) |
1% |
10 |
AOAC Use Dilution Test |
Campylobacter jejuni |
1% |
10 |
AOAC* |
Chlamydia psittaci |
1% |
10 |
EPA Method |
Erysipelothrix rhusiopathiae |
1% |
10 |
AOAC Use Dilution Test |
Escherichia coli |
1% |
10 |
AOAC Use Dilution Test |
Haemophilus somnus |
1% |
10 |
AOAC Use Dilution Test |
Klebsiella pneumoniae |
1% |
10 |
AOAC Use Dilution Test |
Listeria monocytogenes |
1% |
10 |
AOAC Use Dilution Test |
Moraxella bovis |
1% |
10 |
AOAC Use Dilution Test |
Mycoplasma gallisepticum |
1% |
10 |
AOAC Use Dilution Test |
Pasteurella haemolytica |
1% |
10 |
AOAC Use Dilution Test |
Pasteurella multocida |
1% |
10 |
AOAC Use Dilution Test |
Pseudomonas aeruginosa |
1% |
10 |
AOAC Use Dilution Test |
Salmonella choleraesuis |
1% |
10 |
AOAC Use Dilution Test |
Salmonella typhimurium |
1% |
10 |
AOAC Use Dilution Test |
Serpulina (Treponema) hyodysenteriae |
1% |
10 |
AOAC Use Dilution Test |
Shigella sonnei |
1% |
10 |
AOAC Use Dilution Test |
Staphylococcus aureus |
1% |
10 |
AOAC Use Dilution Test |
Staphylococcus epidermidis |
1% |
10 |
AOAC Use Dilution Test |
Streptococcus equi |
1% |
10 |
AOAC Use Dilution Test |
Streptococcus suis |
1% |
10 |
AOAC Use Dilution Test |
Haemophilus (Taylorella) equigenitalis |
1% |
10 |
AOAC Use Dilution Test |
* Modification of the AOAC Use Dilution Test
Table 4: Fungi for which a maximum 1% W/V dilution rate of Virkon™ and a contact time of 10 minutes are known to be effective.
Fungi |
Effective Dilution |
Contact Time Required (min.) |
Test Method |
Candida albicans |
1% |
10 |
AOAC Use Dilution Test |
Microsporum canis |
0.5% |
10 |
MHW Guideline, Japan |
Trichophyton verrucosum |
0.5% |
10 |
MHW Guideline, Japan |
* Modification of AOAC Fungicidal Test
ANTEC INTERNATIONAL LIMITED, Windham Road, Chilton Industrial Estate, Sudbury, Suffolk CO10 2XD UK
Tel.: + 44 (0) 1787 377305
Fax: + 44 (0) 1787 310846
Manufactured for: Vetoquinol N.-A. Inc., 2000, ch. Georges, Lavaltrie, QC, Canada J5T 3S5
Distributed by: Vetoquinol N.-A. Inc., 2000, ch. Georges, Lavaltrie, QC, Canada J5T 3S5
©2017 LANXESS. VIRKON™, LANXESS™, the LANXESS Logo and any associated logos are trademarks or copyrights of LANXESS Deutschland GmbH or its affiliates. All trademarks are registered in many countries worldwide.
Code 25390A
NET |
Code |
|
12 x 50 Tablets |
11834 |
A00964692/Virk/IFU/Vetoquinol,Canada/23.05.17/G A00960829/VirkST/12x50x5g/Vetoquinol,Canada/17.06.17/G |
CPN: 1234169.6
Commercial Division
2000, CHEMIN GEORGES, LAVALTRIE, QC, J5T 3S5
Telephone: | 450-586-2252 | |
Order Desk: | 800-363-1700 | |
Fax: | 450-586-4649 | |
Website: | www.vetoquinol.ca | |
Email: | info@vetoquinol.ca |
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Every effort has been made to ensure the accuracy of the Virkon Tablets information published above. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the Canadian product label or package insert. |
Copyright © 2021 Animalytix LLC. Updated: 2020-12-31