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POM-VPS Prescription Required

Virbamec Super 10 mg/ml, 100 mg/ml Solution for Injection

Active ingredients: Clorsulon, Ivermectin

Form

Injection

Species

Cattle

Manufacturer

Virbac

VMD MA No.

05653/4155

What it's used for

For the treatment of mixed trematode and nematode or arthropod infestations, due to adult and immature roundworms, lungworms, warbles, mites, lice and live...

Full indications, dosage and side effects ↓
View official SPC (PDF)

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    The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.

Prescription required

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Clinical information

Virbamec Super 10 mg/ml, 100 mg/ml Solution for Injection — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.

For the treatment of mixed trematode and nematode or arthropod infestations,
due to adult and immature roundworms, lungworms, warbles, mites, lice and
liver fluke in cattle.
Gastro-intestinal roundworms (adult and fourth-stage larvae):
Ostertagia ostertagi
O. lyrata
Haemonchus placei
Trichostrongylus axei
Trichostrongylus colubriformis
Cooperia oncophora
Cooperia punctata
Cooperia pectinata
Bunostomum phlebotomum
Oesophagostomum radiatum

Revised: April 2024
AN: 01199/2023 & 01201/2023Page 2 of 7
Strongyloides papillosus (adult)
Nematodirus helvetianus (adult)
Nematodirus spathiger
Lungworms (adult and fourth-stage larvae):
Dictyocaulus viviparus
Liver fluke (adult):
Fasciola hepatica
Warbles (parasitic stages):
Hypoderma bovis
Hypoderma lineatum
Mange mites:
Psoroptes bovis
Sarcoptes scabiei var. bovis
Sucking lice:
Linognathus vituli
Haematopinus eurysternus
The product may also be used as an aid in the control of the mange mite
Chorioptes bovis, but complete elimination may not occur.
The product should be given once by subcutaneous injection at the
recommended dosage level of 200 µg of ivermectin and 2 mg of clorsulon per
kilogram of bodyweight. Each ml contains 10 mg of ivermectin and 100 mg of
clorsulon, sufficient to treat 50 kg of bodyweight. Subcutaneous injection only.
To ensure administration of a correct dose, bodyweight should be determined
as accurately as possible; accuracy of the dosing device should be checked.
If animals are to be treated collectively rather than individually they should be
grouped according to their bodyweight and dosed accordingly, in order to avoid
under- or over-dosing.
Divide doses greater than 10 ml between two injection sites.
Inject under the loose skin behind the shoulder. Use of a 17-gauge, ½-inch (15-
20 mm) needle is suggested. The injection may be given with any standard
automatic, multidose or single-dose hypodermic syringe. If using a hypodermic
syringe, use a separate sterile needle to withdraw the dose from the pack.
This product does not contain an antimicrobial preservative. Swab septum
before removing each dose. Use a dry, sterile needle and syringe.
For 200, 500 and 1000-ml pack sizes, use only automatic-syringe equipment.
Injection on animals with wet or dirty hides is not recommended.
When the temperature of the product is below 5 °C, difficulty in administration
may be encountered due to increased viscosity. Warming the product and
injection equipment to about 15 °C will greatly increase the ease with which the
product can be injected. Different injection sites should be used for other
parenteral products.
The timing for treatment should be based on epidemiological factors and should
be customised for each individual farm. A dosing programme should be
established by the veterinary surgeon.

Revised: April 2024
AN: 01199/2023 & 01201/2023Page 5 of 7
Do not use in non-lactating dairy cows including pregnant heifers within 60 days
of calving.
Not for use in species other than cattle as severe adverse reactions, including
fatalities, may occur in dogs for example.
Do not use by the intravenous or intramuscular route.
Do not use in animals known to be hypersensitive to the active substance.
Transitory discomfort has been observed in some cattle following subcutaneous
administration. Soft-tissue swelling and/or slight pain at the injection site has
also been observed. These reactions have disappeared without treatment. In
case of hypersensitivity reactions a symptomatic treatment should be applied
Care should be taken to avoid the following practices because they increase the
risk of development of resistance and could ultimately result in ineffective
therapy:
•
extended period of time.
•
misadministration of the product, or lack of calibration of the dosing device (if
any).

Revised: April 2024
AN: 01199/2023 & 01201/2023Page 3 of 7
Suspected clinical cases of resistance to anthelmintics should be further
investigated using appropriate tests (e.g. Faecal Egg Count Reduction Test).
Where the results of the test(s) strongly suggest resistance to a particular
anthelmintic, an anthelmintic belonging to another pharmacological class and
having a different mode of action should be used”.
Resistance to macrocyclic lactones (which includes ivermectin) has been
reported in , in cattle within the EU.
Therefore the use of this product should be based on local (regional, farm)
epidemiological information about susceptibility of nematodes and
recommendations on how to limit further selection for resistance to
anthelmintics.

i) Special precautions for use in animals
Divide doses greater than 10 ml between two injection sites to reduce
occasional discomfort or site reaction.
The timing of treatment for the parasitic stages of warbles should be
chosen carefully. The best time to treat against infections with
is immediately after the end of the swarming of the warbles, before the
larvae cause damage in the body of the animal (October to November). If
larvae of
this may induce posterior paralysis and recumbency. These reactions
occur mainly when animals are treated between December and March.
Avermectins may not be well tolerated in non-target species. Cases of
intolerance resulting in fatalities have been reported in dogs, especially
collies, old English sheep dogs and related breeds or crosses and also in
turtles/tortoises.
ii) Special precautions to be taken by the person administering the
veterinary medicinal product to animals
Do not smoke, drink or eat while handling the product.
Wash hands after use.
Avoid contact with skin and eyes.
Take care to avoid self-administration, the product may cause irritation
and/or pain at the site of injection. In case of accidental self-injection,
seek medical advice and show the label to the doctor.
iii) Other precautions
Ivermectin is highly toxic to aquatic invertebrates. Treated cattle should
not have direct access to ponds, streams or ditches for 14 days after
treatment to avoid adverse effects on aquatic organisms.

Revised: April 2024
AN: 01199/2023 & 01201/2023Page 4 of 7
Not known.
Protect from light.
Store in the original container.
Meat and offal : 66 days.
Milk: do not use in animals producing milk for human consumption.
Do not use in non-lactating dairy cows including pregnant heifers within 60 days
of calving.
5.

This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.

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