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Ivomec Super Injection for Cattle (Ivermectin and Clorsulon)

Active ingredients: Clorsulon, Ivermectin

Form

Injection

Species

Cattle

Manufacturer

Boehringer Ingelheim Vetmedica GmbH

VMD MA No.

61700/3031

What it's used for

Gastro-intestinal roundworms (adult and fourth-stage larvae): Ostertagia ostertagi O. lyrata AN: 02205/2023 & 01184/2023 Haemonchus placei Trichostrongylus...

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

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Paying less for Clorsulon + Ivermectin

  1. 1

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    They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.

  2. 2

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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

Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.

Clinical information

Ivomec Super Injection for Cattle (Ivermectin and Clorsulon) — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

Gastro-intestinal roundworms (adult and fourth-stage larvae):
Ostertagia ostertagi
O. lyrata
AN: 02205/2023 & 01184/2023
Haemonchus placei
Trichostrongylus axei
Trichostrongylus colubriformis
Cooperia oncophora
Cooperia punctata
Cooperia pectinata
Bunostomum phlebotomum
Oesophagostomum radiatum
Strongyloides papillosus (adult)
Nematodirus helvetianus (adult)
Nematodirus spathiger
Lungworms (adult and fourth-stage larvae):
Dictyocaulus viviparous
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 ,
but complete elimination may not occur.
Do not use in cattle producing milk for human consumption.
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 cases of hypersensitivity to the active substances or to any of the excipients.
Cattle
AN: 02205/2023 & 01184/2023
Undetermined frequency
(cannot be estimated from the
available data)
Discomfort
Injection site swelling
, Injection site
pain
2,3
Hypersensitivity reaction
1
Transitory.
Soft-tissue reactions, disappeared without treatment.
Slight.
Symptomatic treatment should be applied.
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or its local representative or the national
competent authority via the national reporting system. See the package leaflet for
respective contact details.
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:
- Too frequent and repeated use of anthelmintics from the same class, over an extended
period of time.
- Underdosing, which may be due to underestimation of body weight, misadministration of
the product, or lack of calibration of the dosing device (if any).
AN: 02205/2023 & 01184/2023
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.

Special precautions for safe use in the target species:
Divide doses greater than 10 ml between two injection sites to reduce occasional
discomfort or site reaction.
Frequent and repeated use may lead to the development of resistance.
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 are killed during migration through
the spine, this may induce posterior paralysis and recumbency. These reactions occur
mainly when animals are treated between December and March.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
In case of accidental self-injection, seek medical advice immediately and show the
package leaflet or the label to the physician.
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.
Special precautions for the protection of the environment:
Not applicable.
Other precautions:
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.
Store in the original container.
Protect from light.
Meat and offal: 66 days.
Milk: Do not use in cattle producing milk for human consumption.
Do not use in non-lactating dairy cows including pregnant heifers within 60
days of calving.
4.

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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