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POM-VPS Prescription Required

Animec Super 10 mg/ml / 100 mg/ml Solution for Injection for Cattle

Active ingredients: Clorsulon, Ivermectin

Form

Injection

Species

Cattle

Manufacturer

Chanelle Pharmaceuticals Manufacturing Ltd

VMD MA No.

08749/3024

What it's used for

For the treatment of mixed infestation of adult liver fluke and gastro-intestinal roundworms, lungworms, eye worms, and/or mites and lice of beef and non-l...

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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    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

Animec Super 10 mg/ml / 100 mg/ml Solution for Injection for Cattle — SPC Details

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

For the treatment of mixed infestation of adult liver fluke and gastro-intestinal roundworms,
lungworms, eye worms, and/or mites and lice of beef and non-lactating dairy cattle.
Gastrointestinal Roundworms (adult and fourth-stage larvae):
Ostertagia ostertagi (including inhibited larval stages)
O. lyrata
Haemonchus placei
Trichostrongylus axei
T. colubriformis
Cooperia oncophora
C. punctata
C. pectinata
Bunostomum phlebotomum
Oesophagostomum radiatum
Strongyloides papillosus (adult)
Nematodirus helvetianus (adult)
Nematodirus spathiger

Revised: September 2025
AN: 01687/2025
Trichuris spp. (adult)
Lungworm (adult and fourth-stage larvae):
Dictyocaulus viviparus
LIVER FLUKE (ADULT):
Fasciola hepatica
EYE WORMS (ADULT):
Thelazia spp.
Warbles (parasitic stages):
Hypoderma bovis
H. lineatum
MANGE MITES:
Psoroptes bovis
Sarcoptes scabiei var. bovis
Sucking Lice:
Linognathus vituli
Haematopinus eurysternus
Solenopotes capillatus
The product may also be used as an aid in the treatment of biting lice (Damalinia bovis
and the mange mite Chorioptes bovis, but complete elimination may not occur.
Persistent Activity
The product given at the recommended dosage of 1 ml/50 kg bodyweight controls re-
infection with , , acquired up
to 14 days after treatment, and acquired
up to 21 days after treatment and acquired up to 28 days after
treatment.
Dosage and duration of treatment
For subcutaneous use.
A single dose of 1ml of the product per 50kg bodyweight, i.e. 200µg ivermectin and 2mg
clorsulon per kg bodyweight.
Method of administration
The product should be administered only by subcutaneous injection under the loose skin in
front of or behind the shoulder.
Divide doses greater than 10ml between two injection sites. A sterile 17 gauge (15-20
mm) needle is recommended.
Different injection sites should be used for other parenteral products administered
concurrently. When using the 500 ml pack size use only automatic syringe equipment. For
the 50 ml pack size, use of a multidose syringe is recommended.
The timing of treatment should be based on epidemiological factors and should be
customised for each individual farm. A dosing program should be established by a
qualified professional person.
To ensure a correct dosage, 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, to avoid under- or over-
dosing, they should be grouped according to their bodyweight and dosed accordingly.
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.
Do not use this product intravenously or intramuscularly. This product is a low volume
product authorised for use in cattle. It must not be used in other species as severe adverse
reactions, including fatalities in dogs, may occur, especially Collies, Old English
Sheepdogs and related breeds or crosses. Do not use in animals with a known sensitivity
to the active ingredient or to any of the excipients.
Transient discomfort has been observed in some cattle following subcutaneous
administration. A low incidence of soft tissue swelling at the site of injection has been
observed. These reactions disappeared without treatment.
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: September 2025
AN: 01687/2025
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
Ostertagia ostertagi and spp. 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
This product does not contain any antimicrobial preservative. Swab septum before
removing each dose. To avoid secondary reactions due to the death of Hypoderma larvae
in the oesophagus or the spine, it is recommended to administer the product at the end of
the period of fly activity and before the larvae reach their resting sites: seek professional
advice on the correct timing of treatment.
ii) Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Do not eat, drink or smoke whilst handling the product.
Wash hands after use.
Direct contact with the skin should be avoided.
Wear gloves and glasses when handling the veterinary medicinal product.
Take care to avoid self-injection: the product may cause local 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
The product is very toxic to aquatic organisms and dung insects. Treated cattle should not
have direct access to ponds, streams or ditches for 14 days after treatment. Long term
effects on dung insects caused by continuous or repeated use cannot be excluded.
Therefore repeated treatment of animals on a pasture with an ivermectin-containing
product within a season should only be given in the absence of alternative treatments or
approaches to maintain animal/flock health, as advised by a veterinarian.
None known.
Protect from light.
Keep the container in the outer carton in order to protect from light.
None known.
4.9 Amounts to be administered and administration route
Dosage and duration of treatment
For subcutaneous use.
A single dose of 1ml of the product per 50kg bodyweight, i.e. 200µg ivermectin and 2mg
clorsulon per kg bodyweight.
Method of administration
The product should be administered only by subcutaneous injection under the loose skin in
front of or behind the shoulder.
Divide doses greater than 10ml between two injection sites. A sterile 17 gauge (15-20
mm) needle is recommended.
Different injection sites should be used for other parenteral products administered
concurrently. When using the 500 ml pack size use only automatic syringe equipment. For
the 50 ml pack size, use of a multidose syringe is recommended.
The timing of treatment should be based on epidemiological factors and should be
customised for each individual farm. A dosing program should be established by a
qualified professional person.
To ensure a correct dosage, 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, to avoid under- or over-
dosing, they should be grouped according to their bodyweight and dosed accordingly.
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.
4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary
A dose of 25 ml per 50kg bodyweight (25 times the recommended dose level) may result
in injection site lesions, including tissue necrosis, oedema, fibrosis and inflammation.
No other drug-related reactions have been observed.
4.11 Withdrawal period(s)
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.

Revised: September 2025
AN: 01687/2025
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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