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POM-VPS Prescription Required

Topimec 5 mg/ml Pour-on Solution

Active ingredient: Ivermectin

Form

Spot-on

Species

Cattle

Manufacturer

Chanelle Pharmaceuticals Manufacturing Ltd

VMD MA No.

08749/5182

What it's used for

For the treatment of infections with the following species of gastrointestinal roundworms, lungworms, warbles, mites and lice for beef and non-lactating da...

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

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Prescription required

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Clinical information

Topimec 5 mg/ml Pour-on Solution — SPC Details

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

For the treatment of infections with the following species of gastrointestinal
roundworms, lungworms, warbles, mites and lice for beef and non-lactating dairy
cattle:
Gastro-intestinal roundworms (adults and fourth stage larvae):
Ostertagia ostertagi)
Haemonchus placei
Trichostrongylus axei
Trichostrongylus colubriformis
Cooperia spp
Oesophagostomum radiatum
Strongyloides papillosus (adult only)
Lungworms (adult and fourth stage larvae):
Dictyocaulus viviparus

Amended pages: November 2025
AN: 01686/2025
Eye worms (adult):
Thelazia spp
Warbles (parasitic stages):
Hypoderma bovis
Hypoderma lineatum
Mites:
Chorioptes bovis (reduction of infestation)
Sarcoptes scabiei var bovis.
Sucking lice:
Linognathus vituli
Haematopinus eurysternus
Biting Lice:
Damalinia bovis
The product given at the recommended dosage of 500 micrograms/kg bodyweight,
has persistent activity against and
during the 14 days after treatment, only if the whole herd is treated simultaneously. It
also has a persistent activity against and
radiatum acquired during the first 21 days after treatment and
(lungworm) acquired during the first 28 days after treatment. It also has a persistent
activity on horn flies (Haematobia irritans) for 28 days after treatment, partial efficacy
may last for up to 35 days post application. Occasionally variable activity may be
observed against and
Trichostrongylus colubriformis.
For single topical administration.
Dosage: 1 ml per 10 kg bodyweight (based on a recommended dose of 500
micrograms/kg bodyweight).
To ensure administration of a correct dose, body weight should be determined as
accurately as possible.
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.
Administration: Pour-on use. The formulation should be applied along the mid-line of
the back in a narrow strip between the withers and tailhead. The product should be
used with appropriate dosing equipment. The interval between 2 treatments should
be at least 28 days.
Do not use in cases of known hypersensitivity to the active ingredient.
The product has been formulated for topical application specifically for cattle. It
should not be administered to other species as severe adverse reactions, including
fatalities in dogs, may occur.
Occasionally slight irritation at the application site may occur. However, usually these
irritations rapidly disappear without treatment.
Do not treat cattle when hair or hide is wet. Do not treat cattle if rain is expected, as
rain within two hours of treatment may reduce efficacy. However, the efficacy of the
product against established infections of O. ostertagi or D. viviparus is not adversely
affected if the hide is wet or if rain falls shortly after treatment.
Do not apply to areas of skin that may have mange scabs or other lesions or to areas
contaminated with mud or manure.
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.

Amended pages: November 2025
AN: 01686/2025
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 ivermectin has been reported in Cooperia spp. and in
ostertagi in cattle. Resistance has also been reported in in
cattle outside the EU. Therefore, the use of this product should be based on local
(region, farm) epidemiological information about susceptibility of this helminth species
and recommendations on how to limit further selection for resistance to anthelmintics.

Special precautions for use in animals
Ivermectins may not be well tolerated in all non-target species. Cases of intolerance
with fatal outcome are reported in dogs, especially Collies, Old English Sheepdogs
and related breeds or crosses, and also in turtles/tortoises. To avoid secondary
reactions due to the death of larvae in the oesophagus or in the spine, it
is recommended to administer the product at the end of the period of warble fly
activity and before the larvae reach their resting site. As Ivermectin is extremely
dangerous to fish and aquatic life, treated animals should not have direct access to
surface water and ditches during treatment.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
The product may be irritating to human skin and eyes and the user should be careful
not to apply it to himself or other persons. Operators should wear rubber gloves and
boots with a waterproof coat when applying the product. Protective clothing should
be washed after use. Use only in well-ventilated areas or outdoors.
HIGHLY FLAMMABLE.
Keep away from heat, spark, open flame or other source of ignition. Do not eat, drink
or smoke whilst handling the product.
As absorption through skin can occur, in the event of accidental skin contact the
affected area should be washed immediately with soap and water. If irritation
persists, seek medical advice and show the package label to the doctor.
If accidental eye exposure occurs, flush the eyes immediately with water and seek
medical attention. Wash hands after use.
For external use only.
Other precautions
The influence of extreme climatic conditions on persistent activity of the product is
unknown. 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 repeat treatments on a pasture with in a season
should only be given on the advice of the veterinarian.

Amended pages: November 2025
AN: 01686/2025
None known.
Highly Flammable – keep away from heat, sparks, open flame or other sources of
ignition. Close container when not in use. Bottles should remain upright during
storage. Protect from light. Store in tightly closed original container.

Amended pages: November 2025
AN: 01686/2025
Excipient(s):
For the full list of excipients, see section

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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