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Doramax 5 mg/ml Pour-on Solution for Cattle

Active ingredient: Doramectin

Form

Spot-on

Species

Cattle

Manufacturer

C&H Generics Ltd

VMD MA No.

40162/4038

What it's used for

For treatment of infestations of gastrointestinal roundworms, lungworms, eyeworms, warbles, sucking and biting lice, mange mites and hornfly in cattle. Gas...

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

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  1. 1

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  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

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Clinical information

Doramax 5 mg/ml Pour-on Solution for Cattle — SPC Details

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

For treatment of infestations of gastrointestinal roundworms, lungworms, eyeworms,
warbles, sucking and biting lice, mange mites and hornfly in cattle.
Gastrointestinal roundworms (adults and fourth stage larvae)
Ostertagia ostertagi (inc. inhibited larvae)
O. lyrata
Haemonchus placei
Trichostrongylus axei
T. colubriformis
Cooperia oncophora
C. punctata
C. surnabada
(syn. mcmasteri)
Bunostomum phlebotomum1
Oesophagostomum radiatum
Trichuris
1
adults

Issued November 2020
AN: 01572/2018
Lungworms (adults and fourth stage larvae)
Dictyocaulus viviparus
Eyeworms (adults)
Thelazia
Warbles (parasitic stages)
Hypoderma bovis, H. lineatum
Biting lice
Damalinia (Bovicola) bovis
Sucking lice
Haematopinus eurystemus,
Linognathus vituli,
Solenopotes capillatus
Mange mites
Psoroptes bovis,
Sarcoptes scabiei,
Chorioptes bovis
Horn fly
Haematobia irritans
Duration of activity
Following product administration, efficacy against re-infection with the following
parasites persists for the period indicated:
SpeciesDaysOstertagia ostertagi35Cooperia oncophora28Dictyocaulus viviparus42Linognathis vituli49Oesophagostomum radiatum21Damalinia (Bovicola) bovis42Trichostrongylus axei28Solenopotes capillatus35
The product also controls horn flies () for at least 42 days after
treatment.
A single treatment of 1 ml (5 mg doramectin) per 10 kg bodyweight, equivalent to 500
µg/kg bodyweight, applied topically along the mid-line of the back in a narrow strip
between the withers and tail head.
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- and over-
dosing.

Issued November 2020
AN: 01572/2018
Dosage table
Body-
weight (kg)
Dose
Volume
(ml)
Doses per 1
Litre Pack
Doses per
2.5 Litre
Pack
Doses per 3
Litre Pack
Doses per 5
Litre Pack
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.
Do not use in cases of hypersensitivity to the active substance or any of the excipients.
See section 4.5.i.

Issued November 2020
AN: 01572/2018
In rare cases small skin lesions may occur at the administration site.
The frequency of adverse reactions is defined using the following convention:
- very common (more than 1 in 10 animals treated displaying adverse reaction(s))
- common (more than 1 but less than 10 animals in 100 animals treated)
- uncommon (more than 1 but less than 10 animals in 1,000 animals treated)
- rare (more than 1 but less than 10 animals in 10,000 animals treated)
- very rare (less than 1 animal in 10,000 animals treated, including isolated reports).
For external use only.
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.
- under dosing, which may be due to underestimation of bodyweight,
misadministration of the product, or lack of calibration of a dosing device (if any).
Resistance to doramectin and other avermectins has been reported in gastro-
intestinal nematodes, especially Cooperia oncophera and Ostertagia ostertagi
cattle. Therefore, the use of this product should be based on local (regional, farm)
epidemiological information about susceptibility of the target nematodes and
recommendations on how to limit further selection for resistance to anthelmintics.
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 a different pharmacological class and having a different mode of action
should be used.
Do not apply to areas of skin that are contaminated with mud or manure.
Therapeutic efficacy for internal and external parasites is not affected by heavy rainfall
(2 cm in 1 hour) either before (20 minutes) or after (20 and 40 minutes) treatment. The
influence of extreme weather conditions on efficacy is unknown.

Special precautions for use in animals
Avermectins 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/tortoise. Care should be taken to avoid
ingestion of spilled product or access to containers by these other species.
To avoid secondary reactions due to death of Hypoderma
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 sites. Consult your veterinary
surgeon on the correct timing of treatment.
Disease associated with warble fly is notifiable in some regions.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
People with known hypersensitivity to the active substance should avoid contact with
the product. Do not smoke or eat while handling the product. Wash hands after use.
The product may be irritating to human skin and eyes and users should be careful not
to apply it to themselves or to other persons. Operators should wear rubber gloves
and boots with a waterproof coat when applying the product. Protective clothing should
be washed after use. If accidental skin contact occurs, wash the affected area
immediately with soap and water. If irritation persists, seek medical attention. If

Issued November 2020
AN: 01572/2018
accidental eye exposure occurs, flush the eyes immediately with clean water and get
medical attention. Avoid accidental inhalation of this product, as this may cause
drowsiness and dizziness. Use only in well ventilated areas or outdoors.
Highly Flammable - Keep away from heat, sparks, open flame or other sources of
ignition.
Other precautions
Doramectin is very toxic to dung fauna and aquatic organisms and may accumulate in
sediments.
The risk to aquatic ecosystems and dung fauna can be reduced by avoiding too
frequent and repeated use of doramectin (and products of the same anthelmintic class)
in cattle.
The risk to aquatic ecosystems will be reduced by keeping treated cattle away from
water bodies for five weeks after treatment.
None known.
Do not refrigerate
Protect from light
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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