Bravecto CombiUNO Chewable Tablets for Dogs (> 5.0 – 10.0 kg)
Active ingredients: Fluralaner, Milbemycin Oxime (A3 and A4)
Form
Chewable
Species
Manufacturer
Intervet International B.V.
VMD MA No.
EU/2/25/350/007-009
What it's used for
For the treatment of tick and flea infestations in dogs. This veterinary medicinal product is a systemic insecticide and acaricide that provides: -Ctenocep...
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Paying less for Fluralaner + Milbemycin Oxim...
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1
Ask your vet for a written prescription
They must provide one on request. Under the CMA Order the fee is capped at £21 from 2027.
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2
Fill it at a registered online retailer
The CMA found online pharmacies 50–60% cheaper than practice dispensing on common medicines — typically £200–£300 a year.
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Prescription required
Your vet must provide a written prescription on request. You can then purchase from any licensed online retailer.
Bravecto CombiUNO Chewable Tablets for Dogs (> 5.0 – 10.0 kg) — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
This veterinary medicinal product is a systemic insecticide and acaricide that
provides:
-Ctenocephalides felis
-
Dermacentor reticulatus and D. variabilis,
-Rhipicephalus
sanguineus,
-Ixodes
hexagonus.
Fleas and ticks must attach to the host and commence feeding in order to be
exposed to the active substance.
The veterinary medicinal product can be used as part of a treatment strategy for the
control of flea allergy dermatitis (FAD).
For the treatment of demodicosis caused by Demodex canis.
For the treatment of sarcoptic mange (Sarcoptes scabiei var. canis) infestation.
Revised: August 2025
AN: 00732/2025
For reduction of the risk of infection with Babesia canis canis via transmission by
Dermacentor reticulatus for up to 12 weeks. The effect is indirect due to the
veterinary medicinal product’s activity against the vector.
For reduction of the risk of infection with Dipylidium caninum via transmission by
Ctenocephalides felis for up to 12 weeks. The effect is indirect due to the veterinary
medicinal product’s activity against the vector.
excipients.
Common
(1 to 10 animals / 100 animals treated):
Gastrointestinal effects (such as
Anorexia, Hypersalivation, Diarrhoea,
Emesis)
#
.
Very rare
(<1 animal / 10,000 animals treated,
including isolated reports):
Lethargy;
Pruritus;
Muscle tremor, Ataxia, Convulsion.
# mild and transient
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 also the last section of the
package leaflet for respective contact details.
therefore the risk of the transmission of parasite borne diseases (including Babesia
canis canis and D. caninum) cannot be completely excluded.
Unnecessary use of antiparasitics or use deviating from the instructions given in the
SPC may increase the resistance selection pressure and lead to reduced efficacy.
The decision to use the veterinary medicinal product should be based on
confirmation of the parasitic species and burden, or of the risk of infestation based on
its epidemiological features, for each individual animal.
The possibility that other animals in the same household can be a source of re-
infection with parasites should be considered, and these should be treated as
necessary with an appropriate veterinary medicinal product.
Special precautions for safe use in the target species:
Use with caution in dogs with pre-existing epilepsy.
In the absence of available data, the veterinary medicinal product should not be used
on puppies less than 8 weeks old and /or dogs weighing less than 2 kg.
The veterinary medicinal product should not be administered at intervals shorter than
8 weeks as the safety for shorter intervals has not been tested.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Keep the veterinary medicinal product in the original packaging until use, in order to
prevent children from getting direct access to the veterinary medicinal product.
Hypersensitivity reactions in humans have been reported.
Do not eat, drink or smoke while handling the veterinary medicinal product.
Wash hands thoroughly with soap and water immediately after use of the veterinary
medicinal product.
Special precautions for the protection of the environment:
Not applicable.
Other precautions:
Not applicable.
Revised: August 2025
AN: 00732/2025
bound active substances such as non-steroidal anti-inflammatory drugs (NSAIDs)
and the coumarin derivative warfarin. Incubation of fluralaner in the presence of
carprofen or warfarin in dog plasma at maximum expected plasma concentrations did
not reduce the protein binding of fluralaner, carprofen or warfarin.
During clinical field testing, no interactions between the veterinary medicinal product
and routinely used veterinary medicinal products were observed.
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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Related Conditions
Other Products Containing Fluralaner
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Bravecto
POM-VBravecto 1 000 mg Chewable Tablets for Large Dogs (>20 – 40 kg)
POM-VIntervet International B.V.
Bravecto 1 000 mg Chewable Tablets for Large Dogs (>20 – 40 kg)
POM-VMSD Animal Health UK Limited
Bravecto 1 000 mg spot-on solution for large dogs (>20 – 40 kg)
POM-VIntervet International B.V.
Bravecto 1 000 mg Spot-on Solution for Large Dogs (>20 – 40 kg)
POM-VMSD Animal Health UK Limited
Bravecto 1 400 mg Chewable Tablets for Very Large Dogs (>40 – 56 kg)
POM-VIntervet International B.V.
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