Bravecto Plus 500 mg / 25 mg Spot-on Solution for Large Cats (>6.25 – 12.5 kg)
Active ingredients: Fluralaner, Moxidectin
Form
Spot-on
Species
Manufacturer
MSD Animal Health UK Limited
VMD MA No.
01708/5029
What it's used for
For cats with, or at risk from, mixed parasitic infestations by ticks or fleas and ear mites, gastrointestinal nematodes, heartworm or lungworm. The veteri...
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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 Plus 500 mg / 25 mg Spot-on Solution for Large Cats (>6.25 – 12.5 kg) — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 18 Mar 2026.
gastrointestinal nematodes, heartworm or lungworm. The veterinary medicinal product
is only indicated when use against ticks or fleas and one or more of the other target
parasites is indicated at the same time.
For the treatment of tick and flea infestations in cats providing immediate and persistent
flea (Ctenocephalides felis) and tick (Ixodes ricinus)
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 flea
allergy dermatitis (FAD).
For the treatment of infestations with ear mites (Otodectes cynotis).
Revised: September 2023
AN: 01530/2022
For the treatment of infections with intestinal roundworm (4
th
stage larvae, immature
adults and adults of Toxocara cati) and hookworm (4
th
stage larvae, immature adults
and adults of ).
When administered repeatedly at a 12-week interval, the veterinary medicinal product
continuously prevents heartworm disease caused by (see details in
section 4.9).
Prevention of aelurostrongylosis (by preventing the establishment of adult
Aelurostrongylus abstrusus responsible for clinical disease).
excipients.
Common
(1 to 10 animals / 100 animals
treated):
Skin reactions at the application site (application
site alopecia, flaking skin, application site
reddening and application site pruritus)
#
.
Uncommon
(1 to 10 animals / 1,000
animals treated):
Dyspnoea (after licking the application site),
Tachypnoea;
Hypersalivation, Emesis, Haematemesis,
Diarrhoea;
Lethargy, Pyrexia;
Mydriasis.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Anorexia;
Neurological disorders (e.g. tremor, ataxia).
#
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 the national competent authority via the
national reporting system. See also “Contact details” of the package leaflet.
Revised: September 2023
AN: 01530/2022
therefore, the risk of the transmission of parasite borne diseases cannot be excluded.
Cats in areas endemic for heartworm (or those which have travelled to endemic
areas) may be infected with adult heartworms. No therapeutic effect against adult
Dirofilaria immitis has been established. It is therefore recommended, in accordance
with good veterinary practice, that animals of 6 months of age or older and living in
areas where a vector exists, should be tested for existing adult heartworm infections
before application of the veterinary medicinal product for the prevention of heartworm
disease.
For the prevention of heartworm disease in cats that are only temporarily in endemic
areas, the veterinary medicinal product should be applied before the first expected
exposure to mosquitoes and should be continued at 12-week intervals until return to
a non-endemic area. The period between treatment and return from the endemic
areas should not exceed 60 days.
For the treatment of infections with ear mites (Otodectes cynotis) or the
gastrointestinal nematodes T. cati and A. tubaeforme
frequency of, re-treatment as well as the choice of the treatment (monosubstance or
combination product) should be evaluated by the prescribing veterinarian.
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.
Parasite resistance to any particular class of anthelmintic may develop following
frequent, repeated use of an anthelmintic of that class under specific circumstances.
Parasite control is recommended throughout the period of potential infestation risk.
The possibility that other animals in the same household can be a source of re-
infection with fleas, ear mites or gastrointestinal nematodes should be considered,
Revised: September 2023
AN: 01530/2022
and these should be treated as necessary with an appropriate veterinary medicinal
product.
Avoid frequent swimming or shampooing the animal because the maintenance of
effectiveness of the product in these cases has not been tested.
No therapeutic effect against adult A. abstrusus has been established. For the
treatment of pre-existing infections with adult . abstrusus, administration of a
product authorised for treatment of adult A. abstrusus is required.
Special precautions for use in animals
Care should be taken to avoid contact with the eyes of the animal.
Do not use directly on skin lesions.
In the absence of available data, treatment of kittens less than 9 weeks of age and
cats less than 1.2 kg bodyweight is not recommended.
Treatment of male breeding animals is not recommended.
This veterinary medicinal product is for topical use and should not be administered
orally.
Oral uptake of the veterinary medicinal product at the maximum recommended dose
of 93 mg fluralaner + 4.65 mg moxidectin/kg body weight induced some self-limiting
salivation or single incidences of vomiting immediately after administration.
It is important to apply the dose as indicated to prevent the animal from licking and
ingesting the veterinary medicinal product (see sections
glycoprotein. Therefore, during treatment with the veterinary medicinal product, other
products that can inhibit p-glycoprotein (e.g., cyclosporine, ketoconazole, spinosad,
verapamil) should only be used concomitantly according to the benefit-risk
assessment of the responsible veterinarian.
conditions. The pipettes should be kept in the sachets to prevent solvent loss or
moisture uptake. The sachets should only be opened immediateley prior to use.
Revised: September 2023
AN: 01530/2022
>
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.
Bravecto Plus 500 mg / 25 mg Spot-on Solution for Large Cats (>6.25 – 12.5 kg) Prices by Online retailer
Bravecto Plus 500 mg / 25 mg Spot-on Solution for Large Cats (>6.25 – 12.5 kg) is a prescription-only veterinary medicine (POM-V). Prices are listed for information, with every retailer shown on equal terms. To buy it online you need a written prescription from your vet, which the retailer will ask for at checkout. Under the CMA Order your vet must provide one on request, with the fee capped at £21 from 2027. Your prescription rights →
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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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