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POM-V Prescription Required Companion Animal

Advantix 600 mg + 3000 mg Spot-on Solution for Dogs (> 40 kg ≤ 60 kg)

Active ingredients: Imidacloprid, Permethrin (Cis:Trans 40:60)

Form

Spot-on

Species

Dogs

Manufacturer

Elanco GmbH

VMD MA No.

52127/5127

What it's used for

used against all the following parasite species is required at the same time. For the treatment and prevention of flea (Ctenocephalides canis, Ctenocephali...

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

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Clinical information

Advantix 600 mg + 3000 mg Spot-on Solution for Dogs (> 40 kg ≤ 60 kg) — SPC Details

Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.

used against all the following parasite species is required at the same time.
For the treatment and prevention of flea (Ctenocephalides canis, Ctenocephalides
felis) infestation.
Fleas on dogs are killed within one day following treatment. One treatment prevents
further flea infestation for four weeks. The veterinary medicinal product can be used
as part of a treatment strategy for flea allergy dermatitis (FAD).
Treatment of biting lice (Trichodectes canis).
The veterinary medicinal product has persistent acaricidal and repellent efficacy
against tick infestations (Rhipicephalus sanguineusIxodes ricinus for four weeks,
and Dermacentor reticulatus
Reduction of the risk of transmission of the vector-borne pathogen Ehrlichia canis,
thereby reducing the risk of canine ehrlichiosis by acaricidal and repellent activity on
the tick vector Rhipicephalus sanguineus.
begin from three days following application of the veterinary medicinal product and to
persist for four weeks.
Ticks already on the dog may not be killed within two days after treatment and may
remain attached and visible. Therefore the removal of ticks already on the dog at the
time of treatment is recommended, in order to prevent them from attaching and
having a blood meal.
One treatment provides repellent (anti-feeding) activity against sand flies
(Phlebotomus papatasiPhlebotomus perniciosus
against mosquitoes (Aedes aegypti for two weeks and Culex pipiens
and against stable flies (Stomoxys calcitrans) for four weeks.
Reduction of the risk of transmission infection of the vector-borne pathogen
Leishmania infantum, thereby reducing the risk of canine leishmaniosis by repellent
(anti-feeding) activity on sandflies (vector Phlebotomus papatasi
vector Phlebotomus perniciosus
veterinary medicinal product’s activity against the vector.
The recommended minimum dose is:
10 mg/kg body weight (bw) imidacloprid and 50 mg/kg body weight (bw) permethrin.
Dosing Scheme
Dogs (kg bw)Trade nameVolume
(ml)
Imidacloprid
(mg/kg body
weight)
Permethrin
(mg/kg body
weight)
> 40 kg  60
kg
Advantix 600 mg +
3000 mg
6.0 ml10 - 1550- 75
For dogs > 60 kg the appropriate combination with other sized pipettes should be
used.
Underdosing could result in ineffective use and may favour resistance development.
To ensure a correct dosage, body weight should be determined as accurately as
possible.
Ticks, fleas:
The need and frequency of re-treatment(s) should be based on local epidemiological
situation and the animal’s lifestyle.
Biting lice:
In case of biting louse infestation, a further veterinary examination 30 days after
treatment is recommended as some animals may require a second treatment.
Sand flies:
To protect a dog over the whole sand fly season, treatment should be compliantly
continued throughout.
Method of administration
Remove one pipette from the package. Hold applicator pipette in an upright position,
twist and pull cap off. Turn the cap around and place the other end of cap back on
pipette. Twist cap to break seal, then remove cap from pipette.
With the dog standing still, the entire contents of the pipette should be applied evenly
to four spots on the top of the back from the shoulder to the base of the tail. At each
spot, part the hair until the skin is visible. Place the tip of the pipette on the skin and
gently squeeze to expel a portion of the solution on the skin. Do not apply an
excessive amount of solution at any one spot that could cause some of the solution
to run off the side of the dog.
In the absence of available data the veterinary medicinal product should not be used
on puppies of less
than 7 weeks of age or 40 kg of weight.
Do not use in cases of hypersensitivity to the active substances or to any of the
excipients.
Do not use on cats. (See section 3.5).
Dogs.
Uncommon
(1 to 10 animals / 1,000 animals
treated):
Application site hair change (e.g. greasy fur),
Application site itching
Vomiting
Rare
(1 to 10 animals / 10,000
animals treated):
Application site erythema, Application site hair
loss, Application site inflammation
Diarrhoea
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Agitation
1,2,4
, Restlessness
1,2,4
, Rolling
1,2,4
,
Whining
1,2,4
Hypersalivation
1,2,4
Decreased appetite
1,2,4
, Lethargy
1,3
Neurological signs (Abnormal movement and
Twitching)
1,2,4
, Tremor
Rubbing
1,4
, Scratching
1,4
Generally self-resolving.
In dogs susceptible to permethrin.
Following inadvertent oral uptake in dog. There is no known specific antidote;
symptomatic treatment recommended.
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 the package leaflet for respective contact details.
It is recommended to apply the treatment at least three days before expected
exposure to Ehrlichia. canis. With regard to E. canis, studies have demonstrated a
reduced risk of canine ehrlichiosis in dogs exposed to Rhipicephalus sanguineus
ticks infected with E. canis from three days following application of the veterinary
medicinal product and to persist for four weeks.
Immediate protection against sandflies bites is not documented. Treated dogs for the
reduction of the risk of infection with Leishmania infantum via transmission by
sandflies Phlebotomus. perniciosus
the first 24 hours after the initial treatment application.
To reduce re-infestation from emergence of new fleas, it is recommended to treat all
dogs in a household. Other animals living in the same household should also be
treated with a suitable product. To aid further in reducing environmental challenge,
the additional use of a suitable environmental treatment against adult fleas and their
developmental stages is recommended.
The veterinary medicinal product remains effective if the animal becomes wet.
However, prolonged, intense exposure to water should be avoided. In cases of
frequent water exposure the persistent efficacy may be reduced. In these cases do
not retreat more frequently than once weekly. If a dog requires a shampoo, it should
be administered before applying the veterinary medicinal product or at least 2 weeks
after application, to optimise efficacy of the veterinary medicinal product.
The possibility that other animals in the same household can be a source of re-
infection with fleas, biting lice, ticks, mosquitoes and flies should be considered, and
these should be treated as necessary with an appropriate product.
In the absence of risk of co-infection, a narrow spectrum veterinary product should be
used. The use of this veterinary medicinal product should take into account local
information about susceptibility of the target parasites, where available.
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 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.
In Europe, resistance to pyrethroids has been reported in isolated cases of
Rhipicephalus sanguineusStomoxys calcitrans. Current knowledge suggests
that resistance in both parasites is conferred by gene mutations at the target site
while other factors like metabolic detoxification may also play a role.

Special precautions for safe use in the target species:
Care should be taken to avoid the content of the pipette coming into contact with the
eyes or mouth of the recipient dogs.
Care should be taken to administer the veterinary medicinal product correctly as
described under section 3.9. In particular oral uptake due to the licking of the
application site by treated or in contact animals should be avoided.
Do not use on cats.
This veterinary medicinal product is extremely poisonous to cats and could be fatal
due to the unique physiology of cats which is unable to metabolise certain
compounds including permethrin. To prevent cats from being accidentally exposed to
the veterinary medicinal product, keep treated dogs away from cats after treatment
until the application site is dry. It is important to ensure that cats do not groom the site
of application on a dog, which has been treated with this veterinary medicinal
product. Seek veterinary advice immediately if this occurs.
Consult your veterinary surgeon before using the veterinary medicinal product on sick
and debilitated dogs.
Ticks will be killed and fall off the host within 24 to 48 hours after infestation without
having a blood meal, as a rule. An attachment of single ticks after treatment cannot
be excluded. For this reason, a transmission of infectious diseases by ticks cannot be
completely excluded if conditions are unfavourable.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals
Avoid contact between the veterinary medicinal product and skin, eyes or mouth.
Do not eat, drink or smoke during application.
Wash hands thoroughly after use.
In case of accidental spillage onto skin, wash off immediately with soap and water.
People with known skin sensitivity may be particularly sensitive to this product.
People with known hypersensitivity to imidacloprid and permethrin should administer
the veterinary medicinal product with caution. The predominant clinical symptoms
that in extremely rare case may be shown are transient sensory irritations of the skin
like tingling, burning sensation or numbness.
If the veterinary medicinal product gets accidentally into the eyes, the eyes should be
thoroughly flushed with water.
If skin or if eye irritation persists, seek medical advice immediately and show the
package leaflet or the label to the physician.
Do not ingest. In case of accidental ingestion, seek medical advice immediately and
show the package leaflet or the label to the physician.
Treated dogs should not be handled especially by children until the application site is
dry. This may be ensured by treating the dogs e.g. in the evening. Recently treated
dogs should not be allowed to sleep together with their owner, especially children.
In order to prevent children from getting access to pipettes, keep the pipette in the
original packaging until ready for use and dispose of used pipettes immediately.
Laboratory studies in rabbits and rats with the excipient N-methylpyrrolidone have
shown evidence of foetotoxic effects. The veterinary medicinal product should not be
administered by pregnant women and women suspected of being pregnant. Personal
protective equipment consisting of gloves should be worn when handling the
veterinary medicinal product by women of childbearing age.
Special precautions for the protection of the environment:
As the veterinary medicinal product is dangerous to aquatic organisms, treated dogs
must not under any circumstances be allowed into any type of surface water for at
least 48 hours after treatment.
Other precautions:
The solvent in this veterinary medicinal product may stain certain materials including
leather, fabrics, plastics and finished surfaces. Allow the application site to dry before
permitting contact with such materials.
None known.
Do not freeze.
After opening the foil pouch store in a dry place at a temperature not above 30°C.
Not applicable

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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