Bayer Heathcare Drontal Puppy Suspension - 50ml

Drontal Puppy Suspension - 50ml

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Drontal Oral Puppy Suspension - 50ml

For the treatment and control of roundworms (ascarids), in particular toxocara canis, of puppies and young dogs up to one year of age.

Legal Category: NFA-VPS


A pale red suspension for oral administration. Each ml of suspension contains 5.0 mg pyrantel (as pyrantel embonate 14.4 mg) and 15 mg febantel. The product also contains 2.05 mg sodium benzoate (E211), 2.05 mg sodium propionate (E281) and 0.25 mg ponceau 4R (E124).

To ensure that you read the most up to date product information link to

Link to Veterinary Medicines Suspected Adverse Reaction Scheme.


For the treatment of roundworm infections in puppies and young dogs up to one year of age caused by:

Ascarids         Toxocara canis, Toxascaris leonina

Hookworm      Ancylostoma caninum, Uncinaria stenocephala

Whipworm      Trichuris vulpis


The dose is 1 ml suspension/kg body weight (equivalent to 14.4 mg/kg pyrantel embonate and 15 mg/kg febantel).

Administration is by the oral route. The product may be given directly to the animal or mixed with the feed. No special dietary measures are necessary.

Mix the product by inversion of the container before withdrawing the required dose.

Through intrauterine and transmammary infection, ascarid infestation may occur in dogs at a very early age. For some animals, especially in case of severe infections, elimination of ascarids may be incomplete, and a potential risk of infections to humans can not be excluded. Where epidemiologically appropriate, it is recommended that treatment should be started at 2 weeks of age and should be performed repeatedly at suitable intervals (for example every two weeks) until weaning. Otherwise treatment should be based upon confirmed infection, for example the results of faecal examinations.

Use During Pregnancy and Lactation

This product is contra-indicated for pregnant and lactating bitches.


Contra-indications, warnings, etc

Do not use simultaneously with compounds containing piperazine.

Parasite resistance to any particular class of anthelmintic may develop following frequent repeated use of an anthelmintic of that class.

The safety of the product has not been assessed in puppies younger than 2 weeks and weighing less than 0.6 kg.

In very rare cases mild transient digestive tract signs (e.g., vomiting, diarrhoea) may occur.

The anthelmintic effects of both pyrantel (spastic paralysis) and piperazine (neuromuscular paralysis) may be antagonised when the two drugs are used together.

Doses of up to 5 times the therapeutic level of the product have been administered to puppies and young dogs without clinical signs of intolerance arising. At 10 times the recommended dose the first sign of intolerance – vomiting – was evident.

User safety

Wash hands after use.

Avoid direct contact with the skin and eyes.

In case of accidental spillage wash the affected area immediately with clean running water.

Environmental safety

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.


This unopened veterinary medicinal product does not require any special storage conditions.

After opening, store the product at a temperature not exceeding 25 ºC.

Do not use after expiry date.

Shelf-life of the veterinary medicinal product as packaged for sale: 5 years.

Shelf-life after first opening the immediate packaging: 12 weeks.


Legal category: NFA-VPS

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