Imidacloprid EU Pharma 100 mg Spot-on Solution for Medium Dogs

Kraj: Wielka Brytania

Język: angielski

Źródło: VMD (Veterinary Medicines Directorate)

Kup teraz

Składnik aktywny:

Imidacloprid

Dostępny od:

EU Pharmaceuticals Ltd

Kod ATC:

QP53AX17

INN (International Nazwa):

Imidacloprid

Forma farmaceutyczna:

Spot-on solution

Typ recepty:

AVM-GSL - Authorised Veterinary Medicine – General Sales List

Grupa terapeutyczna:

Dogs

Dziedzina terapeutyczna:

Ectoparasiticide

Status autoryzacji:

Expired

Data autoryzacji:

2019-07-09

Charakterystyka produktu

                                Issued: July 2019
AN: 02294/2017
Page 1 of 6
SUMMARY OF PRODUCT CHARACTERISTICS
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Imidacloprid EU Pharma 100 mg Spot-on solution for Medium Dogs
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each 1 ml contains:
ACTIVE SUBSTANCE:
Imidacloprid
100 mg
EXCIPIENTS:
Butylhydroxytoluene (E 321)
1.0 mg
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Spot-on solution
Clear yellow to slightly brownish solution.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Dogs
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the prevention and treatment of flea infestations and for the
treatment of biting
lice _(Trichodectes canis) _on dogs from 4 kg to less than 10 kg body
weight.
Fleas on dogs are killed within one day following treatment. One
treatment prevents
further flea infestation for four weeks.
4.3
CONTRAINDICATIONS
Do not treat unweaned puppies of less than 8 weeks of age.
Do not use in case of hypersensitivity to the active substance or to
any of the
excipients.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
If signs of disease persist or appear, consult a veterinary surgeon.
Issued: July 2019
AN: 02294/2017
Page 2 of 6
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
This product is for topical use and should not be administered orally.
Care should be taken to avoid the contents of the pipette coming into
contact with the
eyes or mouth of the recipient animal.
Do not allow recently treated animals to groom each other.
Special precautions to be taken by the person administering the
veterinary medicinal
product to animals
This product can cause mucous membrane, skin and eye irritation.
Therefore, contact of the product with mouth, skin and eyes should be
avoided.
This product contains benzyl alcohol and may cause skin sensitisation
or transient
skin reactions in rare cases (for example, irritation, tingling).
People with a known hypersensitivity (allergy) to insecticides or
alcohol should avoid
contact with the product.
Do not smoke, dri
                                
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