Vétoquinol
Aluspray cutaneous spray for cattle, horses, swine, poultry, sheep, cats and dogs 210 ml

For the protection and healing of wounds in cattle, horses, swine, poultry, sheep, cats and dogs

This drug is unauthorized in certain countries

Aluspray 4% w/w Cutaneous Spray, Powder

2 ALUSPRAY QUALITATIVE AND QUANTITATIVE COMPOSITION

Active Substance

Aluminium powder  4.0 % w/w

Excipients

For a full list of excipients see section 6.1.

3 ALUSPRAY PHARMACEUTICAL FORM

Cutaneous spray, powder. A grey, oily powder.

4 ALUSPRAY CLINICAL PARTICULARS

4.1 Target Species

Cattle, horses, swine, poultry, sheep, dogs and cats.

4.2 Indications for use, specifying the target species

For the protection and healing of wounds.

4.3 Contraindications

Do not use in case of hypersensitivity to the active substance or to any of the excipients.
Do not use in animals suffering from severe renal impairment.
Do not use to treat teat injuries in lactating animals producing milk for human consumption.

4.4 Special warnings for each target species

None.

4.5 Special precautions for use

Special precautions for use in animals
The product should be used unaltered from the original container. In case of blockage of the spray nozzle, immerse it in hot water.
Special precautions to be taken by the person administering the veterinary medicinal product to animals
This product stains: avoid contact with hands and clothes.

Wear gloves when administering the product, wash hands after use. Treat animals outdoor or in a well ventilated area.
Avoid inhalation. Do not swallow.
Pressurised container.
Flammable.

Do not spray on or near a naked flame or any incandescent material.

4.6 Adverse reactions (frequency and seriousness)

None.

4.7 Use during pregnancy, lactation or lay

Pregnancy:

Can be used during pregnancy.

Lactation:

Do not use to treat teat injuries in lactating animals producing milk for human consumption.

4.8 Interaction with other medicinal products and other forms of interaction

None.

4.9 Amounts to be administered and administration route

Shake well before use.

A superficial application onto wounds once or twice daily, to produce a fine coating of the powder. For optimal use, wounds should be cleaned, disinfected and sutured if necessary before the application of Aluspray.

4.10 Overdose (symptoms, emergency procedures, antidotes), if necessary

None.

4.11 Withdrawal Period(s)

Zero days.

Not authorised for use in lactating animals producing milk for human consumption.

5 ALUSPRAY PHARMACOLOGICAL or IMMUNOLOGICAL PROPERTIES

Pharmacotherapeutic group: Dermatologicals, antiseptics and disinfectants, aluminium agents. ATC vet code: QD08AB
Micronised aluminium has long been used for the healing of wounds. It accelerates wound healing and has an antimicrobial effect due to the elimination of micro organisms from the tissues which it covers.
Aluspray allows a fine mist of aluminium to be produced permitting complete covering of lesions. The film thus obtained affords good protection against dirt and insects.

6 ALUSPRAY PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Liquid paraffin Liquified petroleum gas Stearic acid

6.2 Incompatibilities

None known.

6.3 Shelf-life

Shelf life of the veterinary medicinal product as packaged for sale: 36 months.

6.4 Special precautions for storage

Do not store above 25oC. Protect from direct sunlight.

6.5 Nature and composition of immediate packaging

This product is packed in an aluminium 210 ml pressurised can equipped with a valve.

6.6 Special precautions for the disposal of unused veterinary medicinal products or waste materials

Do not pierce or burn even after use.
Any unused product or waste material should be disposed of in accordance with national requirements.

7 MARKETING AUTHORISATION HOLDER

Vetoquinol Ireland Limited First Floor, Segrave House 19/20 Earlsfort Terrace Dublin 2

11.90
Order within 9h 12m 18s (before 12AM)
And receive your order
on Wednesday 20 November
AIR FREIGHT

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