Alumispray aerosol 170ml

DESCRIPTION

Alumispreum (Alumispreum) - suspension for external use for treating wounds in animals. In appearance, the drug is an opaque gray suspension.

COMPOSITION

Aluminum spray contains in 100 ml aluminum powder (aluminum oxide) - 9.6 g as an active ingredient and auxiliary substances - pine rosin, BF-6 glue and ethyl alcohol.

PHARMACOLOGICAL PROPERTIES

Pharmacotherapeutic group of the drug: drugs for the treatment of skin diseases.

Aluminum powder (aluminum oxide) in the composition of Alumisprey has an adsorbing and drying effect, thus accelerating the healing of damaged tissue.

According to the degree of impact on the body, according to GOST 12.1.007-76, Alumisprey belongs to low-hazard substances (hazard class 4), in the recommended doses and concentrations it does not have a skin-irritating and resorptive-toxic effect.

DOSAGE AND APPLICATION

Aluminum spray is used to treat wounds in animals.

The drug is applied topically topically. Before applying the drug, it is necessary to sanitize the wound surface, in case of severe bleeding, stop it.

Shake the aerosol can (propellant-free bottle) thoroughly and apply the drug by holding the can (bottle) vertically at a distance of 15-20 cm from the wound. The amount of drug used depends on the size and condition of the wound surface. Finish the application of the preparation when its uniform layer is formed and the treated area acquires a characteristic gray color. Apply the drug 1-2 times a day for 5-10 days.

SPECIAL INSTRUCTIONS

Overdose symptoms were not revealed in animals.

The peculiarities of the action of the drug during the first use or when it is canceled have not been established.

The use of Alumisprey does not affect the course of pregnancy and the development of offspring in animals. Do not use the drug for treating udder nipple wounds in animals during lactation and feeding young animals during the neonatal period.

In case of an accidental increase in the interval between two treatments, the preparation should be applied as soon as possible and further treatments should be continued at the recommended interval.

Alumisprey should not be administered concurrently with other topical medications.

Products of animal origin obtained from animals after the use of Alumisprey can be used without restriction. In the event of a forced slaughter of an animal, the carcass areas treated with Alumisprey are cleaned and disposed of.

CONTRAINDICATIONS

A contraindication for the use of the drug is the individual hypersensitivity of the animal to the components of the drug. Do not use the drug for treating udder nipple wounds in animals during lactation and feeding young animals during the neonatal period.

SIDE EFFECTS

When using Alumisprey in accordance with this instruction, side effects and complications are usually not observed.

SHELF LIFE AND STORAGE

The shelf life of the drug, subject to storage conditions, is 4 years from the date of production. It is forbidden to use Alumisprey after the expiration date.

Store the medicinal product in the manufacturer's closed packaging away from heating devices, separately from food and feed, in a dry place protected from direct sunlight at a temperature of 50 C to 250 C.

PACKAGING

Alumispray is produced in 170 ml packs in aerosol cans with spray heads and protective caps. Each consumer package is supplied with instructions for use.

Specifications

Bonus points

0

KolVUP

15

Manufacturer

BioChimPharm

Temperature regime

from +5 to +25

Teaser

for treating wounds in animals