Olazol spray 80g vials

Description

Composition
Active substance:
Sea buckthorn oil 7.20 g
Chloramphenicol 2.16g
Benzocaine (benzocaine) 2.16 g
Boric acid 0.36 g
Excipients:
Trolamine 2.16 g
Anhydrous Lanolin 0.36 g
Stearic acid 2.88 g
Glycerol (glycerin) 7,20 g
Purified water 47.52 g
A mixture of 6.00 g of Freon or 8.00 g
Description:
The drug at the outlet of the cylinder forms a foam yellow or yellow orange color with a slight tinge.
Product form:
An aerosol for external use.
80 g of aluminum aerosol cans fitted with a continuous valve, spray nozzle and the protective cap.
Each cylinder is placed in a pile of cardboard. The text of the instructions for use printed on the package.
Contraindications
Increased sensitivity to the drug. Pregnancy, breastfeeding, neonatal period.
Carefully:
Early childhood.
Indications
Infected wounds (including wound vyalozazhivayuschie), trophic ulcers, burns, free dermepenthesis, microbial eczema, itchy dermatitis.
Interaction with other drugs
During treatment, you can use systemic antibiotic therapy.
The possibility and need for other external drugs is determined individually by the attending physician, depending upon the nature of the inflammation and the regeneration of damaged tissue stages.
When applied simultaneously with erythromycin, clindamycin, lincomycin possibly weakening the mutual action due to the fact that chloramphenicol can displace these drugs from a bound state or inhibit their binding to the 50S subunit of bacterial ribosomes. Chloramphenicol reduces the antibacterial effect of penicillins, cephalosporins.
If you apply the above or other medications (including over the counter) before using Olazol® drug, consult your physician.
Overdose
Data on overdose lacking
pharmachologic effect
Pharmacological group:
an antimicrobial agent combined.
Pharmacological properties:
Healing wounds. Anesthetic and provides an antibacterial effect, reduces exudation promotes tissue regeneration and accelerates epithelialization of wounds.
Pregnancy and breast-feeding
Application of pregnancy and lactation is contraindicated.
Conditions of supply of pharmacies
Without a prescription.
side effects
Allergic reactions. If you have marked side effects indicated in the instructions or they are compounded, or if you notice any other side effects not mentioned in the instructions, tell your doctor.
special instructions
Avoid contact with eyes.
Effects on ability to drive vehicles, mechanisms:
It does not affect the ability to drive vehicles or work with other potentially dangerous machinery.
Storage conditions
The temperature is not above 15 degrees, away from sources of ignition, heating appliances and direct sunlight.
Keep out of the reach of children
Dosing and Administration
Outwardly. Wound surface as possible was purified by pus, necrotic tissue and covered with a uniform layer of foam on a daily basis or every other day, and for the treatment of open wounds and burns – 1-4 times a day, depending on the nature of inflammation and regeneration of damaged tissue stages. The course of treatment is determined individually by the attending physician.
To obtain a uniform layer of foam necessary to shake the cylinder (10-15 times). The foam is applied to cover the entire wound surface with a distance of 1-5 cm.
If after treatment there is no improvement or symptoms are aggravated, or there are new symptoms, you should consult with your doctor.
Use according to the drug only indications that the application and in those doses which are specified in the instruction.
Information
Appearance may differ from that depicted in the picture. There are contraindications. You need to read the manual or consult with a specialist