Instructions for Medical bile 250 ml
Medical bile 250 ml
English product name
Bile medicine conserved
Release Form
Emulsion for Outdoor Application
Description Medical bile
Emulsion for external application from yellow-brown to dark-brown with a greenish tint or from light-green to dark-green with a brownish tint, with a characteristic smell; sediment may be present.
1.013 l
defrosted bile 900ml
* bile from cattle and pigs is obtained.
Auxiliary substances: 96% ethyl alcohol - 100 ml, solution of furacilin in alcohol 70% - 10 ml, formalin - 1 ml, flavoring - 2 ml.
100 ml - glass bottles (1) - cardboard packs.
250 ml - glass bottles (1) - cardboard packs.
100 ml - polyethylene terephthalate bottles (1) - cardboard packs.
250 ml - polyethylene terephthalate bottles (1) - cardboard packs.
ATC codes
M02AX10 Other drugs
Clinical-pharmacological groups / Group affiliation
Preparation with local irritating effect for external use
Active substance
bile of cattle and pigs, defrosted
Pharmaco-therapeutic group
Local irritant
Storage Conditions
The drug should be stored in a place inaccessible to children, protected from light at a temperature of 4° to 25°C.
Best before date
The shelf life is three years.
Pharmacological effect Medical bile
The preparation, which is obtained from the bile of cattle and pigs, has a local irritating effect.
Testimony Medical bile
- arthralgia;
- post-traumatic myalgia (without disturbing the integrity of the skin).
Use in children
The use of the preparation in children under 12 years of age is contraindicated.
With caution, you should use the drug in children over 12 years.
- Nosology (ICD codes)
- M25.5
- Joint pain
- M79.1
- Mialgia
Method of use, course and dosage Medical bile
The preparation is used externally in the form of compresses. The gauze napkin (in 4-6 layers), impregnated with the preparation, is applied to the intact areas of the skin in the lesion area, covered with waxed paper, a thin layer of cotton wool and fixed with a light bandage.
The compress with the drug is maintained for a day. When drying, the gauze napkin is moistened with room-temperature water and fixed again with a bandage. After a day, the compress is changed using a new gauze napkin.
The course of treatment is six to ten days.
If no improvement occurs after treatment or the symptoms become worse or new symptoms appear, the patient should consult a doctor.
The drug should be used according to the indications, the method of use and in the doses specified in the instructions.