Chondartron is a gel for external use for the treatment of cattle, horses and dogs with diseases of the musculoskeletal system.
As active substances, Chondartron-gel contains the following components based on aqueous solutions of ethyl alcohol (in 1000 ml): Rhododendron (Rhododendron) - 3.0 ml; Rhus toxicodendron (Sumac poisonous) - 0.6 ml; Ledum (Marsh rosemary) - 30 ml; Symphytum (Comfrey pharmacy) - 0.6 ml; Causticum (Caustic soda) - 2 Г— 10-7 g / l; Calcium fluoricum (Calcium fluoride) - 1x10-7 g / l; Apis (bee venom) - 0.02 ml; Lithium carbonicum (lithium carbonate) - 1 Г— 10-5 g / l; Sulfur (Sulfur) - 8 Г— 10-6 g / l; Comarum palustre (Marsh cinquefoil) - 30 ml, as well as as auxiliary components: rectified ethyl alcohol - 94 ml, glycerin - 22 ml, carbopol - 7.0 g, 10% ammonia solution - 10 ml, water for injection.
Hondartron gel is a complex homeopathic medicine.
Has anti-inflammatory, analgesic, chondroprotective effect in diseases of the musculoskeletal system, including rheumatoid origin.
The homeopathic components that make up Hondartron-gel selectively affect fibrous tissues (tendons, ligaments, fascia), reducing congestion in them, relieve swelling, help to relieve pain, restore metabolism in the affected joint, improve its nutrition and blood supply, prevent destruction cartilage and joint deformation.
In terms of the degree of impact on the body, the drug belongs to low-hazard substances (hazard class 4 according to GOST 12.1.007-76), does not have a local irritant and sensitizing effect.
Chondartron - gel is prescribed for therapeutic purposes in cattle, horses and dogs for diseases of the musculoskeletal system: arthritis, arthrosis, bursitis, synovitis.
DOSAGE AND APPLICATION
Chondartron-gel is applied to damaged or painful areas after their preliminary sanitization with a thin layer twice a day (morning and evening). The procedure is repeated until recovery. Chondartron Gel should not be applied to an open wound.
Overdose symptoms in animals have not been established.
The peculiarities of the action of the drug during its first use and cancellation have not been established.
Avoid missed use of the drug. If you miss one use of the drug, you must apply it as soon as possible. Further, the interval until the next use of the drug does not change.
The use of Chondartron-gel does not exclude the use of other drugs for etiotropic, pathogenetic and symptomatic therapy.
Products of animal origin during and after the application of Chondartron-gel can be used without restrictions.
A contraindication for the use of the drug is an individual intolerance to the components of the drug.
When using Chondartron-gel in accordance with this instruction, side effects and complications, as a rule, are not observed.
SHELF LIFE AND STORAGE
Store Chondartron-gel in the manufacturer's closed packaging in a dry, dark place, separately from food and feed at a temperature from 0 В° C to 25 В° C. Chondartron Gel must be kept out of the reach of children.
The shelf life of Chondartron-gel, subject to storage conditions, is 2 years from the date of manufacture.
No special precautions are required when disposing of unused medicinal product.
Hondartron-gel is produced in plastic bottles or 500 ml tubes.
from 0 to +25
for the treatment of cattle, horses and dogs with diseases of the musculoskeletal system.