Chondromarin^®

The number of National Certificate of Registration: 77.99.23.3.U.38.1.07 dated January 10, 2007

Specification number: TU 9283-004-59230155-07

Formulation: “Dienai C”  (salmon roe extract (low-molecular DNA), potato starch, microcrystalline cellulose, sodium chloride, polyethylene glycol), dried milled cartilage of salmon.

Pharmacological group: refers to the group of food supplements-parapharmaceutics.

Toxicologic characteristics: This preparation refers to class 4 (“low-hazard substances”) according to Russian Interstate Standard 12.1.007-76. No toxic or side effects were revealed after the experimental intragastral administration to animals.

Indications: arthritis and polyarthritis, osteoarthrosis, osteochondrosis, injuries of the locomotorium, sclerodermatitis, oncologic conditions.

Administration method and dosage: orally, take 1 capsule three times a day during the meal to adults and children older than 14 years. Administration duration is three weeks.

Contraindications: individual intolerance for preparation components, pregnancy, lactation. It is used with caution in patients with threat of hemorrhage from the esophageal veins and bleeding gastric ulcer, in patients after vascular crisis.

Pharmaceutical form: 0.5 g capsules, 70 (30) per package.

Storing conditions: store in a dry place away from light, out of the reach of children at temperature up to 25 oC.

Expiration date: 11 months from the date of manufacturing.

Prescription conditions: No prescription required.

Manufacturer: Siberian Center for Pharmacology and Biotechnology, closed joint-stock company (Novosibirsk, Russian Federation).