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Information about the drug, given in this section is intended for medical and pharmaceutical professionals and should not be used for self-treatment. Information given to familiarize with the basic properties of the drug and cannot be considered as official.
This medicine specially designed to correct moderate wrinkles and folds and is successfully used for glabellar and nasolabial folds, wrinkles on the nose.
Restylane was the first drug based on Hyaluronic acid, approved by the American Management on sanitary inspection behind quality of foodstuff and medicines.
Tool specially designed to correct moderate wrinkles and folds and is successfully used for glabellar and nasolabial folds, wrinkles on the nose. Restylane is widely used in the correction of the volume and contour of the lips and to correct facial wrinkles that are formed when you smile and wrinkles "puppets".
Due to its unique properties, in addition to instant correction tissue volume Restyalne has the ability to stimulate the production of collagen in the skin, which enhances and extends the natural rejuvenating effect on the procedure. This fact was confirmed by a group of scientists in the clinical research process (Wang F, Garza LA, Kang S, Varani J, Orringer JS, Fisher GJ, Voorhees JJ. In vivo stimulation of de novo collagen production caused by crossed-linked hyaluronic acid dermal ller injections in photodamaged human skin. Arch Dermatol 2007 Feb; 143(2):155-63).
The name of the medical product: Material biopolymer Restylane Vital Light, sterile, single use
The hyaluronic acid stabilized on 12 mg/ml in the syringe 1 PC.
The injection needle 30G x ½ - 3 PCs.
Instruction manual - 1 PC.
The hyaluronic acid stabilized: 12mg/ml
Phosphate buffer solution: Hon. PK
Restylane Vital Light is a sterile, transparent gel of stabilized hyaluronic acid of non-animal origin. The Restylane Vital Light is supplied in a glass syringe with a tip of Luer. The contents of the syringe sterilized by autoclaving. The drug is intended for single use only. To each syringe attached disposable sterile needles. Information on the method of sterilization and the size of needle is marked on their packaging. Number of pieces in the package and the amount of drug in each syringe is indicated on the outer packaging. Sticker for attachment to the patient's medical record is part of the label of the syringe. This label should nucleii to the patient record to enable identification of the drug.
Restylane Vital Light is designed to restore the balance of fluids in the skin, improve its texture and elasticity. It should be administered by injection into the dermal layer of the skin.
Restylane Vital Light is only for injection into the dermis.
Do not enter into the blood vessels. Intravascular injection of these drugs, like other injectable drugs for medical purposes, can lead to blockage of blood vessels, ischemia and necrosis.
When blanching of the skin over the injection site should immediately discontinue the drug and massaging the skin to restore its normal color.
Should not be administered this drug to patients with bleeding disorders, as well as receiving thrombolytics or anticoagulants.
Do not expose Restylane Vital Light is re-sterilized.
Do not mix with other drugs prior to injection of the implant.
General provisions relating to the injection of medical preparations
Injection procedures are associated with risk of infection. You should observe the rules of asepsis and execute standard procedures for the prevention of transmission.
You should be very careful in areas immediately adjacent to permanent implants or vulnerable formations, e.g., nerves, blood vessels and other vital structures.
This drug should not be installed in areas of active skin diseases, e.g., inflammation, infection, or tumor, and also in adjacent areas of the skin.
Special care is needed with the introduction of the drug in close proximity to permanent implants.