Teosyal® Puresense Deep Lines

General Information

TEOSYAL® PURESENSE DEEP LINES is a sterile, injectable dermal filler manufactured by TEOXANE Laboratories in Switzerland. It is formulated with cross-linked hyaluronic acid of non-animal origin and designed to correct deep facial wrinkles, restore lost volume and improve the appearance of pronounced skin folds.

The formulation contains 25 mg/mL of cross-linked hyaluronic acid and 3 mg/mL of lidocaine hydrochloride (0.3%) in a phosphate buffer solution. Hyaluronic acid helps restore volume and smooth deep wrinkles, while lidocaine is a local anaesthetic that helps reduce discomfort during injection.

Its viscoelastic gel consistency is designed for the correction of pronounced facial lines. The product is intended for injection into the deep dermis by a qualified healthcare professional, in accordance with the manufacturer’s instructions.

Indications for TEOSYAL® PURESENSE DEEP LINES

TEOSYAL® PURESENSE DEEP LINES is designed for filling deep facial wrinkles and restoring volume in selected areas. Its intended aesthetic applications include:

• Deep nasolabial folds
• Marionette lines
• Pronounced facial creases
• Deep skin depressions
• Cheek augmentation
• Facial contour and oval reshaping

The product may also be used for selected volume-restoration procedures when clinically appropriate. Treatment areas, injection depth and technique must be determined by a qualified practitioner according to the product’s approved instructions.

Contraindications and Precautions

TEOSYAL® PURESENSE DEEP LINES should not be used in individuals with known hypersensitivity to hyaluronic acid, lidocaine or other amide-type local anaesthetics, or any other product component.

Injection should be avoided in areas affected by active skin infections or inflammation. Particular medical assessment is required for patients with a history of severe allergies, autoimmune disorders, bleeding disorders or other relevant medical conditions. Use during pregnancy or breastfeeding and in minors should be avoided unless specifically permitted by applicable product instructions and medical guidance.

The product must not be injected into blood vessels. It should only be administered by appropriately trained healthcare professionals.

Potential Side Effects

Temporary reactions may include redness, swelling, bruising, tenderness, pain, itching and small lumps around the injection site. These reactions are generally mild and resolve over time.

Rare but serious complications can include infection, vascular occlusion, tissue damage, skin necrosis and visual disturbances, including blindness. Severe or unusual pain, changes in skin colour or vision problems following treatment require immediate medical attention.

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