Teosyal® RHA Kiss Lidocaine

General Information

TEOSYAL® RHA KISS LIDOCAINE is a sterile, injectable hyaluronic acid-based dermal filler manufactured by TEOXANE Laboratories in Switzerland. It is specifically developed for lip enhancement, lip contouring and the correction of fine lines around the mouth while maintaining natural-looking facial expressions.

The formulation contains 23 mg/mL of cross-linked hyaluronic acid of non-animal origin, developed using Resilient Hyaluronic Acid (RHA) technology. This technology helps the gel adapt to natural lip movements, providing flexibility and dynamic-looking results.

The product also contains 0.3% lidocaine hydrochloride (3 mg/mL), a local anaesthetic that helps reduce discomfort during treatment.

TEOSYAL® RHA KISS LIDOCAINE is particularly suitable for adding subtle lip volume, improving lip definition and correcting perioral wrinkles. Its flexible formulation supports natural-looking lip enhancement without compromising facial expressions.

Indications for TEOSYAL® RHA KISS LIDOCAINE

TEOSYAL® RHA KISS LIDOCAINE is designed to enhance lip appearance and correct wrinkles around the mouth. Its aesthetic applications include:

• Enhancement of lip volume and fullness.
• Definition and reshaping of the lip contour.
• Improvement of lip symmetry.
• Correction of fine perioral lines.
• Subtle lip augmentation.
• Improvement of lip appearance and definition.
• Natural-looking lip rejuvenation.

The product is intended for injection into the appropriate lip tissue or dermal layer by appropriately trained healthcare professionals, following the manufacturer’s instructions.

Contraindications and Precautions

TEOSYAL® RHA KISS LIDOCAINE should not be used in individuals with known hypersensitivity to hyaluronic acid, lidocaine or amide-type local anaesthetics.

Treatment should be avoided in cases of active skin infections or inflammation, severe allergies, autoimmune diseases, immunodeficiency, bleeding disorders or a tendency to develop keloid scars. Use during pregnancy or breastfeeding and in individuals under 18 years of age should follow the manufacturer’s instructions and applicable medical guidance.

Medical assessment is required before treatment, particularly for patients with cardiac conditions, epilepsy or porphyria. The product must never be injected into blood vessels and should only be administered by appropriately trained healthcare professionals.

Potential Side Effects

Temporary reactions may include redness, swelling, bruising, tenderness, itching, pain and small lumps around the injection site.

Less common complications include infection, persistent inflammation, nodules, skin discolouration and hypersensitivity reactions.

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

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