Teosyal® PureSense Redensity I

General Information

TEOSYAL® PURESENSE REDENSITY I is a sterile, injectable skin-quality treatment manufactured by TEOXANE Laboratories in Switzerland. It is formulated to improve skin hydration, elasticity and radiance while helping reduce the appearance of fine lines and early signs of skin ageing.

The formulation contains 15 mg/mL of non-cross-linked hyaluronic acid combined with a dermo-restructuring complex of amino acids, antioxidants, minerals and vitamin B6. Hyaluronic acid helps attract and retain moisture in the skin, while the additional ingredients are intended to support skin quality and revitalisation.

The product also contains 0.3% lidocaine hydrochloride (3 mg/mL) to help reduce discomfort during treatment.

Unlike conventional volumising dermal fillers, TEOSYAL® PURESENSE REDENSITY I is primarily intended for skin hydration and revitalisation rather than significant facial volume enhancement.

Pack contents:

• 1 pre-filled syringe of 3 mL
• Sterile injection accessories, according to the supplied pack
• Product instructions and traceability labels

Indications for TEOSYAL® PURESENSE REDENSITY I

TEOSYAL® PURESENSE REDENSITY I is designed to improve overall skin quality and hydration. Its aesthetic applications include:

• Hydration of dehydrated skin
• Improvement of skin radiance and luminosity
• Reduction in the appearance of fine lines
• Improvement of skin elasticity and smoothness
• Revitalisation of the face, neck and décolleté
• Improvement of skin texture and overall skin appearance

The product is intended for superficial intradermal injection by a qualified healthcare professional, following the manufacturer’s instructions and an appropriate treatment plan.

Contraindications and Precautions

TEOSYAL® PURESENSE REDENSITY I should not be used in individuals with known hypersensitivity to hyaluronic acid, lidocaine or any other component of the formulation. Treatment should be avoided in areas affected by active skin infections or inflammation.

Careful medical assessment is required for individuals with a history of severe allergies, autoimmune conditions, bleeding disorders or relevant medical conditions. Use during pregnancy or breastfeeding and in minors should follow the manufacturer’s instructions and applicable 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, itching, pain and small bumps at the injection site. These reactions generally resolve over time.

Less common complications may include persistent inflammation, infection, nodules or hypersensitivity reactions. Rare but serious injection-related complications include vascular occlusion, tissue damage and skin necrosis. Severe pain, unusual skin colour changes or visual disturbances following treatment require immediate medical attention.

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