Revolax™ Deep Lidocaine

General Information

REVOLAX™ DEEP LIDOCAINE is a sterile, injectable hyaluronic acid-based dermal filler manufactured by Across Co., Ltd. in South Korea. It is specifically designed to correct deep facial wrinkles and folds, restore lost facial volume and enhance facial contours while providing natural-looking results.

The formulation contains 24 mg/mL of cross-linked hyaluronic acid of non-animal origin, combined with 0.3% lidocaine hydrochloride (3 mg/mL) to help reduce discomfort during treatment. It also contains phosphate-buffered saline to maintain formulation stability.

REVOLAX™ DEEP LIDOCAINE features a thick, highly cohesive gel with high viscoelasticity, making it suitable for deeper wrinkles, facial volume restoration and contour enhancement.

Indications for REVOLAX™ DEEP LIDOCAINE

REVOLAX™ DEEP LIDOCAINE is designed to correct deep wrinkles and restore facial volume. Its aesthetic applications include:

• Correction of deep nasolabial folds.
• Treatment of marionette lines.
• Improvement of deep facial wrinkles and folds.
• Restoration of cheek and cheekbone volume.
• Enhancement of chin projection.
• Definition and contouring of the jawline.
• Lip augmentation and contour enhancement.
• Correction of facial volume deficiencies.
• Improvement of facial symmetry and contours.

The product is intended for injection into the mid-to-deep dermis or subcutaneous tissue, depending on the treatment indication, by an appropriately trained healthcare professional following the manufacturer’s instructions.

Contraindications and Precautions

REVOLAX™ DEEP LIDOCAINE 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 cases of active skin infections or inflammation, severe allergies, previous anaphylactic reactions or a tendency to develop hypertrophic scars. Use during pregnancy or breastfeeding should follow the manufacturer’s instructions and applicable medical guidance.

A medical assessment is required before treatment. 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, granulomas, 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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