RENEFIL LIGHT PLUS

RENEFIL LIGHT PLUS is a soft-texture dermal filler formulated with cross-linked hyaluronic acid (HA), polynucleotides (PN), and lidocaine for superficial injection into areas with fine lines, mild volume loss, and skin texture irregularities. It is ideal for the periorbital area, fine perioral lines, forehead, temples, and neck, providing subtle enhancement, hydration, and collagen regeneration. The combination of HA and PN delivers both immediate smoothing effects and long-term skin revitalization, while the addition of 0.3% lidocaine ensures a more comfortable procedure. RENEFIL LIGHT PLUS offers excellent tissue integration with low viscosity, making it an ideal choice for natural-looking refinement.

• Indicated for: Fine lines, surface-level wrinkles, early skin laxity
• Texture: Soft, smooth, and highly spreadable
• Mechanism: Volumization + dermal biostimulation
• Duration of effect: Up to 9–12 months

RENEFIL LIGHT PLUS is administered via superficial to mid-dermal injection, using a 30G needle. Its rheological properties allow for smooth application, even spread, and low injection force.

• Injection depth: Superficial to mid dermis
• Needle size: 30G, usually included in package
• Injection techniques: Linear threading, serial puncture, or microdroplet
• Treatment areas: Crow’s feet, fine forehead lines, tear trough, smoker’s lines, neck lines
• Pain management: Contains 0.3% lidocaine
• Procedure time: Around 15–25 minutes

RENEFIL LIGHT PLUS is indicated for fine line correction, hydration, and skin texture improvement in patients seeking subtle rejuvenation. It is ideal for sensitive areas where softer fillers are required.

Indications:

• Crow’s feet
• Perioral lines
• Neck and décolletage rejuvenation
• Tear trough correction
• Superficial wrinkles and creases

Contraindications:

• Known allergy to HA, lidocaine, or polynucleotides
• Pregnancy or breastfeeding
• Active infection or inflammation at treatment site
• Autoimmune disorders
• History of severe allergic reactions

Side Effects:

• Redness, swelling, or mild bruising
• Tenderness or itching
• Rare: Nodule formation, hypersensitivity, infection

RENEFIL LIGHT PLUS combines hydrating and regenerating agents in a balanced formulation tailored for delicate areas and superficial lines.

• Cross-linked Hyaluronic Acid (HA): 20 mg/mL
• Polynucleotides (PN): 1.875 mg/mL
• Lidocaine HCl: 0.3% (3 mg/mL)
• Form: Transparent, sterile, viscoelastic gel
• pH and osmolarity: Physiologically balanced

RENEFIL LIGHT PLUS is provided in a ready-to-use syringe, along with sterile accessories required for treatment.

• 1 prefilled syringe with 1 mL of RENEFIL LIGHT PLUS
• 2 sterile 30G needles
• Traceability stickers for patient records
• IFU (Instructions for use)
• Sterile, tamper-proof blister packaging

RENEFIL LIGHT PLUS has a very favorable safety profile, particularly when used with proper injection technique. Most side effects are mild and transient.

Common Side Effects:

• Localized swelling, bruising, or redness
• Minor tenderness or tightness
• Itching in sensitive skin types

Rare Side Effects:

• Delayed nodules
• Allergic reaction to lidocaine or PN
• Skin discoloration
• Vascular occlusion (extremely rare with proper injection depth)

Proper storage is essential to preserve the sterility and viscosity of RENEFIL LIGHT PLUS.

• Storage temperature: 2°C to 25°C (36°F to 77°F)
• Avoid freezing
• Keep away from light and heat
• Store in sealed original packaging
• Single-use only – discard any unused product