RENEFIL LIGHT PLUS

RENEFIL LIGHT PLUS Product Description

RENEFIL LIGHT PLUS is a specialized dermal filler based on hyaluronic acid, uniquely formulated with cross-linked Hyaluronic Acid (HA), Polynucleotide (PN), and Lidocaine. Specifically created to address moderate facial wrinkles and contour enhancements, it ensures hydration, elasticity improvement, and patient comfort due to the presence of lidocaine.

RENEFIL LIGHT PLUS Key Features and Benefits

RENEFIL LIGHT PLUS effectively addresses moderate wrinkles, providing noticeable improvements in skin elasticity, hydration, and smoothness. Its formulation stimulates collagen production, resulting in rejuvenated skin texture and structure.

• Effective wrinkle correction
• Improved skin elasticity and hydration
• Promotes collagen synthesis
• Comfortable injections with Lidocaine

RENEFIL LIGHT PLUS Composition

RENEFIL LIGHT PLUS includes carefully balanced active ingredients:

• Cross-Linked Hyaluronic Acid: 20 mg/mL
• Polynucleotide (PN): 1.875 mg/mL
• Lidocaine HCl: 3.0 mg (0.3%) These active ingredients contribute to volume restoration, skin regeneration, and reduced discomfort during procedures.

RENEFIL LIGHT PLUS Intended Purpose / Indications

RENEFIL LIGHT PLUS is indicated for moderate wrinkle treatment and facial contouring. It effectively addresses mid-depth wrinkles and enhances contours in areas such as nasolabial folds, lips, chin, and forehead.

• Moderate wrinkle treatment
• Facial contour enhancements
• Lip volume augmentation

RENEFIL LIGHT PLUS Injection and Treatment Areas

The filler is intended for injection into mid-dermal to superficial subcutaneous layers, suitable for addressing moderate wrinkles and subtle contouring. Recommended treatment areas include nasolabial folds, lips, forehead, chin, and nose.

• Mid-dermal/superficial subcutaneous injection
• Nasolabial folds, lips, forehead, chin, nose

RENEFIL LIGHT PLUS Reconstitution and Preparation Guidelines

RENEFIL LIGHT PLUS is supplied ready-to-use in a sterile pre-filled syringe. No dilution is required. Always practice aseptic handling, ensure the syringe is free from air bubbles, and maintain sterile conditions during the procedure.

• Ready-to-use
• No dilution needed
• Aseptic handling essential

RENEFIL LIGHT PLUS Administration and Dosage

RENEFIL LIGHT PLUS should be administered by certified professionals. Dosage generally ranges from 0.5 to 2.0 mL per area, tailored to the treatment objectives. Careful, gradual injection technique is crucial for optimal results and patient comfort.

• Dosage: 0.5-2.0 mL per area
• Gradual injection recommended

RENEFIL LIGHT PLUS Storage Instructions

Proper storage conditions are vital to maintain product integrity. Store RENEFIL LIGHT PLUS at temperatures between 2–25°C, protected from direct sunlight, and never freeze. Use immediately after opening to maintain sterility.

• Store at 2–25°C
• Protect from sunlight
• Avoid freezing

RENEFIL LIGHT PLUS Contraindications

Avoid using RENEFIL LIGHT PLUS in patients with allergies to hyaluronic acid, lidocaine, or filler components, active infections, autoimmune disorders, inflammatory skin conditions, or during pregnancy and lactation.

• Allergies to filler components
• Active skin infections or inflammation
• Pregnancy or breastfeeding

RENEFIL LIGHT PLUS Precautions and Warnings

Extreme caution is advised to prevent intravascular injection, reducing the risk of vascular complications. RENEFIL LIGHT PLUS should not be combined with other dermal fillers at the same injection site. Thorough patient evaluation and medical history assessment are critical.

• Avoid intravascular injections
• Do not mix with other fillers

RENEFIL LIGHT PLUS Post-Treatment Care

Post-procedure guidelines include avoiding makeup application for 24 hours, minimizing UV exposure, and refraining from extreme heat or cold (such as saunas) for a week to support healing and minimize side effects.

• Avoid makeup for 24 hours
• Limit UV exposure
• Avoid extreme temperatures for one week

RENEFIL LIGHT PLUS Side Effects and Adverse Reactions

Typical reactions post-treatment include mild redness, swelling, bruising, or tenderness at injection sites. Serious side effects are rare but should be reported immediately, including prolonged swelling, severe pain, or signs of infection.

• Mild reactions: redness, swelling, bruising
• Report severe reactions promptly

RENEFIL LIGHT PLUS Patient Eligibility

Suitable patients for RENEFIL LIGHT PLUS are adults aged 18-65 experiencing moderate wrinkles or seeking subtle facial enhancements. Patients should be healthy and have no conditions contraindicating dermal filler use.

• Age 18-65
• Moderate wrinkles and subtle enhancement
• Good general health required

RENEFIL LIGHT PLUS Follow-Up and Maintenance

Patients should schedule an initial follow-up 4 weeks after treatment for outcome evaluation. Maintenance treatments every 6-9 months are recommended to sustain results.

• Follow-up at 4 weeks
• Maintenance every 6-9 months

RENEFIL LIGHT PLUS Manufacturer and Regulatory Information

Manufactured by BMI Korea Co., Ltd., RENEFIL LIGHT PLUS adheres to international quality standards, including ISO 13485:2016, and holds CE certification, ensuring product reliability and patient safety.

• Manufacturer: BMI Korea Co., Ltd.
• Regulatory compliance: ISO 13485, CE certified

RENEFIL LIGHT PLUS FAQ

How quickly are results visible with RENEFIL LIGHT PLUS? Immediate improvement after treatment with progressive enhancement over time.

Does RENEFIL LIGHT PLUS injection hurt? Inclusion of lidocaine significantly reduces discomfort during the injection process.

How long do RENEFIL LIGHT PLUS effects last? Results typically last between 6-9 months.

Are normal activities permissible immediately post-treatment? Routine activities can resume immediately, but strenuous activities should be avoided for 24-48 hours post-treatment.