BELLAST® L Product Description

BELLAST® L is a premium hyaluronic acid-based dermal filler designed to address medium-to-deep facial wrinkles and enhance skin volume. It includes 20 mg of cross-linked hyaluronic acid and 3 mg of lidocaine hydrochloride, providing effective treatment with pain relief. The product is of non-animal origin, ensuring biocompatibility and natural degradation over time.

The Bellast dermal filler L Series, developed by South Korea’s Dongkook Pharmaceutical, is part of an advanced collection of medical devices aimed at facial rejuvenation. This hyaluronic acid-based filler features a multi-reticulated gel specifically designed to enhance facial aesthetics, particularly for lip augmentation.

BELLAST Filler Key Features and Benefits

BELLAST® L offers a high-purity hyaluronic acid hydrogel through HCXL technology (High Concentration Cross-Linking). This process minimizes cross-linking agents, ensuring safety and reducing risks of side effects. Its advanced formulation provides benefits:

• Enhanced skin hydration and elasticity.
• Long-lasting results, with effects lasting up to six months depending on treatment areas and individual conditions.
• Ideal viscosity-to-elasticity ratio (3:1) for improved cohesiveness and resistance to external forces, reducing risks such as gel migration.
• Versatility for treating various facial wrinkles and enhancing facial features, particularly lips.

BELLAST® L Composition

Dongkook Pharmaceutical meticulously created the BELLAST collection of dermal fillers to address multiple aesthetic concerns. Notably, the composition of BELLAST® L is as follows:

• Hyaluronic Acid: 20 mg of cross-linked hyaluronic acid for volume restoration.
• Lidocaine Hydrochloride: 3 mg for local anesthetic properties, ensuring patient comfort during application.

BELLAST® L Intended Purpose / Indications

Moreover, BELLAST increased the youthful look and natural appearance of individuals who have undergone this treatment. The manufacturer designed this dermal filler to treat moderate-to-severe facial wrinkles and folds, including:

• Nasolabial folds
• Glabellar lines
• Lip volume and contour
• Other facial areas that require a reduction in aging signs and volume and contour enhancements

While maintaining safety and efficacy, BELLAST L can deliver natural-looking and long-lasting results to suitable patients.

BELLAST® L Injection and Treatment Areas

A licensed aesthetic provider should only administer BELLAST L injections to ensure safety and efficacy. These injections typically utilize a fine needle or cannula, targeting the superficial or mid-dermis for uniform distribution and optimal results, making it suitable for:

• Aging lines
• Medium-to-deep wrinkles
• Lip augmentation

BELLAST® L Reconstitution and Preparation Guidelines

BELLAST® L is pre-filled in sterile syringes, eliminating the need for reconstitution. Healthcare professionals must adhere to the recommended preparation for BELLAST dermal fillers, which the key preparation steps include:

• Ensure aseptic conditions when handling and administering.
• Use appropriate tools like 27G or 30G needles for injection.
• Store at 2–25°C, avoiding freezing or exposure to direct light.

BELLAST® L Administration and Dosage

Each BELLAST L package comes with a pre-filled syringe containing 1 ml of hyaluronic acid (20 mg). The exact dosage, however, may vary based on the patient’s treatment goals and the required level of correction. Furthermore, administered by trained professionals, the typical injection technique involves:

• A slow injection to the mid-dermis layer.
• Properly and gently massage the treatment area post-injection to ensure even distribution.
• Maximum injection volume depends on the treatment area, with precise dosages tailored to patient needs.

However, some BELLAST injections may require deep dermis injection. This highlights that medical professionals should be trained and equipped with comprehensive knowledge about dermal filler injections to administer these appropriately and safely to patients.

BELLAST® L Storage Instructions

To maintain efficacy, BELLAST® L must be stored at:

• Temperatures between 2–25°C.
• Away from direct sunlight and freezing conditions.
• In its original sterile packaging until use.

BELLAST® L Contraindications

The use of BELLAST® L is contraindicated in the following cases:

• Known allergies to hyaluronic acid or lidocaine.
• Patients with active skin infections or inflammatory conditions near the treatment site.
• Pregnant or breastfeeding individuals.
• Patients with autoimmune diseases or impaired healing.

BELLAST® L Precautions and Warnings

Professionals should consider:

• Avoiding intravascular injection to prevent complications.
• Not combining with other cosmetic procedures in the same session.
• Conducting allergy testing when uncertain about sensitivity.

BELLAST® L Post-Treatment Care

Patients should follow these aftercare recommendations of healthcare professionals to minimize discomfort and support recovery:

• Apply ice packs or cold compresses to the treated area.
• To reduce swelling and bruising, avoid strenuous activities for 24 hours.
• Stay adequately hydrated and refrain from massaging or frequently touching the injection site.
• Report any unusual reactions to the practitioner immediately.

BELLAST® L Side Effects and Adverse Reactions

Despite their favorable safety profile, BELLAST fillers may cause potential risks. Patients may experience temporary reactions at the injection site, which typically subside within a few days to a week. Rare but severe reactions may also occur and may require immediate medical attention for appropriate management.

• Temporary redness, swelling, or bruising at the injection site.
• Rare but potential adverse events like infection or allergic reactions.

While various clinical trials reported mild and transient reactions with no severe adverse effects, practitioners must equip patients with comprehensive information about the risks and explain how to recognize and report unusual symptoms.

BELLAST® L Patient Eligibility

BELLAST® L is suitable for:

• Patients over 18 years of age with moderate-to-severe wrinkles.
• Individuals in good general health with no underlying contraindicated conditions.

It is not suitable for patients who have any contraindications. You should avoid administering BELLAST L to individuals with hypersensitivity to its components.

BELLAST® L Follow-Up and Maintenance Results

Treatment results last approximately 6 months, depending on individual factors. Follow-up sessions are recommended to maintain optimal outcomes. Practitioners may suggest:

• A review session at 3–4 months post-treatment for touch-ups.
• Regular maintenance to achieve consistent results.

BELLAST® L Manufacturer and Regulatory Information

BELLAST® L is manufactured under strict regulatory compliance, ensuring safety and efficacy. It adheres to CE marking standards for medical devices and comes with unique batch codes for traceability.

BELLAST® L FAQ

Q: How long do results last? A: Results last up to 6 months, depending on the area treated and individual metabolism.

Q: Is the procedure painful? A: The inclusion of lidocaine ensures minimal discomfort during treatment.

Q: Who can administer BELLAST® L? A: Only trained medical professionals should perform injections to ensure safety and effectiveness.