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BELLAST PLUS 01
BELLAST®

BELLAST® PLUS

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For professional use only.

Manufacturer: DongkookPharma Co. Ltd.
Active Substance(s): CROSS LINKED HYALURONIC ACID, LIDOCAINE
Strength: 24mg/ml HA, 0.3% Lidocaine
Pack Size: 1 x 1ml Pre-Filled Syringe, 2 x 27G Needles
Bellast PLUS contains Lidocaine, which makes dermal filling painless for patients. It is injected into the mid to deep dermis layer of the skin for moderate to severe facial wrinkles and folds, such as nasolabial folds. It’s also good for defining face features like the nasal bridge, chin, and cheekbones.

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INFORMATION

BELLAST® PLUS Product Description

BELLAST® PLUS is a hyaluronic acid-based dermal filler designed for wrinkle improvement, facial contouring, and volume restoration. Its formulation includes 20 mg of cross-linked hyaluronic acid per 1 mL pack, ensuring non-animal origin, high biocompatibility, and natural degradation over time. This product does not contain lidocaine.

BELLAST® PLUS Key Features and Benefits

BELLAST® PLUS is distinguished by its HCXL (High Concentration Cross-Linking) Technology, offering increased purity and reduced residual cross-linker content for enhanced safety. Key benefits include:

  • Hydration improvement and skin rejuvenation.
  • Long-lasting effects for up to six months, depending on the injection site and patient’s condition.
  • Balanced combination of viscosity and elasticity, ensuring cohesiveness and resistance to external forces.

Clinical studies validate its efficacy and safety, showing significant wrinkle improvement without severe adverse events.

BELLAST® PLUS Composition

The key active ingredient in BELLAST® PLUS is 20 mg of cross-linked hyaluronic acid per 1 mL. This monophasic filler provides high cohesiveness and optimal elasticity for long-lasting results.

BELLAST® PLUS Intended Purpose / Indications

BELLAST® PLUS is designed for:

  • Treating medium to deep facial wrinkles, including nasolabial folds and marionette lines.
  • Restoring facial volume in areas like the cheeks and chin.
  • Enhancing facial contours and overall skin hydration.

BELLAST® PLUS Injection and Treatment Areas

This filler is recommended for:

  • Injection into the mid-dermis layer for medium to deep wrinkles.
  • Ideal for addressing areas such as:
    • Nasolabial folds
    • Marionette lines
    • Cheek augmentation

BELLAST® PLUS Reconstitution and Preparation Guidelines

Preparation involves aseptic handling to ensure safety. While no additional dilution is needed due to the ready-to-use formulation, practitioners should follow standard protocols for syringe handling and needle attachment.

BELLAST® PLUS Administration and Dosage

Administered by trained professionals, the recommended techniques include:

  • Linear threading for wrinkle filling.
  • Fan or cross-hatching techniques for volumization. Dosage varies by area but should not exceed 1 mL per session for optimal safety and efficacy.

BELLAST® PLUS Storage Instructions

Store BELLAST® PLUS in a controlled environment:

  • Temperature: 2–25°C.
  • Avoid exposure to light and freezing conditions to maintain product integrity.

BELLAST® PLUS Contraindications

BELLAST® PLUS should not be used in:

  • Patients with allergies to hyaluronic acid or previous filler treatments.
  • Areas with active skin infections or inflammation.
  • Individuals with autoimmune disorders or during pregnancy.

BELLAST® PLUS Precautions and Warnings

Important considerations include:

  • Avoid intravascular injection to prevent complications.
  • Conduct a thorough medical history review to rule out contraindications.
  • Avoid combining with other dermal treatments during the same session.

BELLAST® PLUS Post-Treatment Care

Patients should:

  • Refrain from applying makeup for at least 24 hours post-treatment.
  • Avoid UV exposure and extreme temperatures for 72 hours.
  • Use gentle skin care products to prevent irritation.

BELLAST® PLUS Side Effects and Adverse Reactions

Mild side effects include:

  • Redness, swelling, or bruising at the injection site.
  • Transient discomfort, typically resolving within a few days. No serious adverse events were reported in clinical trials.

BELLAST® PLUS Patient Eligibility

Suitable for adults seeking:

  • Wrinkle reduction or facial contour improvement.
  • Volume restoration in targeted areas. Patients with health conditions affecting healing or skin integrity may require further assessment.

BELLAST® PLUS Follow-Up and Maintenance

To maintain results:

  • Follow-up treatments every 4–6 months are recommended.
  • Frequency depends on the patient’s skin type and area treated.

BELLAST® PLUS Manufacturer and Regulatory Information

Produced by BELLAST, the product complies with global safety standards and features CE certification. Each unit includes a unique batch code and expiration date for traceability.

BELLAST® PLUS FAQ

Q: How long does the effect last? A: Results typically last 4–6 months, varying by treatment area and patient factors.

Q: Is the treatment painful? A: While lidocaine-free, discomfort is minimal due to professional administration techniques.

Q: Who is not a candidate for this treatment? A: Patients with allergies, autoimmune diseases, or active skin infections should avoid the treatment.

 

BELLAST® PLUS Product Description

BELLAST® PLUS is a hyaluronic acid-based dermal filler designed for wrinkle improvement, facial contouring, and volume restoration. Its formulation includes 20 mg of cross-linked hyaluronic acid per 1 mL pack, ensuring non-animal origin, high biocompatibility, and natural degradation over time. This product does not contain lidocaine.

BELLAST® PLUS Key Features and Benefits

BELLAST® PLUS is distinguished by its HCXL (High Concentration Cross-Linking) Technology, offering increased purity and reduced residual cross-linker content for enhanced safety. Key benefits include:

  • Hydration improvement and skin rejuvenation.
  • Long-lasting effects for up to six months, depending on the injection site and patient’s condition.
  • Balanced combination of viscosity and elasticity, ensuring cohesiveness and resistance to external forces.

Clinical studies validate its efficacy and safety, showing significant wrinkle improvement without severe adverse events.

BELLAST® PLUS Composition

The key active ingredient in BELLAST® PLUS is 20 mg of cross-linked hyaluronic acid per 1 mL. This monophasic filler provides high cohesiveness and optimal elasticity for long-lasting results.

BELLAST® PLUS Intended Purpose / Indications

BELLAST® PLUS is designed for:

  • Treating medium to deep facial wrinkles, including nasolabial folds and marionette lines.
  • Restoring facial volume in areas like the cheeks and chin.
  • Enhancing facial contours and overall skin hydration.

BELLAST® PLUS Injection and Treatment Areas

This filler is recommended for:

  • Injection into the mid-dermis layer for medium to deep wrinkles.
  • Ideal for addressing areas such as:
    • Nasolabial folds
    • Marionette lines
    • Cheek augmentation

BELLAST® PLUS Reconstitution and Preparation Guidelines

Preparation involves aseptic handling to ensure safety. While no additional dilution is needed due to the ready-to-use formulation, practitioners should follow standard protocols for syringe handling and needle attachment.

BELLAST® PLUS Administration and Dosage

Administered by trained professionals, the recommended techniques include:

  • Linear threading for wrinkle filling.
  • Fan or cross-hatching techniques for volumization. Dosage varies by area but should not exceed 1 mL per session for optimal safety and efficacy.

BELLAST® PLUS Storage Instructions

Store BELLAST® PLUS in a controlled environment:

  • Temperature: 2–25°C.
  • Avoid exposure to light and freezing conditions to maintain product integrity.

BELLAST® PLUS Contraindications

BELLAST® PLUS should not be used in:

  • Patients with allergies to hyaluronic acid or previous filler treatments.
  • Areas with active skin infections or inflammation.
  • Individuals with autoimmune disorders or during pregnancy.

BELLAST® PLUS Precautions and Warnings

Important considerations include:

  • Avoid intravascular injection to prevent complications.
  • Conduct a thorough medical history review to rule out contraindications.
  • Avoid combining with other dermal treatments during the same session.

BELLAST® PLUS Post-Treatment Care

Patients should:

  • Refrain from applying makeup for at least 24 hours post-treatment.
  • Avoid UV exposure and extreme temperatures for 72 hours.
  • Use gentle skin care products to prevent irritation.

BELLAST® PLUS Side Effects and Adverse Reactions

Mild side effects include:

  • Redness, swelling, or bruising at the injection site.
  • Transient discomfort, typically resolving within a few days. No serious adverse events were reported in clinical trials.

BELLAST® PLUS Patient Eligibility

Suitable for adults seeking:

  • Wrinkle reduction or facial contour improvement.
  • Volume restoration in targeted areas. Patients with health conditions affecting healing or skin integrity may require further assessment.

BELLAST® PLUS Follow-Up and Maintenance

To maintain results:

  • Follow-up treatments every 4–6 months are recommended.
  • Frequency depends on the patient’s skin type and area treated.

BELLAST® PLUS Manufacturer and Regulatory Information

Produced by BELLAST, the product complies with global safety standards and features CE certification. Each unit includes a unique batch code and expiration date for traceability.

BELLAST® PLUS FAQ

Q: How long does the effect last? A: Results typically last 4–6 months, varying by treatment area and patient factors.

Q: Is the treatment painful? A: While lidocaine-free, discomfort is minimal due to professional administration techniques.

Q: Who is not a candidate for this treatment? A: Patients with allergies, autoimmune diseases, or active skin infections should avoid the treatment.

 

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