REVANESSE® ULTRA+ Lidocaine

Where can I buy this product?

Revanesse® Ultra+ Lidocaine is available for purchase through Health Supplies Plus by licensed medical practitioners holding a valid medical license. First-time buyers can register an online account by providing required professional information, including medical license verification and a valid shipping address. Account verification is typically completed within 2 business hours, after which you can purchase medical supplies at competitive wholesale pricing. Registered members may also be eligible for volume discounts and receive dedicated customer service support. We are committed to ensuring all products are sourced and sold exclusively to qualified professionals.

Product Information

What is REVANESSE® Ultra+ Lidocaine?

REVANESSE® Ultra+ Lidocaine is a high-viscosity, sterile, cross-linked hyaluronic acid (HA) dermal filler manufactured by Prollenium Medical Technologies Inc. Engineered with Prollenium’s Thixofix® cross-linking technology, it results in a robust, cohesive gel with enhanced durability and lift capacity. This formulation is specifically designed for the correction of deep wrinkles, pronounced folds, and restoration of significant facial volume.

REVANESSE® Ultra+ Lidocaine typically contains 25mg/mL of cross-linked HA and is formulated with 0.3% lidocaine hydrochloride to enhance patient comfort during injection. It is indicated for injection into the deep dermis or subcutaneous tissue to treat areas such as deep nasolabial folds, marionette lines, and for facial contouring or volume restoration (e.g., cheeks, chin).

Storage: REVANESSE® Ultra+ Lidocaine should be stored between 2°C and 25°C (36°F and 77°F). Do not freeze. Protect from light.

Authenticity: Health Supplies Plus guarantees that all REVANESSE® products are authentic, sourced through appropriate channels, and handled according to manufacturer specifications.

Note: For professional use only.

How does REVANESSE® Ultra+ Lidocaine work?

REVANESSE® Ultra+ Lidocaine addresses facial aging signs like deep folds and volume loss by providing immediate physical volume and structural support upon injection. Its high viscosity and cohesive properties, derived from the Thixofix® technology, make it particularly suitable for lifting and correcting deeper wrinkles and folds, such as prominent nasolabial folds, oral commissures, and marionette lines.

When injected into the appropriate tissue plane (deep dermis or subcutaneous tissue), the HA gel integrates and provides support, smoothing the appearance of deep facial lines and restoring lost volume in areas like the cheeks or temples. The hydrophilic nature of HA also helps attract and retain moisture within the tissue.

The results are typically visible immediately post-treatment, though optimal results are seen after initial swelling resolves. The duration of effect for REVANESSE® Ultra+ Lidocaine generally ranges from 9 to 12 months, but this can vary based on patient metabolism, lifestyle, injection area, and volume used. The inclusion of lidocaine helps mitigate discomfort during the procedure, which typically takes 30-60 minutes.

Indications for Use

REVANESSE® Ultra+ Lidocaine is indicated for adults (typically 21 years and older, consult local regulations/IFU) seeking correction of deep facial wrinkles, pronounced folds, and significant volume loss. Specific uses include:

• Correction of deep nasolabial folds.
• Treatment of pronounced marionette lines and oral commissures.
• Restoration of volume in areas such as the cheeks, temples, or chin.
• Facial contouring requiring a filler with higher viscosity and lift capacity.

Appropriate patient selection depends on a thorough assessment of facial structure, skin quality, patient goals, and consideration of contraindications as outlined in the product’s Instructions for Use (IFU).

Primary Benefits

• High viscosity formulation provides significant lift and volume restoration.
• Specifically designed for correcting deep wrinkles and pronounced facial folds.
• Utilizes Thixofix® cross-linking for a durable, cohesive gel.
• Provides immediate, visible results for volume and contouring.
• Contains lidocaine for improved patient comfort during injection.

Side Effects and Safety Information

Practitioners must consult the complete Instructions for Use (IFU) provided with the product for comprehensive information on indications, contraindications, warnings, precautions, and potential adverse events. It is essential to discuss all potential risks and side effects with patients prior to treatment.

Common side effects are typically mild to moderate, temporary, and related to the injection site, including:

• Swelling
• Bruising
• Redness
• Tenderness or Pain
• Itching
• Firmness or Lumps/Bumps at the injection site

Severe Adverse Events:
As with any dermal filler injection, there are risks of more serious complications. Practitioners must possess thorough anatomical knowledge, use appropriate injection techniques, and be prepared to manage complications. Potential severe adverse events include:

• Vascular Occlusion (VO): Accidental injection into a blood vessel can obstruct blood flow, potentially leading to tissue necrosis (tissue death), scarring, or (in rare cases involving facial arteries) blindness or stroke. Prompt recognition and management according to established protocols are crucial, especially when injecting in high-risk areas.
• Severe allergic reactions (anaphylaxis)
• Inflammation, infection, or abscess formation
• Granuloma or persistent nodule formation
• Migration of filler
• Prolonged pain or numbness
• Herpetic eruptions (cold sores) in susceptible individuals