JUVEDERM® VOLIFT RETOUCH w/ Lidocaine

Where can I buy this product?

JUVEDERM® VOLIFT RETOUCH w/ 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 JUVEDERM® VOLIFT RETOUCH w/ Lidocaine?

JUVEDERM® VOLIFT RETOUCH w/ Lidocaine is a sterile, pyrogen-free, physiological solution of cross-linked hyaluronic acid (HA) gel utilizing Allergan’s advanced Vycross® technology. It contains the same formulation as Juvéderm® Volift but is provided in **smaller volume syringes (typically 2 x 0.55ml)**, making it ideal for touch-up sessions, refining previous treatments, or addressing smaller areas requiring correction.

This formulation typically contains 17.5mg/mL of hyaluronic acid and includes 0.3% lidocaine hydrochloride to enhance patient comfort. It is indicated for injection into the deep dermis for the treatment of medium to deep facial lines, wrinkles, and folds (such as nasolabial folds) and for restoring facial contours.

Storage: JUVEDERM® VOLIFT RETOUCH w/ 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 JUVEDERM® products are authentic, sourced through appropriate channels, and handled according to manufacturer specifications.

Note: For professional use only.

How does JUVEDERM® VOLIFT RETOUCH w/ Lidocaine work?

JUVEDERM® VOLIFT RETOUCH w/ Lidocaine employs Allergan’s Vycross® technology, which optimizes HA cross-linking for a smooth, efficient, and durable gel. When injected into the deep dermis, it restores volume to smooth medium to deep facial lines and folds, providing natural-looking results with good tissue integration.

The “Retouch” format allows practitioners precise control for follow-up treatments to maintain optimal correction, or for treating smaller anatomical areas or finer adjustments where a full 1ml syringe might be excessive. The Vycross® technology contributes to the gel’s longevity and smooth feel.

Results are visible immediately, with the Vycross® formulation known for potentially causing less swelling than other technologies. The duration of effect for the Volift formulation is clinically shown to last up to 15 months, although individual results vary. The integrated lidocaine minimizes discomfort during the procedure.

Indications for Use

JUVEDERM® VOLIFT RETOUCH w/ Lidocaine is indicated for adults (typically 21 years and older, consult local regulations/IFU) for:

• Touch-up or follow-up treatments to maintain correction previously achieved with Juvéderm® Volift or similar fillers.
• Correction of medium to deep facial wrinkles and folds (e.g., nasolabial folds) requiring smaller volumes.
• Fine-tuning facial contours or addressing smaller areas of volume loss.
• Use in areas where precise, smaller volume injections are preferred.

Appropriate patient selection and injection technique, considering the specific volume needed, are essential. Practitioners should consult the Instructions for Use (IFU) for full details.

Primary Benefits

• Provides the effective Volift formulation (Vycross® technology) in a smaller volume (0.55ml) for precise touch-ups or smaller corrections.
• Effectively treats medium to deep facial lines and folds.
• Smooth gel integrates well for natural-looking results.
• Offers results lasting up to 15 months (characteristic of the Volift formulation).
• Contains lidocaine for improved patient comfort during injection.
• Reduces potential product waste when only small volumes are needed.

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. Proper injection technique is critical for safety and optimal results.

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 (usually temporary)
• Indurations or nodules

Severe Adverse Events:
As with any dermal filler injection, there are risks of more serious complications. Practitioners must possess thorough anatomical knowledge 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 are critical.
• 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
• Hypersensitivity reactions