REVANESSE® CONTOUR™ with Lidocaine

Description

Name:REVANESSE® CONTOUR™ with Lidocaine
Manufacturer: Prollenium Medical Technologies Inc
Active Substance(s): HYALURONIC ACID, LIDOCAINE
Strength: 25mg/ml HA, 3mg/ml Lidocaine
Pack Size: 1.2ML – 2 Pre-Filled Syringes
Package Content: 2 x 1.2ml Pre-Filled Syringes, 2 x 27G Needles

Revanesse® Contour™+ with Lidocaine is a high-density, cross-linked hyaluronic acid (HA) dermal filler designed for deep tissue facial volume restoration, particularly for the correction of moderate to severe facial wrinkles and lipoatrophy. Each syringe contains 25 mg/mL of HA and 0.3% lidocaine in a phosphate buffered saline solution, cross-linked with Butanediol Diglycidyl Ether (BDDE). The product is manufactured by Prollenium Medical Technologies Inc., ensuring pharmaceutical-grade quality and safety standards. The inclusion of lidocaine significantly reduces discomfort during injection, making procedures more tolerable for patients.

This injectable gel has a transparent, colorless, and odorless consistency and provides long-lasting results for up to 6–12 months, depending on the depth and site of administration. It is intended for intradermal use only, and should only be administered by qualified medical professionals trained in facial injection techniques. The product’s superior viscoelastic properties make it suitable for structural facial contouring and volume augmentation in key areas such as the cheeks and jawline.

• 25 mg/mL hyaluronic acid concentration for enhanced volumizing effect
• 0.3% lidocaine for increased patient comfort
• 6–12 month duration of results based on injection depth and site

Revanesse® Contour™+ with Lidocaine is supplied in sterile, pre-filled, disposable glass syringes. Each box includes two 1.2 mL syringes and up to two sterilized 27G needles, ensuring convenience and safety for clinical use. The packaging guarantees single-use integrity and prevents contamination.

The key ingredients of the product are:

• Cross-linked Hyaluronic Acid: 25 mg/mL
• Lidocaine Hydrochloride: 0.3% w/w
• Phosphate Buffered Saline: carrier solution
• Cross-linking agent: Butanediol Diglycidyl Ether (BDDE)

This product is indicated for the treatment of facial rhytides (wrinkles) and lipoatrophy by intradermal injection. It is particularly suited for deep dermal implantation, restoring lost facial volume and enhancing contour. The product maintains its effectiveness for an average of 6 to 12 months, depending on injection site and patient factors.

Contraindications include:

• Known allergy to lidocaine, hyaluronic acid, or BDDE
• Pregnant or breastfeeding women
• Use in eye contours (e.g., eyelids, tear trough)
• Patients with autoimmune disorders, severe allergies, or skin infections
• Children under 18 years
• Concurrent treatment with laser, chemical peels, or dermabrasion
• Injection into blood vessels, which may result in embolization
  

Possible side effects:

• Transient erythema, swelling, pain, itching, or tenderness
• Formation of nodules or induration at the injection site
• Rare cases of hypersensitivity (<1 in 1500 treatments)
• Reports of glabellar necrosis, granulomas, abscesses, and vision impairment if improperly injected

Revanesse® Contour™+ should only be administered by licensed professionals trained in soft tissue injection. The injection site must be thoroughly disinfected and the procedure carried out under sterile conditions. Before use, the syringe should be allowed to reach room temperature for 30 minutes.

Instructions for use:

• Inject slowly using the least amount of pressure required
• Always check for aspiration to avoid intravascular injection
• Discontinue immediately if blanching or unusual pain occurs
• Massage the area if blanching is observed to restore circulation
• Use product immediately after opening and do not reuse syringes or needles
  

Storage guidelines:

• Store between 2°C and 25°C
• Avoid freezing and protect from direct sunlight
• Do not use beyond the expiry date indicated on the box
  

This product is part of the Revanesse® range and should not be mixed with other dermal fillers or injected into areas previously treated with permanent fillers. Proper technique and patient screening are essential for optimal results and safety.

Warning! The product is intended solely for professional use in a medical environment and under professional supervision. The product is supplied to medical professionals who specialize in aesthetic medicine (plastic surgery, facial treatments) and work under individual medical licenses as aestheticians or in dedicated clinics. Unprofessional use by individuals without a medical background may lead to severe adverse effects and health harm.