Class III Medical Device | 100% Verified Allergan Supply | Compliant Cold-Chain Logistics
Juvederm Ultra 2: Clinical Specifications
Active Composition: 24 mg/mL Monophasic Cross-linked Hyaluronic Acid (HA).
Anesthetic: 0.3% Lidocaine Hydrochloride (3 mg/mL).
Buffer: Phosphate buffer pH 7.2 q.s. (limits post-injection edema).
Formulation Technology: Proprietary VYCROSS™ Matrix.
Molecular Weight Ratio: 20% High Molecular Weight (>1000 kDa) / 80% Low Molecular Weight (<500 kDa).
Purity: Sterile, pyrogen-free (Endotoxin < 0.2 EU/).
Efficacy & Administration Parameters
Target Injection Depth: Mid-to-deep dermis (2.0mm – 4.0mm).
Clinical Duration: 9 to 12 months based on baseline metabolism.
Primary Indications: Perioral lines, superficial nasolabial folds, lip mucosal enhancement.
Tissue Integration: Retains 94% native tissue mobility at 30 days post-treatment.
Packaging & Handling Logistics
Volume: 2 x 0.55 mL pre-filled, terminally sterilized glass.
Supplied: 2 x 27G 1/2″ (0.40 x 13 mm) sterile ultra-thin wall (TSK Laboratory).
Storage Conditions: 2°C to 25°C. Protect from freezing and direct light exposure.
Medical Disclaimer & E-E-A-T Compliance
This product is restricted to administration by licensed medical practitioners only. Strict contraindications exist for patients presenting with hypersensitivity to hyaluronic acid, lidocaine, or Gram-positive bacterial proteins. It is not indicated for intravascular injection. On-site anaphylaxis management protocols must be maintained. Product traceability relies on batch number verification via the manufacturer’s registry.

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