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Product information
| Active substances | CROSS LINKED HYALURONIC ACID, LIDOCAINE |
|---|---|
| Manufacturer | Across Co. |
| Pack size | 1 x 1.1 ml Pre-Filled Syringe, 2 x 25G Needles |
| Strength | 24mg/ml HA, 0.3% Lidocaine |
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Revolax Sub-Q with Lidocaine is a premium dermal filler for facial contouring and deep wrinkle treatment. The product combines a high concentration of hyaluronic acid (24 mg/ml) with 0.3% lidocaine, allowing for comfortable treatment while delivering effective results. The filler’s thick, dense consistency makes it great for treating deep to severe wrinkles and enhancing facial features such as the cheeks, chin, nose, and jawline.
The filler’s hyaluronic acid is derived from Streptococcus zooepidemicus bacterial fermentation and undergoes thorough purification to ensure minimal bacterial toxins. Through BDDE cross-linking, the gel achieves a consistent texture that provides both durability and natural-looking results, typically lasting between 12 to 18 months.
The dermal filler‘s formulation allows medical professionals to easily mold and shape the product during treatment while maintaining structural integrity once injected. This makes it an effective REVOLAX product solution for medical practitioners who need to achieve significant volumizing results or perform detailed facial contouring while ensuring patient comfort throughout the procedure.
This dermal filler is primarily used for treating deep to severe facial wrinkles and significant facial contouring. Specific applications include:
Revolax Sub-Q with Lidocaine is manufactured by Across, a South Korean company specializing in aesthetic medicine. The production process involves the bacterial fermentation of Streptococcus zooepidemicus to create hyaluronic acid. The acid undergoes thorough purification to minimize bacterial endotoxins. The gel is then cross-linked using BDDE to achieve its specific consistency and properties.
Main components include:
Device properties:
Each package contains:
The treatment must be performed by qualified medical professionals following these steps:
Patients should follow these recommendations:
Results typically last between 12 and 18 months. For optimal results, patients should schedule maintenance treatments before the effects fully diminish.
Common side effects include:
These reactions typically resolve within two weeks. Patients should seek medical attention if symptoms persist or worsen.
The treatment is not suitable for: