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Revolax Sub-Q Lidocaine

$29.50

Revolax Sub-Q Lidocaine​​ is a KFDA-certified monophasic dermal filler containing 24 mg/mL high-purity hyaluronic acid (98.7% purity) and 0.3% lidocaine. Engineered with triple cross-linking technology, it delivers 8-12 month longevity for facial contouring and wrinkle correction while reducing injection pain by 78% – clinically proven 93% patient satisfaction in volume restoration.

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Description

Revolax Sub-Q Lidocaine Dermal Filler

Premium Monophasic HA Filler with Integrated Anesthetic

Medical Grade Formulation

KFDA-certified dermal filler containing 24 mg/mL high-purity hyaluronic acid with integrated 0.3% lidocaine. Features optimized 3D molecular structure providing 1.2 million mPa·s viscosity for structural support. Clinically proven 93% patient satisfaction in volume restoration with 8-12 month persistence. Reduces injection pain by 78% compared to non-anesthetic formulas.

Clinical Advantages

Pain Reduction

Integrated 0.3% lidocaine reduces discomfort by 78% during administration

High Purity

98.7% non-animal stabilized HA with ultra-low endotoxins (<0.05 EU/mg)

Structural Support

1.2 million mPa·s viscosity for optimal volume in deep tissue

Longevity

8-12 month duration through advanced cross-linking technology

Advanced Technology

Molecular Optimization

  • Monophasic gel structure
  • Triple cross-linking technology
  • Optimized 3D molecular configuration

Performance Metrics

  • Viscosity: 1,200,000 mPa·s
  • G prime: Optimal for deep support
  • Swelling rate: <2% reported cases

Packaging Specifications

Storage: 2-25°C in original packaging

Shelf Life: 24 months from manufacture

Do Not: Freeze or expose to sunlight

Disposal: Single-use only

Clinical Protocol

Injection Parameters

  • Needle: 25G-27G cannula
  • Depth: SubQ/Supraperiosteal
  • Max per session: 2.0mL

Indications

  • Facial contouring
  • Deep wrinkle correction
  • Lip augmentation

Post-Care

  • Cold compress application
  • No pressure for 72hrs
  • Follow-up at 2-4 weeks

Contraindications

Avoid in pregnancy, active inflammation, hypersensitivity to gram-positive bacteria, bleeding disorders, or active skin infections.

Medical Use Only

* Individual results may vary based on metabolic factors and injection technique. This product is for licensed practitioners only. Manufactured by Across Co. Ltd. (GMP 4103), Busan, South Korea. Certifications: KFDA 15-542, CE 0481, ISO 13485:2016. Report adverse events to local health authorities. Our company bears no responsibility for off-label use.

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