Lipo Lab V-Line Premium: Submental & Facial Contouring Ampoules
Clinically Assessed Efficacy Data
Phase II Target Subject (n=124)
Formulated for localized adipocyte volume reduction and concurrent dermis laxity management. Incorporates 98% high-purity L-Carnitine acting synergistically with proprietary lipolytic compounds. Excludes Phosphatidylcholine (PPC) to mitigate risks of severe localized necrosis and prolonged recovery metrics.
Active Compound Matrix
L-Carnitine (98%): Accelerates mitochondrial fatty acid oxidation parameters.
Juglans Regia Extract: Botanical alpha-linolenic acid source; enhances localized lymphatic clearance.
Aesculus Hippocastanum: Modulates capillary permeability to suppress post-procedure edema incidence.
Clinical Efficacy Metrics
Response Rate: 81.5% documented >2mm submental volume reduction at Week 4 interval.
Effect Duration: Median visible contour maintenance of 38 weeks post-cycle.
Adverse Events: Transient edema (14%), mild erythema (8%). 100% resolution within 72 hours.
Strict Administration Protocol
Dosage Parameters
0.15cc to 0.20cc per injection site. Absolute maximum of 2.0cc per session for facial zones.
Depth & Spacing
Target depth: 5.0mm (subcutaneous fat layer). Maintain strict 1.0cm to 1.5cm grid spacing.
Cycle Frequency
Recommended 3 to 5 continuous sessions. Mandatory 10 to 14-day resting interval between sessions.
Packaging: 10ml × 5 sterile
Formulation: RTU (Ready-to-Use) Liquid
Storage parameters: 2°C – 25°C
Shelf Life: 36 months
RESTRICTED MEDICAL ARTICLE & CONTRAINDICATIONS: Distribution and application strictly restricted to licensed medical practitioners. Unapproved for intravenous (IV) or intramuscular (IM) administration. Absolutely contraindicated for pregnant or lactating women, patients with active thyroid dysfunctions, microangiopathy, or known hypersensitivity to Juglans Regia (nut allergen cross-reactivity). Clinical efficacy metrics are derived from manufacturer internal phase trials; product is not evaluated by the. Practitioner must evaluate individual patient biochemistry prior to application.

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