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DIVA FACE PN 40mg*2ml

$49.00

LEXYAL DIVA FACE PN 40mg*2ml is a professional-grade skin rejuvenation treatment utilizing medical-grade Polynucleotides derived from Salmon DNA. Clinically proven to reduce dead skin cells by 27% and increase moisture by 35%, this advanced formula stimulates fibroblast migration by 68% for enhanced collagen production, effectively reducing wrinkles and improving skin firmness. Ideal for those seeking non-surgical facial rejuvenation.

Quantity discounts
Quantity Discount Price
5-9 3% $47.53
10-19 5% $46.55
20-Unlimited 8% $45.08
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LEXYAL DIVA FACE PN 40mg/2ml

Medical Compliance: | | Clinical Reference: Sci Rep 2020;10:1-12

Clinical Efficacy & Data


Hydration Metrics

Corneometer evaluations indicate a 35% increase in stratum corneum hydration. Sustained moisture retention observed 16 weeks post-treatment.

Fibroblast Migration

In-vitro testing demonstrates a 68% enhancement in fibroblast migration velocity, accelerating tissue repair and endogenous collagen synthesis.

Cellular Exfoliation

Quantitative analysis shows up to a 27% reduction in dead skin cell accumulation, regulating keratinization processes safely.

Formulation Specifications


Active Component: 40mg highly purified Polynucleotides (PN) extracted from Salmon DNA fragments via advanced bio-engineering.

Packaging Volume: 2.0ml pre-filled, sterile medical (1 unit per package).

Safety Profile: Endotoxin levels strictly maintained at < 0.05 EU/g. Optimal physiological pH (6.8 – 7.5).

Viscosity: Medium viscosity optimized for uniform dermal distribution and sustained absorption.

Clinical Administration Protocol


Injection Technique: Micro-papule or mesotherapy injection grid.

Target Depth: Dermal layer (1.5mm – 2.0mm depth).

Recommended Gauge: 30G or 32G.

Dosage per Point: 0.05ml, spaced 1.0cm apart.

Treatment Cycle: Standard protocol requires 3-4 consecutive sessions executed at 2-4 week intervals.

Medical Disclaimer

Strictly designated for professional cosmetic administration by licensed medical practitioners. Contraindicated for patients presenting active dermatological infections, auto-immune pathology, pregnancy, or lactation. Efficacy timelines are patient-dependent; baseline histological improvements mandate minimum 16-week post-treatment evaluation.

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