Biotechnological Performance Metrics
• Transepidermal Water Loss (TEWL): Reduced by 28% within 72 hours of initial application.
• Fibroblast Activation: Exosomal signaling increases metabolic activity in dermal fibroblasts by 300%.
• DNA Repair: PDRN fragments (Salmon DNA) provide nitrogenous bases for rapid tissue regeneration.
• Elasticity Index: Significant improvement of 45% recorded over a 3-week clinical cycle.
CMK Laboratory Certified
Study ID: CMK-2023-HAX
Sample Size: 150 Participants
Duration: 8-Week Longitudinal Study
Application Protocol for Clinical Professionals
Phase: Preparation
Decontaminate skin using a non-abrasive pH-balanced tonic. Ensure the dermal barrier is receptive but not compromised.
Phase: Administration
Apply the 2.5ml ampoule in its entirety. Optimal delivery via topical absorption on damp skin or professional MTS (Microneedle Therapy System).
Phase: Maintenance
Maintain 3-5 week intervals between cycles. Store unsealed units in a climate-controlled environment below 15°C.
Professional Safety Standards
Contraindicated for patients presenting with active rosacea, impetigo, or localized viral infections. Post-procedure erythema is expected to resolve within 2-4 hours.
“Clinical data suggests a cumulative efficacy profile. Maximum tissue density is typically achieved following the 3rd consecutive treatment cycle.”
Ingredients Transparency (E-E-A-T Compliance)
• Medical-Grade Sodium Hyaluronate
• Hydrolyzed Salmon DNA (PDRN 98.3%)
• Centella Asiatica Derived Exosomes
• Biomimetic Peptide Complex (sh-Oligopeptide-1)
© 2026 FILLERS FAIRY | CLINICAL DERMATOLOGY DIVISION

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