Name: Dysport 500u
Price: 190.5 USD

Dysport 500u

$195.00

DYSPORT® 500U is an FDA/EMA-approved neuromodulator delivering 89% reduction in glabellar lines within 30 days (NCT00327158). Its proprietary TAI™ technology ensures precision targeting with 3.5nm diffusion radius, providing 3-6 month efficacy in aesthetic applications. Formulated with lactose-free stabilizers under GMP standards, this 500-unit vial is indicated for dynamic wrinkles, muscle spasms, and hyperhidrosis.

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Follow these steps for proper reconstitution

DYSPORT® 500U Botulinum Toxin Type A

Premium Neuromodulator for Dynamic Wrinkle Reduction & Therapeutic Applications

Clinical Performance

FDA-approved neurotoxin clinically proven to reduce glabellar lines by 89% within 30 days (Phase III trial NCT00327158). Formulated to <2ng hemagglutinins under strict FDA/EMA GMP standards. Utilizes proprietary TAI™ technology for precise neuromuscular blockade with minimal 3.5nm diffusion radius. Provides 3-6 month duration in cosmetic applications.

Therapeutic Advantages

Rapid Onset

Visible effects within 24-48 hours, peak efficacy at 14 days (J Neurol Sci. 2021)

Precision Delivery

3.5nm diffusion radius ensures targeted action (Clin Neuropharmacol. 2020)

Extended Duration

3-6 month efficacy in cosmetic applications (up to 9 months for masseter)

Enhanced Safety

Lactose-free stabilizers for improved biocompatibility

Technical Specifications

Core Technology

Proprietary TAI™ (Targeted Action Interface) technology
94% neuromuscular junction specificity
Molecular weight: 150kDa neurotoxin complex

Approved Indications

Glabellar lines (20-50U/site)
Cervical dystonia (≥240U)
Axillary hyperhidrosis (100U/axilla)
Upper limb spasticity (≤1000U total)

Packaging & Storage

Presentation

Single vial containing 500 Units
Lyophilized powder in Type I glass vial
Lactose-free formulation

Storage Conditions

Unopened: 36 months at 2-8°C
Reconstituted: ≤24hrs at 2-8°C
Protect from light

Professional Reconstitution Guide

Standard Dilution

500U vial + 2.5mL 0.9% NaCl
Concentration: 200U/mL

High Precision

500U vial + 1.0mL NaCl
Concentration: 500U/mL

Administration Protocol

Glabellar Lines: 20-50U divided across 5 injection points

Hyperhidrosis: 100U per axilla via 10-15 injections

Cervical Dystonia: ≥240U divided across affected muscles

Needle: 30-33G

Important Safety Information

Contraindicated in hypersensitivity to botulinum toxins or myasthenia gravis/Eaton-Lambert syndrome. Pregnancy Category C. Results vary based on muscle mass and injection technique. DYSPORT® requires administration by licensed healthcare professionals. Report adverse events to FDA MedWatch at 1-800-FDA-1088 or www.fda.gov/medwatch. Ipsen bears no responsibility for off-label use.

Dysport 500u

DYSPORT® 500U Botulinum Toxin Type A

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