Price range: $360.99 through $922.99
Description
DYSPORT® is an abobotulinumtoxinA injectable supplied as a sterile, lyophilized vial for intramuscular use in aesthetic and neurological care. Clinics stock this preparation to standardize neuromodulator workflows across indications, with US distribution supporting dependable replenishment. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
What Dysport Is and How It Works
This botulinum toxin type A neuromodulator supports chemodenervation protocols used by dermatology, plastic surgery, and neurology teams. Dysport injectable is reconstituted with sterile saline and administered by licensed professionals via intramuscular injection. In practice, it temporarily reduces local muscle activity through inhibition of acetylcholine release at the neuromuscular junction.
The formulation’s accessory protein profile may support a controlled diffusion pattern across broader treatment fields when applied by experienced injectors. Technique, anatomy, and reconstitution approach guide outcomes. This class has a long history in both aesthetic line management and functional muscle tone programs.
For additional agents within this class, see Botulinum Toxins.
Professional Applications
Clinics use this preparation in established neuromodulator workflows across aesthetic and therapeutic settings. Common aesthetic applications include upper-face line softening within on-label protocols and informed off-label practice patterns where appropriate. Many teams also integrate it into multidisciplinary programs focused on muscle tone modulation for select neurologic indications under licensed supervision.
Typical cosmetic focus areas include forehead and periorbital regions. Practices also employ Dysport for glabellar lines when refining dynamic expressions through carefully planned treatment maps. In therapeutic settings, trained specialists integrate the product into individualized regimens, coordinating evaluation, dosing strategy, and follow-up within clinic policy.
For technique overviews and consultation planning tips, review Dysport Injections.
Key Features
- Botulinum toxin type A: AbobotulinumtoxinA in a sterile, lyophilized form.
- Single-use format: Individually sealed vial intended for one patient session.
- Flexible protocols: Supports aesthetic and neurological practice needs.
- Reconstitution guidance: Use sterile saline per manufacturer instructions.
- Clear labeling: Lot number and expiry readily visible on the outer carton and vial.
- Team efficiency: Consistent presentation helps standardize clinic workflows.
- Quality packaging: Tamper-evident closure and protective secondary packaging.
- Dysport vials: Designed for precise handling by trained staff.
- Storage reference: See our Storage Guide for general neurotoxin considerations.
Benefits in Practice
This product fits well into busy schedules, allowing providers to map efficient injection plans and stagger follow-ups. Teams can align assessment, preparation, and administration steps around a predictable vial presentation, which helps streamline room turnover and supply checks.
The formulation’s diffusion profile can support coverage of larger functional units with thoughtfully placed injection points. Providers often value the balance between targeted action and natural-looking outcomes when treatments are planned around patient-specific anatomy and muscle dynamics.
Inventory planners benefit from consistent packaging, clear batch details, and straightforward intake checks. These factors make cycle counting and expiry rotation simpler across multi-provider practices.
Protocol standardization is another advantage. Whether a clinic focuses on upper-face aesthetics or functional tone programs, consistent vial handling and labeling help maintain continuity between providers. Teams can align teaching files, staff training, and post-visit documentation to reduce variability and support quality assurance.
Where a clinic prefers to maintain a unified neuromodulator line across locations, having a single reference product can simplify formulary decisions and malpractice documentation. The flexibility to accommodate different clinical programs under one neuromodulator class also streamlines patient education materials and follow-up checklists.
For comparative context in practice planning, see Xeomin vs Dysport.
Inventory choices can also reflect dosing protocols in specialty services. Some programs prefer to stage smaller or larger single-use vials to match typical session volumes and reduce waste. When rolling out training, consistent device handling and setup checklists save minutes per room, which adds up across a full session day.
Clinics that serve multidisciplinary patient populations often appreciate having a standardized option compatible with both aesthetic and medically oriented schedules. This helps maintain predictable lead times for supplies and supports predictable clinic capacity planning.
For teams that document product lineage across treatment notes, uniform carton and vial identifiers help with traceability and reconciliation during periodic audits of clinical supplies.
Composition & Ingredients
Active component:
- AbobotulinumtoxinA
Other components are provided as listed on the manufacturer’s label and package insert. Refer to the specific pack in hand for a complete, current composition summary.
Packaging & Supply
This preparation is supplied as a sterile, lyophilized powder in a single-use vial. Vial content is reconstituted with sterile saline according to the manufacturer’s instructions for intended intramuscular administration by licensed professionals.
Available presentations include Dysport 500 Units for higher-dosage clinical protocols, as well as a smaller 300-unit vial commonly used in aesthetic programs. Each vial and carton displays lot and expiry for straightforward intake and inventory rotation. Packaging includes tamper-evident features to support chain-of-custody practices in the clinic.
Important use notes:
- For professional use only; prescription product.
- Reconstitute and administer only per the manufacturer’s guidelines.
- Use in accordance with local regulations and clinic policy.
To review related items within this brand family, visit Dysport Brand.
Ordering & Logistics
Your account must be verified before ordering. Sign in to view specifications, available presentations, and pricing tiers aligned to clinic volume. Contract and bulk arrangements are available for qualified facilities. Orders are processed through vetted distribution channels and shipped using reliable carriers with standard tracking.
For adjacent categories that support your injection workflows, explore Pharmaceuticals.
Comparable Products
Clinics that evaluate alternative type A neuromodulators often compare this preparation with established brands. Explore Xeomin for a purified formulation option, or review Botox as another well-known reference standard in this class.
Pricing & Access
Sign in to see current pricing. Volume and contract tiers are available for eligible clinics, group practices, and networks. Your account manager can assist with multi-site coordination and periodic review based on utilization patterns.
Availability & Substitutions
Supply can vary by presentation and seasonality. If your preferred vial size is temporarily limited, our team can suggest clinically appropriate substitutes in the same class after confirming your protocol needs. We recommend aligning substitutions with your formulary and documentation standards before scheduling patients.
Authoritative Sources
Sign in to order for licensed use; we provide temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
How does this neurotoxin compare with other type A preparations?
This product belongs to the botulinum toxin type A class used for localized chemodenervation. Compared with several alternatives, it features a well-established safety and handling profile when used by trained professionals. Some clinicians note a diffusion pattern that can suit broader fields, depending on technique and anatomy. Selecting between Dysport, Xeomin, or Botox typically depends on training background, desired handling characteristics, and program goals rather than a single superiority metric.
How should vials be received and stored in the clinic?
On receipt, inspect outer cartons for integrity, then confirm lot and expiry against your purchase record. Store according to the manufacturer’s label and your clinic policy. Maintain segregation of quarantined stock until intake checks are complete. Keep reconstitution supplies and sharps disposal available where you stage neuromodulation procedures. Follow the package insert for storage limits before and after reconstitution, and document inventory movements for traceability.
Which vial size fits aesthetic sessions versus larger programs?
Many aesthetic sessions use smaller single-use vials to limit waste, while larger multidisciplinary programs often stage higher-unit vials to accommodate broader treatment maps. Your choice should align with procedure mix, injector preference, and scheduling needs. Consider standardizing to a primary vial size for inventory simplicity, and keep a small reserve of the alternate size for edge cases or high-volume clinic days. Always follow labeling and clinic policy.
What training is recommended for safe administration?
Administration should be limited to licensed medical professionals trained in facial anatomy or relevant neuromuscular anatomy, sterile technique, and complication management. Many clinics pair didactic education with supervised hands-on sessions before independent practice. Periodic skills refreshers help align technique across teams and reduce variability. Keep emergency protocols and adverse event reporting processes accessible in every procedure room.
How does diffusion influence injection planning and follow-up?
Diffusion can vary with injection depth, dilution, anatomy, and muscle mass. Plan injection points to match functional units rather than single lines when appropriate. Document the map and volume used per site to simplify future adjustments. Schedule follow-up visits to assess symmetry and patient-specific response. A consistent charting template allows comparisons over time and helps different providers align touch-up decisions.
What labeling information is most useful for documentation?
Clinics usually record brand, lot number, expiry date, vial size, and reconstitution details. Labeling on the carton and vial typically provides lot and expiry, which supports traceability. Retain the vial or label tab in the chart when feasible. Standardize where you record these data in your EHR or paper chart to make audits faster and ensure continuity when multiple injectors share a patient’s care plan.
How can clinics integrate this product into existing consent and workflow steps?
Start by aligning your consent form to reflect neuromodulator class risks and benefits, and confirm the target areas documented for each session. Build a checklist that covers intake, reconstitution, labeling, timeout, and post-injection instructions. Train team members on room setup, sharps safety, and spill procedures. Finally, monitor procedure times and adjust scheduling templates to match real-world turnover, keeping buffer slots for follow-ups and new consultations.
Specifications
- Main Ingredient: Botulinum Toxin Type A
- Manufacturer: Galderma
- Drug Class: Dermal Filler
- Generic Name: Botulinum Toxin Type A
- Package Contents: 1 Vial | 2 Vials
- Storage Requirements: Refrigerated between 2°C – 8°C
- Main Usage:
About the Brand
Dysport
Here to help
Questions about ordering, delivery or products? You can email our team here or call now at 1-800-630-9757 and be connected with your dedicated Account Manager
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