Price range: $346.99 through $389.99
Description
Xeomin® is a botulinum toxin type A supplied as a lyophilized powder for solution intended for intramuscular injection. Clinics use this purified incobotulinumtoxinA in aesthetic and therapeutic programs that require precise, localized muscle relaxation. Facilities stock it for predictable performance, clear labeling, and dependable supply supported by US distribution.
What Xeomin Is and How It Works
This preparation contains incobotulinumtoxinA, a type A neurotoxin produced by Clostridium botulinum. After reconstitution with sterile 0.9% sodium chloride, it is administered intramuscularly by trained professionals. The product is free of accessory complexing proteins, which supports a focused formulation for procedural planning. Typical protocols favor its consistent onset and duration observed in routine practice.
Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors. The line is widely incorporated by dermatology, plastic surgery, and neurology teams for structured injection workflows. For catalog breadth within botulinum toxins, see Botulinum Toxins or review market context in Top Botulinum Toxins.
Professional Applications
Clinics deploy this product across aesthetic schedules for glabellar lines, forehead lines, and periocular areas, as permitted by local scope and prescriber direction. Therapeutic service lines may also include neurotoxin procedures within specialty clinics. Treatment mapping, dilution approaches, and intervals follow the manufacturer’s labeling and internal protocols. When planning product schedules and budgets, Xeomin cost is considered alongside staffing, chair time, and documentation needs. For cross-brand context, see our Comparative Review.
Key Features
- Purified active toxin: incobotulinumtoxinA
- No complexing proteins: streamlined composition
- Lyophilized sterile powder: reconstituted before use
- Intramuscular route: procedural control for targeted muscles
- Consistent labeling: lot and expiry visible
- Unit-of-use vials: single-patient application per vial
- Reconstitution: 0.9% sterile saline per labeling
- Procurement confidence: sourced via vetted distributors
Benefits in Practice
Teams value predictable preparation steps that fit short appointment blocks. The product integrates cleanly with standard injection setups, minimizing room turnover time. Consistency supports repeatable mapping patterns and straightforward training for new injectors under supervision. Label clarity aids EHR capture of lot and expiry, supporting quality systems and recall readiness.
Budgeting and forecasting improve when product usage, session counts, and consumables are standardized. Many clinics model Xeomin injections cost within broader service-line KPIs. Clear vial identification helps avoid selection errors during high-volume days. For placement planning by facial area, see the quick reference on Injection Sites.
Composition & Ingredients
Active ingredient: incobotulinumtoxinA (botulinum toxin type A). Excipients typically include human albumin and sucrose. The toxin is presented as a sterile, preservative-free, lyophilized powder for solution, intended for intramuscular administration following reconstitution. Certain presentations provide IncobotulinumtoxinA 50 Units per vial as one of the available options. Clinics should prepare and handle vials according to the manufacturer’s instructions and institutional policies.
Packaging & Supply
Vials arrive as sterile, single-use, lyophilized powder requiring reconstitution with sterile saline prior to injection. Labels display product identity, lot number, and expiration date to support inventory control. Many clinics standardize on clearly marked trays for setup and segregation by toxin type. A commonly used pack is the Xeomin 100 Units vial for higher-throughput schedules; an alternate vial strength is also available to suit varied protocols. Store and handle per labeling and your facility’s SOPs.
Ordering & Logistics
Licensed account verification is required to view and purchase. Sign in to access volume and contract tiers aligned to your organization. You may submit purchase orders or use approved payment methods after account approval. If your team evaluates cost models across toxins, IncobotulinumtoxinA price per unit can be compared within your formulary framework. For related therapeutics and injectables, browse Pharmaceuticals. Product handling and transit follow applicable regulations and carrier practices.
Comparable Products
Clinics often benchmark this preparation alongside other botulinum toxin type A brands. Consider Dysport for comparative planning, or evaluate Botox when assessing formulation preferences, spread characteristics, and scheduling considerations. Selection should reflect prescriber experience, patient profile, and operational fit within your service lines.
Pricing & Access
Sign in to view wholesale options, negotiated tiers, and available packs. Facilities can align purchases with forecasted utilization and appointment cadence. Many purchasing teams track Xeomin price per unit to support margin planning across aesthetic and therapeutic programs. Contract terms, order frequency, and fulfillment timing may influence unit economics. Contact your internal procurement lead for approved buying paths and formulary controls.
Availability & Substitutions
Supply may vary by manufacturer output, seasonal demand, and allocation priorities. If a specific presentation is temporarily constrained, your team may confirm acceptable substitutions within the same class based on clinical protocol, labeling, and prescriber guidance. We recommend validating any substitutions with the treating provider and updating inventory systems accordingly. No restock timelines are guaranteed; check current availability when scheduling.
Authoritative Sources
Sign in to verify licensed access and request vials with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
What sets this neurotoxin apart for clinical use?
It contains incobotulinumtoxinA in a purified, accessory protein–free formulation. Many teams appreciate the consistent reconstitution process, predictable workflow fit, and clear vial labeling for lot and expiry capture. These attributes support scheduling efficiency, training, and inventory control. Selection should ultimately reflect prescriber experience, patient profiles, and your clinic’s formulary guidance across botulinum toxin options.
How is it typically incorporated into aesthetic or neuro procedures?
Clinics implement structured mapping and dilution protocols under prescriber oversight. It is used in aesthetic sessions and in specialty clinics for neuro-focused indications, following labeling and local regulations. Most facilities align room setup, documentation, and follow-up intervals to their internal SOPs. Product choice is often informed by injector familiarity, desired handling characteristics, and overall program design.
What handling considerations apply before and after reconstitution?
Use sterile technique and reconstitute with 0.9% sodium chloride per the manufacturer’s instructions. Prepare only the amount needed for the session and adhere to single-use vial practices. Follow storage and in-use time guidance on the label and your facility’s policies. Maintain chain-of-custody documentation and record lot and expiration details in the patient record according to your quality procedures.
How long do effects generally persist between visits?
Duration varies by indication, dose, and injection pattern. In routine practice, many providers observe intervals often around three to four months for aesthetic schedules, with adjustments made per response and labeling. Actual timing should be individualized by the prescriber based on goals, tolerability, and prior response, and not all patients will follow the same interval.
Can it be coordinated with fillers or threads in the same plan?
Combined treatment plans are common in aesthetic practice. Sequencing and intervals depend on the anatomical goals, product classes involved, and clinician preference. Many teams schedule neurotoxin sessions first, then reassess tissue balance for adjunctive procedures. Final decisions should reflect labeling, professional standards, and your clinic’s protocol hierarchy for multi-modality care.
What vial configurations are available to clinics?
Multiple strengths are offered to accommodate different program needs. Each vial is a sterile, lyophilized powder for solution intended for intramuscular administration after reconstitution. Your purchasing team can confirm current presentations in the portal and select the option that aligns with the planned mapping and volume per session for your service mix.
What is required to order through the portal?
Access is limited to licensed healthcare entities. Account verification typically includes clinic credentials and prescriber information as applicable. After approval, authorized users can view packs, contract tiers, and submit purchase orders. Pricing visibility and fulfillment options reflect your account status and negotiated terms. Always align ordering with your facility’s procurement policies and formulary controls.
Specifications
- Main Ingredient: Botulinum Toxin Type A
- Manufacturer: Merz Pharmaceuticals
- Drug Class:
- Generic Name: Incobotulinumtoxina Injections
- Package Contents: 100 U x 1 Vial
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage:
About the Brand
Xeomin
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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