Description
This botulinum toxin type A injectable vial is designed for licensed administration in clinical environments. Practices rely on this preparation for neuromodulator services across aesthetic and medical workflows. Your facility benefits from US distribution that supports predictable replenishment and planning.
What Nabota Is and How It Works
Nabota® is a botulinum toxin type A preparation supplied in a vial for injection by trained clinicians. It is used within professional protocols where temporary modulation of neuromuscular activity is required. At the cellular level, the toxin inhibits presynaptic acetylcholine release at the neuromuscular junction, which can reduce localized muscle activity for a defined duration when used as directed.
Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors. Our role is to help your team source established lines efficiently, with documentation and compatibility details that support your clinical workflows.
Clinicians typically integrate this class alongside assessment-driven mapping, aseptic technique, and post-procedure monitoring policies. For additional background on neurotoxins across brands and unit considerations, see Top Botulinum Toxin Injections and Exploring Botox Options.
Professional Applications
In practice, this neuromodulator supports common aesthetic protocols for the upper face under licensed supervision. Teams use it within standardized workflows that include facial mapping, dilution planning per labeling, and structured follow-up. It can also be incorporated into clinician-led programs that utilize neurotoxins for targeted neuromuscular modulation in medically supervised settings.
Facilities treat it as core inventory for scheduled clinic days and training sessions. As a result, Nabota 200U clinic supply may fit clinics seeking unit consistency and predictable handling characteristics. For category-level assortment and allocation planning, browse Botulinum Toxins or review the brand collection via our Brand Page.
Key Features
- Clinic-use vial: packaged for professional injection only
- Established class: botulinum toxin type A with standardized unit potency
- Consistent composition: human serum albumin and sodium chloride excipients
- Label clarity: lot number and expiry visible on the vial label
- Workflow fit: supports standard reconstitution practices per manufacturer guidance
- Quality standards: produced under controlled manufacturing and batch release oversight
- Single-vial format: aligns with appointment-based dosing plans
Benefits in Practice
This product supports efficient session planning and patient flow. A single vial format pairs well with templated mapping and documentation systems. Teams can align vial allocation to specific treatment rooms or providers, reducing handoffs and improving chain-of-custody clarity.
Consistent composition aids cross-coverage among staff trained on similar neurotoxin workflows. Labels with lot and expiry facilitate quick charting and inventory reconciliation. Many clinics also appreciate the simplicity of standard vial handling, which can streamline checks during setup, administration, and cleanup.
Composition & Ingredients
This Botulinum toxin type A 200 Units vial contains the active neurotoxin and established excipients. The formulation components are listed below for quick reference.
| Component | Amount | Role |
|---|---|---|
| Clostridium botulinum toxin type A | 200 Units | Active |
| Human serum albumin | 0.5 mg | Stabilizer |
| Sodium chloride | 0.9 mg | Isotonic agent |
Clinicians should follow the manufacturer’s guidance for reconstitution and administration. As with this class, common post-injection events can include localized pain, bruising, or temporary muscle weakness. Review the package insert and your clinic’s protocols for contraindications, precautions, and reporting processes.
Packaging & Supply
The pack contains a single Nabota 200 Units vial intended for professional use. Pack configuration: 1 vial per pack. Reference SKU: 89767. Labels display lot and expiry to support documentation and inventory systems.
Clinics often allocate one vial per booked procedure slot or provider block to simplify tracking. When building stock plans, consider upcoming sessions, training needs, and buffer inventory for rescheduling. If you require a smaller unit content for specific sessions, review the related 100 U Vial for assortment planning.
Ordering & Logistics
Account verification is required. After approval, sign in to view volume and contract tiers, submit purchase orders, and schedule shipments. Allocation for Nabota botulinum toxin 200 Units follows demand, compliance checks, and warehouse availability. Lead times may vary.
Your orders ship with temperature-controlled handling when required and tracked US delivery. For operational continuity, many clinics set reorder points tied to calendar-based clinics or minimum-on-hand levels. If your workflow uses ancillary supplies, align delivery windows with needles, syringes, and disinfectants to streamline setup.
Comparable Products
Clinics often cross-evaluate this class with other established neurotoxins. For comparison within portfolio and labeling contexts, review Xeomin and Dysport. Selection typically depends on provider familiarity, training protocols, and patient scheduling requirements.
Pricing & Access
Sign in to access current pricing, request quotes, and review contract tiers for multi-case purchasing. Facilities operating multi-location service lines can consolidate demand for negotiated terms. If your acquisition process requires documented alternatives, your account manager can provide comparable SKUs for committee review.
Clinics may choose to Buy botulinum toxin A 200U under an approved account and supply policy. Unit availability and allocation windows may vary by warehouse and seasonality.
Availability & Substitutions
Supply can vary based on manufacturer production and regional demand. If you anticipate schedule expansion or training cohorts, we recommend establishing forecasted needs with your representative. Confirm substitutions with your medical director to ensure continuity of protocols and documentation.
For broader context on neurotoxin choices and planning considerations, see our concise Treatment Guide covering class fundamentals, unit considerations, and portfolio positioning.
Authoritative Sources
- FDA: Botulinum Toxins Overview
- MedlinePlus: Botulinum Toxin Type A (Class Resource)
- Daewoong Pharmaceutical (Manufacturer)
Ready to streamline your neurotoxin inventory? Sign in to request allocation, view contract tiers, and align shipments with your clinic schedule.
Frequently Asked Questions
What is the composition of this vial?
The vial contains botulinum toxin type A at 200 Units as the active component. Excipients include human serum albumin (0.5 mg) as a stabilizer and sodium chloride (0.9 mg) as an isotonic agent. This composition supports reconstitution and professional injection workflows. Always follow the manufacturer’s instructions, clinic SOPs, and applicable regulations for preparation, administration, and documentation.
How should clinics handle storage and preparation?
Follow the product label and the manufacturer’s handling instructions. Use aseptic technique for reconstitution and ensure that only qualified personnel prepare and administer injections. Maintain appropriate chain-of-custody and record lot and expiry in patient charts. If your facility has temperature monitoring or quarantine steps for biologics, align them with your SOPs and the labeling for this specific item.
Who is authorized to administer this product?
Administration should be limited to licensed healthcare professionals acting within their scope of practice and state regulations. Supervising physicians or medical directors typically establish protocols, training, and oversight. If using Nabota during training, ensure competency sign-offs, informed consent processes, and post-procedure monitoring are in place per your organization’s clinical governance framework.
What are common post-injection events to monitor?
As with this class, localized injection-site pain, swelling, bruising, and temporary muscle weakness can occur. Transient headache or eyelid heaviness have been reported with neurotoxin procedures. Review the package insert for contraindications and precautions, and advise patients per clinic policy. Report adverse events through appropriate channels and retain documentation for your quality system.
Can this be used alongside other aesthetic treatments?
Many clinics schedule neurotoxin sessions alongside complementary procedures, such as dermal fillers or skin treatments, based on patient plans and provider judgment. Coordinate timing and sequencing per manufacturer guidance and your medical director’s protocols. Document products, lots, and sites when combining treatments, and provide appropriate post-care instructions per clinic policy.
What documentation accompanies the product?
Each pack includes a labeled vial with lot and expiry. Most shipments include a packing slip and, where applicable, the manufacturer insert. Record the lot, expiry, and treatment details in your EHR or paper chart. Many clinics also maintain inventory logs for reconciliation and recall readiness as part of their quality and safety processes.
How does it compare with other botulinum toxins?
Within the same class, differences may include unit definitions, excipient profiles, approved indications by market, and preparation steps. Provider familiarity and patient scheduling often guide selection. When evaluating alternatives, consider training, documentation, and inventory alignment across sites. Compare with established options such as Xeomin or Dysport, and standardize your workflows accordingly.
Specifications
- Main Ingredient: Botulinum Toxin Type A
- Manufacturer: DAEWOONG PHARMACEUTICAL CO. LTD
- Drug Class:
- Generic Name: Botulinum Toxin Type A
- Package Contents: 200 U x 1 Vial
- Storage Requirements: Cool Temperature (2℃~8℃)
- Main Usage:
About the Brand
NABOTA
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