Description
What Nabota Is and How It Works
Nabota® is a botulinum toxin type A preparation supplied as a sterile, vacuum-dried powder for reconstitution and intramuscular administration by trained professionals. Clinics use this neuromodulator to support aesthetic protocols and select neurology service lines in adults. We support US distribution for credentialed accounts.
Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
Mechanistically, the neurotoxin inhibits acetylcholine release at cholinergic terminals, producing a temporary, localized reduction in muscle activity. The vial is reconstituted per manufacturer guidance prior to intramuscular use by qualified injectors. Within this line, Nabota 100 U denotes a single-use vial labeled for unit-calibrated activity to support standardized clinic workflows.
Professional Applications
In aesthetic workflows, teams deploy this agent for upper-face rhytid protocols across glabellar, lateral canthal, and forehead regions in appropriate adults, following clinic policy and training. As a Nabota 100U injectable, it fits neuromodulator services that rely on consistent vial potency and reproducible preparation steps.
Neurology programs may integrate the product into chronic migraine prevention pathways where botulinum toxin type A is utilized under specialist oversight. For a broader view of neurotoxin options used in professional settings, see the Botulinum Toxins category.
Key Features
- Clinic-focused format: sterile, vacuum-dried powder for reconstitution and intramuscular administration.
- Consistent unit standard: calibrated vial supports reproducible dilution and mapping across providers.
- Controlled excipients: human serum albumin and sodium chloride formulated for isotonicity.
- Unit strength: Botulinum toxin type A 100U vial format.
- Clear labeling: lot number and expiration date visibly printed for inventory checks.
- Streamlined pack: single vial per pack reduces partials and simplifies count accuracy.
- GMP manufacturing: produced to quality standards suitable for clinical procurement.
- Expected reactions: temporary localized weakness, injection-site pain, and bruising may occur.
Benefits in Practice
This product integrates smoothly into aesthetic and neurology schedules, supporting consistent preparation steps and predictable handling. Teams can establish standardized dilution and mapping protocols, which helps reduce variance across sessions and staff.
Single-vial packaging enables straightforward stock rotation and minimizes opened multi-vial waste. Clear unit labeling aids audit trails and treatment sheet documentation. The composition supports reliable reconstitution behavior, which helps maintain timing and chair flow.
For clinical teams reviewing brand comparisons and treatment planning context, see Top Toxins. For adjunct supply planning, review our guide on sharps and accessories in Cannulas & Needles.
Composition & Ingredients
- Active component: Clostridium botulinum toxin type A, 100 Units per vial.
- Stabilizing agent: Human serum albumin 0.5 mg.
- Isotonic agent: Sodium chloride 0.9 mg.
The preparation is preservative-free. Each vial is vacuum-dried and requires reconstitution with an appropriate diluent before intramuscular administration by trained professionals. In procurement documentation, this product may appear as Nabota 100U botulinum toxin for identification purposes.
Commonly reported adverse reactions include temporary muscle weakness near the injection site, mild to moderate injection-site pain, and bruising. As with all neuromodulator products, adverse effects can vary by dose, muscle selection, and technique. Clinicians should follow institutional protocols and refer to the product literature for complete safety information.
Packaging & Supply
Pack configuration: 1 vial per pack. The vial is labeled for 100 Units of activity. SKU: 89766. Lot and expiry are printed on primary and/or secondary packaging to support inventory control and documentation. No administration supplies are included.
Clinics seeking the same class at higher unit count can review Nabota 200 U for larger session planning. Maintain storage and handling in accordance with the manufacturer’s instructions and your facility’s medication management policies.
Ordering & Logistics
Licensed accounts can sign in to view contract and volume tiers. New customers should submit credentials for verification before purchasing. For formulary restocks, purchase orders, or EDI ordering can be coordinated with our team. Facilities planning a Nabota 100U bulk order can contact account services to align replenishment schedules with clinic volumes.
For broader procurement across therapeutic areas, browse Pharmaceuticals to consolidate category picks, streamline receiving, and simplify invoicing under one account.
Comparable Products
Clinics often compare options within the same therapeutic class. Consider Dysport for an alternative presentation and unit schema. For another established option in this class, review Neurotoxin Option as part of your formulary assessment and staff training plans.
Pricing & Access
Sign in to view current pricing and available tiers. We support clinic-level volume programs and contract terms for multi-site groups, with options to align order frequency and invoice cycles to your service calendar. Your account manager can help coordinate documentation for compliance review and product onboarding.
Availability & Substitutions
Supply may vary based on manufacturer production and channel allocations. If this item is limited, work with your account manager to confirm suitable substitutions within the same class and review labeling, unit references, and injector training impacts before adopting alternatives. We do not guarantee restock timelines; please plan inventory with buffer lead time where possible.
Authoritative Sources
- FDA: Botulinum Toxin Overview
- NIH MedlinePlus: Botulinum Toxin Type A
- NCBI: Botulinum Toxin—Clinical Use and Safety
Ready to source for your licensed facility? Sign in to add to your formulary with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
What is the form and route of this product?
This product is a sterile, vacuum-dried botulinum toxin type A powder supplied in a single-use vial for reconstitution. After dilution according to clinic policy and product literature, trained professionals administer it by intramuscular injection. The preparation is preservative-free and includes human serum albumin and sodium chloride as excipients. Use only within licensed healthcare settings and maintain documentation consistent with facility medication management procedures.
How should clinics handle reconstitution?
Follow the manufacturer’s instructions and your facility’s standard operating procedures. Reconstitute using an appropriate diluent under aseptic technique, label the syringe and vial as required, and document the lot and expiry. Avoid shaking vigorously once reconstituted. Prepare and administer within time windows defined by your policy. Only trained clinicians should reconstitute and inject neuromodulators, and all sharps must be handled and discarded per institutional and local regulations.
What storage conditions are typical?
Refer to the product label for exact storage conditions and shelf-life. Maintain secure medication storage that aligns with your facility’s temperature monitoring and access control policies. Keep vials in original packaging until use to protect from light and to preserve label information. Do not use if the vial or seal is compromised. Always track lot numbers and expiry dates in your inventory system for full traceability.
Which adverse reactions are most reported?
Commonly reported events include temporary localized muscle weakness, injection-site pain, and bruising. Less frequent reactions may relate to spread of effect or hypersensitivity. Actual incidence depends on injected muscles, dose, and technique. Counsel recipients consistent with your clinic’s consent process, and review the official product literature for comprehensive safety and post-procedure guidance. Monitor patients after treatment per your institutional protocols.
Can this product be used across different service lines?
Yes, clinics may integrate botulinum toxin type A into aesthetic workflows for upper-face rhytids and into neurology pathways such as chronic migraine prevention, in line with labeling and institutional policies. Coordination between medical directors and injectors helps standardize dilution, mapping, and follow-up. Confirm competency, scope, and documentation standards for each service line before scheduling sessions.
What documentation is required to order?
We supply licensed healthcare entities. New accounts typically provide clinical licensure, tax documentation, and authorized purchaser details. After verification, you can sign in to view pricing, submit purchase orders, and set delivery preferences. Multi-site groups may add ship-to locations under a master account. Contact account services if your facility requires vendor packet completion or specific invoicing formats.
Do you offer substitutes if stock is limited?
Stock levels can vary. If this item is constrained, your account manager can suggest suitable alternatives within the same class for review by your medical director. Evaluate labeling, unit references, injector training, and appointment scheduling impacts before adopting substitutions. We do not guarantee restock timelines, so plan buffer inventory where appropriate and consider cross-listing a secondary option in your formulary.
Specifications
- Main Ingredient: Botulinum Toxin Type A
- Manufacturer: DAEWOONG PHARMACEUTICAL CO. LTD
- Drug Class:
- Generic Name: Botulinum Toxin Type A
- Package Contents: 100 U x 1 Vial
- Storage Requirements: Cool Temperature (2℃~8℃)
- Main Usage:
About the Brand
NABOTA
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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