Description
Re N Tox® is a lyophilized botulinum toxin type A powder for injection, supplied as a sterile single-use vial for reconstitution with preservative-free normal saline by qualified clinicians. Clinics integrate this preparation into neuromodulator services and procedural workflows for predictable handling and clarity after dilution, supported by US distribution for verified buyers. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
What Re N Tox Is and How It Works
This botulinum neurotoxin type A preparation arrives as a white lyophilized cake that becomes a colorless, transparent solution after proper dilution with 0.9% sodium chloride. It is intended for intramuscular administration by trained medical professionals working within clinic protocols. On reconstitution, the solution supports precision dosing strategies determined by the provider’s clinical judgment and institutional guidelines.
At the cellular level, this class of neurotoxins can reduce cholinergic transmission at the neuromuscular junction by blocking acetylcholine release. That mechanism underpins its role in aesthetic neuromodulator services and other physician-directed procedures. Details on precise reconstitution and administration are established by institutional SOPs and the professional’s training. In professional parlance, Re N Tox botulinum toxin 200U denotes a lyophilized, unit-based vial designed for dilution to a clear solution.
For additional brand background and related items, visit the Re N Tox Brand page.
Professional Applications
Clinics commonly position this product within aesthetic neuromodulator workflows. Typical use cases include upper-face and periorbital modulation services, lower-face balancing protocols in select patients, and adjunctive roles alongside skin-quality programs. It also fits into training environments where providers refine injection mapping under supervision.
This product can sit alongside practice offerings such as hyaluronic acid fillers, biostimulators, and energy-based devices. Team members can map treatment zones, prepare the vial per protocol, and stage sterile trays for efficient room turnover. For a broader perspective on neuromodulators in the market, see our article Toxin Overview.
As with any injectable, qualified personnel should use aseptic technique and appropriate patient selection. Common post-procedure reactions may include localized pain, erythema, edema, or bruising; infrequent events such as eyelid ptosis, eyebrow asymmetry, or dry/watery eyes can occur. Monitor patients per clinic policy and counsel them on expected time courses and follow-up.
Key Features
- Lyophilized format: stable white cake that reconstitutes to clear solution.
- For injection: prepared with preservative-free normal saline per protocol.
- Single-use vial: supports sterile handling and controlled draw-up.
- Professional route: intended for intramuscular administration by trained clinicians.
- Quality focus: produced under modern manufacturing and release controls.
- Label clarity: lot number and expiry date printed for traceability.
- Workflow fit: compatible with common neuromodulator service lines.
- Inventory ready: packaged for straightforward storage and counting.
For a broader selection of clinical medicines and injectables, explore Pharmaceuticals.
Benefits in Practice
- Efficient preparation: straightforward reconstitution steps fit routine trays.
- Clear solution: visual confirmation supports confident draw-up and labeling.
- Predictable handling: consistent vial format eases staff training.
- Inventory control: single-vial packaging streamlines counts and reorders.
- Flexible scheduling: supports same-day consult-to-service workflows.
- Team alignment: integrates with established SOPs and QA processes.
- Procedure synergy: complements fillers, skin boosters, and threads.
- Documentation ease: clear lot/expiry aids charting and recalls.
Composition & Ingredients
Active substance: Clostridium botulinum toxin type A (strain CBFC26).
Excipients: The manufacturer specifies stabilizers and formulation components on the official label. Full excipient details may vary by lot and are available on-package. The recommended diluent for preparation is preservative-free 0.9% sodium chloride (not included in the vial).
Upon reconstitution, the solution should appear colorless and transparent. Follow your institution’s policies for handling, labeling, and post-reconstitution timing to maintain product integrity and patient safety.
Packaging & Supply
This item is supplied as a single glass vial in an individual carton. Each Botulinum toxin type A 200 Units vial is provided one per box with tamper-evident closure. The label includes the product name, lot number, and expiry date for streamlined receiving and documentation. The vial contains a white lyophilized powder that becomes a clear solution after addition of preservative-free normal saline.
Pack configuration: 1 vial per box. SKU: 89694. Cartons are suitable for shelf storage in accordance with label guidance. Your team can scan the lot at receiving and record it in your EMR, EHR, or inventory system for traceability and controlled rotation.
For additional clinic-use medicines, browse Pharmaceuticals.
Ordering & Logistics
Account verification is required for clinic access. Sign in to view available packs and current procurement options. Qualified buyers may request quotes for larger volumes or contract terms through their account manager. Orders placed during business hours typically confirm quickly, and shipment status updates are provided through your dashboard and email notifications.
To support efficient operations, we coordinate fulfillment with vetted distribution partners and maintain documentation for lot traceability. If your facility uses centralized receiving, include PO numbers on checkout for streamlined reconciliation. For operational consistency, align delivery windows with staff availability to secure prompt receipt and inspection.
Comparable Products
Clinics often evaluate multiple neuromodulators to match patient profiles and scheduling needs. Consider Alternative Dysport and Compare Xeomin as peer options within this category. Practices that cross-train teams on more than one brand may streamline coverage when demand fluctuates. For a broader market perspective on brand characteristics, see our Neuromodulator Comparison or review additional Aesthetic Toxins available in the catalog.
Pricing & Access
Sign in to view clinic pricing, eligibility for volume tiers, and contract options. Facilities purchasing across multiple departments can discuss consolidated terms with their representative. Quotes can reflect order frequency, shipment consolidation preferences, and documentation requirements. If your supply plan includes training or onboarding, let us know so we can align timing with your education calendar.
Availability & Substitutions
Supply can vary based on manufacturing cycles and regional demand. If a planned procurement is time-sensitive, confirm timing with your account manager before scheduling patients. When substitution is necessary, evaluate comparable neuromodulators against your clinic’s protocols, availability of injectors trained in each product, and packaging preferences. Maintain consistent charting for lot and expiry across brands to preserve traceability and patient safety.
Authoritative Sources
- NIH MedlinePlus: Botulinum Toxin Information
- CDC: Clinical Overview of Botulism and Toxins
- FDA: Botulinum Toxin Products (Class Overview)
Ready to align inventory with upcoming clinics? Sign in to schedule procurement with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
What format is the vial and how is it prepared?
The vial contains a sterile lyophilized powder that becomes a clear, colorless solution after reconstitution with preservative-free 0.9% sodium chloride. Preparation and administration are performed by trained professionals following clinic SOPs. Labeling should include lot and expiry for traceability. The product name may appear on purchase documents as Re N Tox™ 200 U, which reflects the unit-based vial supplied to clinics.
Which professionals are qualified to administer this neurotoxin?
Administration should be limited to licensed medical professionals who are trained in neuromodulator techniques and institutional protocols. Scope of practice varies by jurisdiction, but typically includes physicians, physician assistants, nurse practitioners, and qualified registered nurses acting under appropriate supervision. Teams should follow aseptic technique, maintain detailed documentation, and provide patient counseling on expected timelines and routine post-injection care.
How should clinics plan inventory for a neuromodulator vial?
Plan inventory around your appointment cadence, injector availability, and anticipated service mix. Keep buffer stock to accommodate reschedules and training sessions. Align orders with delivery windows so receiving staff can promptly inspect and log lots. If your clinic consolidates purchases, coordinate cycle dates and build in contingency coverage. Some practices also evaluate Re N Tox 200U bulk order options through their account manager when volumes increase seasonally.
What reactions or adverse events should staff review with patients?
Common post-injection reactions may include transient pain, tenderness, erythema, edema, or bruising at the injection site. Less common events can include headache, eyelid droop, eyebrow asymmetry, or dry/watery eyes. Infection at the injection site, although uncommon with aseptic technique, is possible. These are class-related considerations for neuromodulators. The Re N Tox 200U injectable should be used by qualified clinicians who can evaluate risk factors and provide appropriate follow-up guidance.
How does your team verify authenticity and traceability?
We source via vetted distributors and inspect inbound lots for seal integrity, label quality, and documentation. Cartons display lot numbers and expiry dates to support receiving logs and charting. Facilities can request supporting paperwork when required for internal QA. For clinics seeking assurance, our workflow emphasizes tamper-evident packaging and chain-of-custody controls so your team receives Re N Tox 200U authentic product through a professional supply channel.
Does this product integrate with established clinic protocols?
Yes. The vial’s lyophilized format, clear labeling, and straightforward reconstitution steps align with standard neuromodulator workflows. It integrates with common room setups, sterile tray assembly, and documentation routines. Teams can segment dosing across mapped facial or cervical zones per protocol. When evaluating the Botulinum toxin type A 200 Units vial against alternatives, many clinics focus on inventory fit, labeling clarity, and staff familiarity rather than brand preference alone.
What alternatives are suitable if this item is temporarily unavailable?
If this item is back-ordered or allocated, consider other neuromodulators within the same class that fit your team’s training and patient mix. Cross-train staff on comparable products so scheduling remains flexible. Review unit counts, vial format, and labeling when planning substitutions, and keep charting consistent across brands. Discuss timing with your account manager to align shipment windows with clinic sessions and to minimize service interruptions.
Specifications
- Main Ingredient: Botulinum Toxin Type A
- Manufacturer: PHARMA RESEARCH PRODUCTS
- 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
RE N TOX
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