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Description
Re N Tox® is a botulinum toxin type A powder for injection in a 100U vial. Licensed professionals use it to relax targeted facial muscles and soften dynamic lines; available through US distribution to verified accounts. 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 preparation is a purified neuromodulator intended for intramuscular administration by trained providers. It acts at the neuromuscular junction by inhibiting acetylcholine release, which reduces targeted muscle activity. The effect supports temporary softening of dynamic lines in common upper-face regions.
As a Botulinum Toxin product, it integrates into aesthetic protocols that prioritize precision and repeatability. Many clinics select a 100 Unit botulinum toxin vial format to align with standard unit planning and appointment timing. Use is restricted to licensed professionals; follow the manufacturer’s instructions for reconstitution and administration techniques.
Professional Applications
Clinics deploy this neuromodulator within facial aesthetics programs that emphasize targeted muscle relaxation for the upper face. Typical workflows include glabellar, frontalis, and lateral canthus protocols, with unit mapping aligned to the clinic’s technique standards. It can also be incorporated into combination strategies alongside dermal fillers, energy-based devices, or skin-quality treatments when appropriate.
For therapeutic positioning within an aesthetic framework, providers may categorize it under Botulinum toxin A 100U therapeutic scheduling to coordinate patient follow-ups and retreatment intervals. Practices standardize photography, consent, and documentation to support reproducible results across sessions. For brand-specific documentation and marketing assets, see our Brand Page.
Key Features
- Type A neuromodulator: supports targeted muscle relaxation.
- Single-use sterile vial: vacuum-dried powder for injection.
- Traceable labeling: visible lot number and expiry for charting.
- Flexible integration: compatible with common aesthetic workflows.
- Professional-only product: administration by licensed providers.
- Quality focus: sourced through vetted channels for clinic use.
- Clinic-ready format: Botulinum toxin type A 100 Units vial for standardized unit planning.
- Storage per label: handle and store according to manufacturer guidance.
For an overview of other neurotoxins used in practice, review Popular Neurotoxins.
Benefits in Practice
- Predictable scheduling: supports consistent appointment lengths and retreatment planning.
- Inventory efficiency: unit-based vial aligns with common billing and stock controls.
- Team training: straightforward workflow aids staff competency and handoffs.
- Charting clarity: clear unit counts simplify documentation and reconciliation.
- Versatile protocols: appropriate for upper-face aesthetic programs under medical oversight.
- Patient experience: steady performance profile supports consultation discussions.
- Cosmetic positioning: aligns with Botulinum toxin A 100U cosmetic treatment pathways in many practices.
Composition & Ingredients
The active ingredient is botulinum toxin type A. This is supplied as a neuromodulator powder for reconstitution and intramuscular injection by trained professionals. Clinics use Re N Tox 100U powder for injection as part of standardized aesthetic protocols. Inactive components and stabilizers, if present, are detailed in the manufacturer’s prescribing information. Refer to the official insert for a full ingredients list and handling instructions.
Packaging & Supply
This line is supplied as a single-use, vacuum-dried powder for injection in a labeled vial. For inventory control and charting, the vial and carton display lot and expiration details clearly. Many clinics maintain barcode capture to streamline intake and documentation.
The Re N Tox 100U vial format supports unit-based planning and consistent workflow design. Proper dilution is required prior to administration; follow the manufacturer’s guidance. Product SKU for this listing: 89693. Storage and handling must follow the labeled instructions and your facility’s policies.
Ordering & Logistics
Account verification is required. Sign in to view volume or contract tiers aligned to your clinic’s purchasing profile. Our team supports group practices and multi-site organizations with coordinated fulfillment options. Place orders through your verified account to enable order history, invoices, and reorder efficiency.
This is a prescription product intended for professional administration only. Clinics should follow applicable regulations and manufacturer recommendations for dilution, injection technique, and documentation. Packaging integrity should be inspected on receipt; do not use if seals or vials are compromised.
Comparable Products
Clinics that stock this neuromodulator often evaluate alternatives within the same class. Consider the 200U Option for higher-volume protocols. Many practices also compare with Xeomin to standardize across patient cohorts and technique preferences. For another benchmark in this category, see our Toxin Comparison. For brand-level insights, read Xeomin vs Dysport.
Pricing & Access
Sign in with a verified clinic account to view pricing. Volume-based and contract tiers are available for qualified purchasers. If your facility operates under a centralized procurement model, contact our team for coordinated account mapping and site-level access. Quotes for recurring supply or multi-site coverage can be arranged on request.
Availability & Substitutions
Availability can vary by lot and shipment window. When a preferred unit size is limited, our team can suggest comparable neuromodulators from the same class for evaluation. Confirm any substitutions with your medical director and staff trainers to maintain technique consistency across providers and locations. We do not guarantee restock dates; please plan inventory levels according to your clinic’s booking patterns.
Authoritative Sources
Review independent resources for class-level information and safety guidance:
Ready to add this product to your formulary? Sign in to request supply with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
What clinical format is supplied with this product?
It is supplied as a sterile, single-use powder for injection in a sealed vial. The vial and carton show the lot number and expiry date for traceability. Proper dilution is required before administration according to the manufacturer’s instructions. Store and handle per label requirements. Inspect packaging on receipt and do not use damaged or compromised vials. This presentation is intended for professional use in licensed healthcare settings.
Which providers can administer treatments with this neuromodulator?
Administration is limited to licensed healthcare professionals working within their scope of practice and local regulations. Clinics typically authorize trained physicians, physician assistants, nurse practitioners, or registered nurses under appropriate supervision. Each facility should maintain credentialing, training, and competency documentation for injectors and adhere to established protocols for patient assessment, consent, and post-treatment follow-up.
How should the vial be stored and handled?
Follow the manufacturer’s labeling for storage, handling, and stability. Maintain appropriate temperature control as directed on the package and avoid using products with compromised seals or unclear labeling. Upon receipt, verify lot and expiry, then secure vials in a restricted, monitored area. Do not re-use single-use vials. Your clinic’s policies should cover chain-of-custody procedures and inventory reconciliation for neuromodulators.
Is a diluent included with the vial?
A separate diluent is typically required and is not included with the vial. Use the appropriate sterile diluent according to the manufacturer’s instructions and your medical director’s protocol. Prepare the product immediately prior to administration and observe aseptic technique. Do not provide or follow dosing instructions outside the approved labeling and your clinic’s established procedures.
Can this product be combined with other aesthetic treatments?
Many clinics coordinate neuromodulator sessions with complementary procedures such as dermal fillers, energy-based devices, or skin-quality treatments. Sequencing and timing should be individualized based on the medical assessment and your practice’s protocols. Document pre- and post-treatment guidance, and plan follow-up visits according to your standard operating procedures. Always follow applicable regulations and manufacturer recommendations.
How does this compare with other botulinum toxin brands?
Products in this class share a common neuromodulation mechanism but may differ in unit equivalence, labeling, formulation, or handling instructions. Clinics typically choose based on injector preference, training, and consistency across patient cohorts. If you are evaluating alternatives, consider comparable brands like Xeomin or Dysport and review your internal technique maps prior to substitution to maintain predictable outcomes.
What documentation is provided for compliance and records?
Shipments include labeled packaging with lot and expiry for traceability. Your order history and invoices are available in your account portal for reconciliation. Maintain manufacturer inserts with each lot for reference to indications, handling, and safety information. Clinics should integrate these details into their EHR or inventory system to support chain-of-custody tracking and standardized charting across providers.
Specifications
- Main Ingredient: Botulinum Toxin A
- Manufacturer: PHARMA RESEARCH PRODUCTS
- 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
RE N TOX
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