What is the form and route for this product?

This item is supplied as a sterile, lyophilized botulinum toxin type A powder in a single-use vial. After proper reconstitution per labeling, it is administered intramuscularly by trained professionals using established injection techniques. LETYBO is positioned for aesthetic workflows involving targeted facial muscles, with clinic protocols guiding dilution, anatomical mapping, and procedural sequencing. Always follow the manufacturer’s instructions and your facility’s policies when preparing and administering neurotoxin products.

How is reconstitution handled within clinic workflows?

Reconstitution should follow the product labeling and your clinic’s standard operating procedures. Use aseptic technique, appropriate syringes, and sterile diluent as specified by the manufacturer. Prepare the vial at the procedure station or a designated medication area with proper checks for lot, expiry, and visual integrity. Do not provide patient-specific dosing guidance here; defer to the prescribing clinician and the product insert for exact preparation and administration details.

What comes with the English-labeled package?

The English-labeled configuration includes a single lyophilized vial in a carton with an English package insert and vial label. This helps streamline training and reduces interpretation errors across teams. Lot number and expiration date are displayed on the carton and vial for traceability. Clinics should confirm shipment contents match purchase documentation before stocking and record the lot/expiry during intake to support reconciliation and inventory rotation.

How should storage and handling be approached in clinics?

Follow the storage and handling conditions stated on the carton and insert. Maintain environmental controls and secure storage consistent with your facility’s medication management policies. Keep vials in their original packaging until preparation, and monitor expiry dates during inventory rotation. When transporting between sites or rooms, use appropriate controls to maintain labeled conditions. Discard any vial that shows compromised packaging, labeling issues, or visual integrity concerns.

Can this product be used alongside other aesthetic injectables?

Combination approaches are common in aesthetic practice, but sequencing and selection should be determined by the treating clinician. Many clinics coordinate neuromodulators with dermal fillers or skin boosters in staged sessions. Review each product’s labeling for indications and cautions, and document a plan that aligns with your patient’s goals and safety considerations. Maintain clear treatment records for timing, sites, and products used to support continuity of care and follow-up.

What documentation supports traceability for each vial?

The outer carton and vial label display the lot number and expiry date. Retain invoices, packing slips, and any supplier documentation for your pharmacy records. At receipt, record lot and expiry, reconcile counts, and place vials into the appropriate storage location. Before preparation, verify the vial identity and lot again, documenting usage in the patient or procedure record according to your facility’s policies and regulatory requirements.

How does this compare to other botulinum toxin products?

All products in this class share the core mechanism of action but differ in formulation details, labeled indications, and preparation steps. Clinics evaluate factors such as vial format, language on the carton and insert, and internal experience with handling and reconstitution. Some facilities trial alternatives to standardize workflow. For broader context, review independent resources and compare with internal outcomes before adjusting protocols.

Pharmaceuticals

LETYBO® 50u (English)

LETYBO® 50U Vial for Clinics

Name: LETYBO® 50U Vial – Professional Clinic Supply
SKU: 100147
Price: 157.99 USD
Availability: InStock

Botulinum Toxin

$157.99

Description

LETYBO® is a botulinum toxin type A preparation supplied as a sterile, lyophilized powder for reconstitution and intramuscular administration by trained professionals. Clinics use this product to support aesthetic protocols that address dynamic facial lines with controlled, localized chemodenervation. Available via US distribution for predictable procurement. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.

What LETYBO Is and How It Works

This product is a prescription neurotoxin formulated for intramuscular injection after proper reconstitution. By modulating acetylcholine release at the neuromuscular junction, it can reduce targeted muscle activity to support smoother facial animation patterns. The class has a long record of professional use, with dosing, dilution, and injection techniques guided by labeling and clinic protocols.

The vial is engineered for precise handling and consistent reconstitution characteristics, fitting standard injector workflows in dermatology and aesthetic medicine. The product is listed as Letybo 50u injection on English-language materials, supporting straightforward staff training and documentation. For a broader view of the toxin class, see our Botulinum Toxin category.

Professional Applications

Clinics integrate this preparation into facial aesthetics workflows for glabellar complex work, frontalis patterns, and lateral canthal lines, as clinically appropriate. It supports repeatable appointment sequencing, with scheduling aligned to each clinic’s assessment standards. Treatment plans should be tailored by a qualified injector, incorporating facial assessment, patient goals, and risk management practices.

For inventory planning and program standardization, Letybo 50u clinic supply helps align labeling and documentation across teams. For clinical overviews of toxin use and considerations, review Xeomin Uses and patient-experience topics such as Post-Botox Headaches.

Key Features

Botulinum toxin type A: Neurotoxin for localized chemodenervation.
Lyophilized powder: Reconstitute for intramuscular administration.
Reliable handling: Supports precise dilution and draw-up protocols.
English labeling: Carton and insert in English for staff clarity.
Consistent performance: Built for reproducible clinic workflows.
Sterile production: Manufactured to stringent quality standards.
Labeled strength: LetibotulinumtoxinA 50 Units.
Single-vial format: Efficient item-level control and tracking.

Benefits in Practice

This product integrates smoothly into high-throughput schedules, supporting consistent technique and documentation at the chair. Teams can standardize reconstitution and injection station setup, streamlining turnover and inventory checks. The English insert helps reduce interpretation errors and keeps training simple for rotating staff.

Clinics appreciate the reliable presentation and familiar vial configuration, which fit common sterile prep and syringe workflows. The clear carton and insert assist with onboarding new injectors and maintaining in-service alignment across the team. For teams aligning aesthetics with other modalities, see our Injectables selection and our overview article Innotox Overview.

When standardizing form factors across multiple rooms, Letybo 50u English packaging can aid quick visual verification, minimizing time spent cross-checking language variants. The single-vial format is also practical for session-based requisitions and controlled waste documentation.

Composition & Ingredients

The LetibotulinumtoxinA 50u vial is formulated with the active neurotoxin complex and stabilizing components per the manufacturer’s specification. Composition includes:

Botulinum toxin type A (50 units)
Human serum albumin
Sodium chloride

These ingredients reflect a typical class formulation for aesthetic indications. For adjacent product classes used in clinic programs, browse Pharmaceuticals.

Packaging & Supply

The package includes one vial of lyophilized neurotoxin powder for reconstitution prior to intramuscular use. The carton, vial label, and insert are in English for staff clarity. Labels provide standard lot number and expiry date information for traceability. The stocked configuration supports counting, rotation, and reconciliation within common inventory systems.

Clinics seeking a clear item description can reference SKU 100147. For teams documenting inventory, the description aligns with Letybo 50 Units vial and standard English-language packaging. The labeled strength is visible on the carton and vial to streamline checks during receiving and before preparation at the injection station.

Ordering & Logistics

Create or verify your business account to view available packs and request volume or contract pricing. Licensed facility details may be required for access. Your account dashboard simplifies reorders, lot tracking notes, and documentation downloads where applicable.

Orders are processed through our vetted distributor network. We provide pack visibility, order confirmations, and tracking updates to help you align schedules and staff time on procedure days. Sign in to see live availability and add this item to your clinic formulary list.

Comparable Products

Clinics comparing toxin options may also evaluate alternatives in the same class, such as Innotox 50U or Kaimax 200U, based on their internal protocols and patient mix.

Pricing & Access

Sign in to view current pricing and packaging options. Volume and contract pricing tiers are available for qualified accounts. Your account manager can assist with formulary alignment and multi-site planning without disrupting established protocols or supply review cycles.

Availability & Substitutions

Supply may vary by lot and distributor intake. If the requested item is temporarily constrained, your account manager can help identify suitable class alternatives for your protocol, pending your clinical approval. Confirm substitutions with your team before updating treatment plans or staff training materials.

Authoritative Sources

For additional context on botulinum toxin products and class guidance, see the FDA’s overview of Botulinum Toxin Products and the NIH’s MedlinePlus: Botulinum Toxin Injection. Manufacturer background is available at Hugel.

Ready to align your inventory? Sign in to source this item with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

What is the form and route for this product?
This item is supplied as a sterile, lyophilized botulinum toxin type A powder in a single-use vial. After proper reconstitution per labeling, it is administered intramuscularly by trained professionals using established injection techniques. LETYBO is positioned for aesthetic workflows involving targeted facial muscles, with clinic protocols guiding dilution, anatomical mapping, and procedural sequencing. Always follow the manufacturer’s instructions and your facility’s policies when preparing and administering neurotoxin products.
How is reconstitution handled within clinic workflows?
Reconstitution should follow the product labeling and your clinic’s standard operating procedures. Use aseptic technique, appropriate syringes, and sterile diluent as specified by the manufacturer. Prepare the vial at the procedure station or a designated medication area with proper checks for lot, expiry, and visual integrity. Do not provide patient-specific dosing guidance here; defer to the prescribing clinician and the product insert for exact preparation and administration details.
What comes with the English-labeled package?
The English-labeled configuration includes a single lyophilized vial in a carton with an English package insert and vial label. This helps streamline training and reduces interpretation errors across teams. Lot number and expiration date are displayed on the carton and vial for traceability. Clinics should confirm shipment contents match purchase documentation before stocking and record the lot/expiry during intake to support reconciliation and inventory rotation.
How should storage and handling be approached in clinics?
Follow the storage and handling conditions stated on the carton and insert. Maintain environmental controls and secure storage consistent with your facility’s medication management policies. Keep vials in their original packaging until preparation, and monitor expiry dates during inventory rotation. When transporting between sites or rooms, use appropriate controls to maintain labeled conditions. Discard any vial that shows compromised packaging, labeling issues, or visual integrity concerns.
Can this product be used alongside other aesthetic injectables?
Combination approaches are common in aesthetic practice, but sequencing and selection should be determined by the treating clinician. Many clinics coordinate neuromodulators with dermal fillers or skin boosters in staged sessions. Review each product’s labeling for indications and cautions, and document a plan that aligns with your patient’s goals and safety considerations. Maintain clear treatment records for timing, sites, and products used to support continuity of care and follow-up.
What documentation supports traceability for each vial?
The outer carton and vial label display the lot number and expiry date. Retain invoices, packing slips, and any supplier documentation for your pharmacy records. At receipt, record lot and expiry, reconcile counts, and place vials into the appropriate storage location. Before preparation, verify the vial identity and lot again, documenting usage in the patient or procedure record according to your facility’s policies and regulatory requirements.
How does this compare to other botulinum toxin products?
All products in this class share the core mechanism of action but differ in formulation details, labeled indications, and preparation steps. Clinics evaluate factors such as vial format, language on the carton and insert, and internal experience with handling and reconstitution. Some facilities trial alternatives to standardize workflow. For broader context, review independent resources and compare with internal outcomes before adjusting protocols.

Specifications

Main Ingredient: Botulinum Toxin A
Manufacturer: Hugel Inc.
Drug Class: Aesthetic Dermatology
Generic Name: Botulinum Toxin Type A
Package Contents: 1 vial
Storage Requirements: Cool Temperature (2℃~8℃)
Main Usage: Fine Lines

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