What is the professional use and route of administration?

This product is a sterile, lyophilized botulinum toxin type A intended for intramuscular injection by licensed healthcare professionals. It is reconstituted according to facility protocols and administered to targeted muscles under aseptic technique. Clinical teams typically integrate it into aesthetic workflows for dynamic line modulation or other practice-approved neuromodulator pathways. Ensure appropriate screening for contraindications and adhere to your medical director’s supervision and local regulations.

How should the vial be stored and handled on arrival?

Store unopened vials refrigerated at 2–8°C and protect them from light. Do not freeze. Assign a receiving contact to place the shipment into medical refrigeration without delay. Maintain chain of custody documentation per your facility’s SOPs. Follow the label and your internal policies for reconstitution media, handling time, and post-reconstitution use. Dispose of sharps and unused material per local regulations and institutional guidelines.

Who should not receive this treatment in a clinic setting?

Avoid use in individuals with known hypersensitivity to botulinum toxin components, those with active infection at intended injection sites, or patients with significant neuromuscular disorders unless carefully evaluated by the supervising provider. Limit administration to trained, licensed injectors. Review the product label and institutional criteria for eligibility, including current medications, prior history with neuromodulators, and risk factors relevant to your practice.

What onset and duration should teams anticipate?

Onset and duration vary by individual and injection parameters. Many clinics plan follow-up windows based on typical neuromodulator scheduling for type A toxins, which can support predictable appointment spacing. Avoid definitive claims and counsel conservatively. Photographs and standardized scales can help track changes over time. Coordinate patient check-ins based on your practice’s norms rather than fixed promises.

Can it be combined with fillers, devices, or skin boosters?

Yes, many clinics integrate neuromodulators with dermal fillers, energy-based devices, and topical programs. Space treatments according to your protocols and ensure informed consent reflects the plan. Consider staging to reduce confounding effects during assessment. Coordinate pre- and post-care guidance across modalities so patients receive clear, consistent instructions from all providers involved.

What post-injection guidance is typical after sessions?

Common guidance includes avoiding strenuous exercise, high-heat exposure, and massaging or manipulating treated areas for the first 24 hours. Transient effects like mild swelling, redness, or bruising can occur and generally resolve without intervention. Provide contact details for concerns and schedule follow-up per your practice norms. Document counseling, especially for first-time recipients, to standardize expectations and ensure continuity of care.

How are lot, expiry, and substitutions managed for inventory control?

Each vial’s label displays lot and expiration to support inventory logging and rotation. Align order cadence with your schedule and keep safety stock when feasible. If supply is constrained, review alternatives within the toxin class that fit your practice protocols. Update injector preferences, reconstitution steps, and consent language before substitution to maintain consistency across rooms and minimize variability.

Botulinum Toxins

Botulax® Korean

Botulax® Korean Powder for Injection for Clinics

Botulinum Toxin

Price range: $219.00 through $349.00

Description

Botulax® Korean is a botulinum toxin type A powder intended for intramuscular injection in professional settings. Clinics use it within aesthetic workflows and muscle-modulation protocols where controlled diffusion and consistent performance matter. US distribution supports timely replenishment for procedural scheduling and inventory planning.

What Botulax Is and How It Works

This preparation is a sterile, lyophilized neurotoxin type A supplied for reconstitution and targeted intramuscular administration. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors. As a Botulax powder for injection, the vial is reconstituted according to facility SOPs and injected into selected muscle groups by trained practitioners.

In practice, the active complex acts at the neuromuscular junction, where it can temporarily inhibit acetylcholine release. This mechanism supports softening of dynamic facial lines and other clinic-directed neuromodulator uses. The product’s precise handling characteristics help practitioners plan dosing patterns and customary injection mapping within established protocols.

Professional use only. Restrict administration to licensed injectors trained in botulinum toxin techniques. Screen for hypersensitivity, active infection at intended sites, and clinically significant neuromuscular disorders before scheduling.

Professional Applications

This agent fits aesthetic programs focused on dynamic lines across the upper face and selective lower-face indications assessed by the provider. It also appears in muscle-modulation and sweat-management pathways when appropriate to practice scope. Many facilities integrate Korean botulinum toxin type A in combination plans that may include dermal fillers, energy-based devices, and skincare regimens, with appropriate spacing and clinical judgment.

For a broader view of related agents, explore our Botulinum Toxins category or review market context in Top Botulinum Toxin. For safety considerations and counseling points, see our Side Effects Guide.

Key Features

Type A neurotoxin: Sterile, lyophilized powder
Intramuscular delivery: Targeted administration
Controlled diffusion: Designed for precision placement
Stable composition: Consistent handling profile
Clinic-focused workflow: Predictable reconstitution process
Professional-only product: Licensed injector use
Storage 2–8°C: Refrigerated handling guidance
Clear labeling: Lot and expiry visibility

Benefits in Practice

Clinicians value dependable preparation behavior during reconstitution and measured spread at typical injection depths. That predictability helps maintain injection maps and supports consistent session timing across providers. Scheduling remains efficient when handling and setup steps are familiar to the team.

The product aligns well with established aesthetic pathways. It supports standard consultation flows, photography, and follow-up scheduling. Staff can build repeatable tray setups and maintain streamlined documentation. Post-session guidance commonly includes avoiding strenuous exercise, high-heat exposure, and massaging the treated area for the first 24 hours.

Comfortable handling characteristics aid new staff onboarding and reduce variability across rooms. To aid informed counseling about expected experiences and common temporary reactions such as local swelling or bruising, your team can reference our Side Effects Guide.

Composition & Ingredients

Active ingredient: botulinum toxin type A complex in sterile, lyophilized form. Excipients and stabilizers follow manufacturer specifications; refer to the product’s current label and accompanying documentation for the complete list. The composition is formulated for precision injection after reconstitution with a suitable diluent, under aseptic technique.

No additional agents are included beyond those specified in the packaging insert. Verify local protocols for reconstitution media, needle selection, and intended targets. Use aseptic technique at all times.

Packaging & Supply

This listing references a Botulax toxin type A vial intended for reconstitution prior to intramuscular injection. Each sterile vial is individually labeled with lot number and expiration date to simplify inventory tracking. Outer packaging supports secure handling and storage in a medical refrigerator.

Storage guidance: keep refrigerated at 2–8°C. Do not freeze. Protect from direct light. Maintain chain of custody from receipt to administration under clinic SOPs. Presentation details can vary by lot and market authorization; confirm the specific presentation on your label before integrating into workflow or ordering additional units.

Ordering & Logistics

Create or verify your professional account to request access. Sign in to view available options and submit purchase orders aligned with your facility’s procurement process. Our team can assist with documentation for account setup and regulatory verification as needed.

For fulfillment, we coordinate shipping windows suitable for clinical receiving hours and provide status updates for planning. Temperature-controlled handling may be applied when required by the item’s storage profile. Please allocate a responsible receiving contact and appropriate cold storage upon arrival.

Comparable Products

Clinics evaluating this line often compare it with other A-toxins to align with injector preference and patient scheduling. Related options include Dysport and Xeomin, each with distinct handling and diffusion characteristics. For a side-by-side perspective, see Toxin Comparisons. Clinics expanding combination protocols may also review procedural threads; start with our PDO Threads Guide.

Pricing & Access

Sign in to view Botulax Korean price, eligibility, and procurement preferences for your facility. Contract and volume tiers are available for qualified accounts. Your account manager can help align order cadence with planned treatment calendars and provide documentation to support internal approval workflows.

Availability & Substitutions

Supply can vary by lot and regional authorization. If your preferred presentation is temporarily constrained, our team can discuss suitable alternatives within the class and timeframes for resupply. We prioritize Botulax authentic Korea origin from vetted sources and will confirm product lineage when requested.

When substitutions are considered, verify injector familiarity, reconstitution procedures, and consent language before making a switch. Cross-train staff and update tray checklists to minimize room-to-room variability.

Authoritative Sources

Use these references to support team education and protocol maintenance. Always follow local regulations, your medical director’s guidance, and the product’s official labeling.

Ordering & Logistics Summary

Ready to align inventory with your schedule? Sign in to request supply with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

What is the professional use and route of administration?
This product is a sterile, lyophilized botulinum toxin type A intended for intramuscular injection by licensed healthcare professionals. It is reconstituted according to facility protocols and administered to targeted muscles under aseptic technique. Clinical teams typically integrate it into aesthetic workflows for dynamic line modulation or other practice-approved neuromodulator pathways. Ensure appropriate screening for contraindications and adhere to your medical director’s supervision and local regulations.
How should the vial be stored and handled on arrival?
Store unopened vials refrigerated at 2–8°C and protect them from light. Do not freeze. Assign a receiving contact to place the shipment into medical refrigeration without delay. Maintain chain of custody documentation per your facility’s SOPs. Follow the label and your internal policies for reconstitution media, handling time, and post-reconstitution use. Dispose of sharps and unused material per local regulations and institutional guidelines.
Who should not receive this treatment in a clinic setting?
Avoid use in individuals with known hypersensitivity to botulinum toxin components, those with active infection at intended injection sites, or patients with significant neuromuscular disorders unless carefully evaluated by the supervising provider. Limit administration to trained, licensed injectors. Review the product label and institutional criteria for eligibility, including current medications, prior history with neuromodulators, and risk factors relevant to your practice.
What onset and duration should teams anticipate?
Onset and duration vary by individual and injection parameters. Many clinics plan follow-up windows based on typical neuromodulator scheduling for type A toxins, which can support predictable appointment spacing. Avoid definitive claims and counsel conservatively. Photographs and standardized scales can help track changes over time. Coordinate patient check-ins based on your practice’s norms rather than fixed promises.
Can it be combined with fillers, devices, or skin boosters?
Yes, many clinics integrate neuromodulators with dermal fillers, energy-based devices, and topical programs. Space treatments according to your protocols and ensure informed consent reflects the plan. Consider staging to reduce confounding effects during assessment. Coordinate pre- and post-care guidance across modalities so patients receive clear, consistent instructions from all providers involved.
What post-injection guidance is typical after sessions?
Common guidance includes avoiding strenuous exercise, high-heat exposure, and massaging or manipulating treated areas for the first 24 hours. Transient effects like mild swelling, redness, or bruising can occur and generally resolve without intervention. Provide contact details for concerns and schedule follow-up per your practice norms. Document counseling, especially for first-time recipients, to standardize expectations and ensure continuity of care.
How are lot, expiry, and substitutions managed for inventory control?
Each vial’s label displays lot and expiration to support inventory logging and rotation. Align order cadence with your schedule and keep safety stock when feasible. If supply is constrained, review alternatives within the toxin class that fit your practice protocols. Update injector preferences, reconstitution steps, and consent language before substitution to maintain consistency across rooms and minimize variability.

Specifications

Main Ingredient: Botulinum Toxin A
Manufacturer: Hugel, Inc.
Drug Class:
Generic Name: Botulinum toxin type A
Package Contents: 100 U | 200 U
Storage Requirements: Refrigerated between 2°C – 8°C
Main Usage:

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