Hyaluronidase 1500 IU Vials for Clinics
$87.99
Description
This lyophilized hyaluronidase preparation is supplied for reconstitution and injection in licensed clinical settings. It supports aesthetic workflows and tissue-permeability protocols where controlled enzymatic dispersion is required. Clinics value dependable potency, standardized handling, and US distribution.
What Hyaluronidase Is and How It Works
Hyaluronidase is an enzyme that hydrolyzes hyaluronic acid, reducing viscosity and improving tissue permeability. In practice, it can facilitate the dispersion of infused solutions and support aesthetic correction protocols under clinician direction. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.
This listing provides Hyaluronidase 1500 IU powder for injection in sterile, single-use vials. The lyophilized format helps maintain stability until reconstitution. Per facility protocol, reconstitute with sterile water only and do not co-mix with other products in the same syringe. The preparation integrates into clinic SOPs that require predictable onset and controlled handling.
Professional Applications
Clinics use this enzyme within aesthetic and procedural workflows where tissue permeability and dispersion control matter. Typical settings include hyaluronic-acid filler management, mesotherapy protocols, and infusion facilitation when a spreader enzyme is appropriate. When indicated, clinicians may deploy Hyaluronidase 1500 IU for filler dissolution during correction or harmonization visits, following local guidance and training.
For guidance on structured correction pathways, see our in-depth resources: Filler Correction Guide and Dermal Filler Options. For broader category planning and product selection, explore Dermal Filler Removal and Mesotherapy.
Key Features
- Lyophilized stability: Hyaluronidase 1500 IU lyophilized for dependable shelf readiness before reconstitution.
- Clinic-ready form: Sterile, single-use vials suited for controlled reconstitution and administration workflows.
- Consistent handling: Clear reconstitution step with sterile water only; do not co-mix with other products.
- Quality components: Manufactured with pharmaceutical-grade excipients to support reliable performance.
- Traceable inventory: Lot and expiration printed for intake checks and inventory control.
- Versatile integration: Fits aesthetic correction, dispersion assistance, and protocol-driven procedures.
- Regimen alignment: Works within established SOPs for filler correction and fluid dispersion.
- Portfolio fit: Complements a broad range of Pharmaceuticals stocked for procedure days.
Benefits in Practice
- Streamlined workflows: Predictable mixing and handling steps simplify staff training and turnover coverage.
- Protocol consistency: Standardized reconstitution supports reproducible results across providers and sites.
- Inventory control: Boxed vials help match appointment volume with on-hand supply planning.
- Flexible scheduling: Ready-to-prepare format supports same-day correction or planned touchpoints.
- Cross-team clarity: Common enzyme class eases cross-coverage between aesthetic and nursing teams.
- Kit compatibility: Many clinics organize a Hyaluronidase 1500 IU vial kit for immediate access during correction sessions.
Composition & Ingredients
Each vial contains lyophilized enzyme with supporting excipients. The formulation is designed for consistent dissolution in sterile water and controlled use in clinical environments.
- Active: Hyaluronidase (enzyme)
- Excipients: Mannitol, Sodium Phosphate, EDTA
Reported adverse events, while uncommon, may include allergic reactions such as rash, itching, or periocular swelling. Injection-site soreness, bleeding, or bruising can occur. Local swelling may be seen when used with subcutaneous infusions. Evaluate hypersensitivity risks and follow institutional protocols for test dosing or observation as required. Avoid co-mixing with other products in the same syringe; sequence products per clinic policy.
For procedural risk reduction and team alignment, review techniques highlighted in Injection Safety.
Packaging & Supply
The product ships as a box of five sterile vials. Each vial contains 0.508 mg of lyophilized enzyme. Labeling displays lot number and expiration date for intake documentation and rotation.
This presentation comprises Hyaluronidase 1500 IU injection vials intended for reconstitution with sterile water only. Do not mix with other products in the same syringe. Facility SOPs should specify reconstitution steps, solution handling, and labeling prior to administration. Packaging supports organized storage and quick retrieval in procedure rooms.
Ordering & Logistics
Account verification is required for licensed clinics and healthcare facilities. Sign in to view contract tiers and submit purchase requests. Your team can align delivery windows with procedure schedules and adjust quantities to match upcoming clinics.
We support formulary planning and replenishment across single-site and multi-site operations. For high-utilization settings, volume tiers are available on request. This product is positioned for Hyaluronidase 1500 IU wholesale acquisition within professional procurement workflows.
Comparable Products
Clinics that standardize on this enzyme class often evaluate related options for protocol alignment or formulary backup. Consider these alternatives from our catalog:
- LIPORASE Hyaluronidase for comparable enzyme utility.
- Hynidase 1500IU for an alternative presentation and sourcing pathway.
Pricing & Access
Sign in to your account to view current packs and pricing. Volume and contract tiers are available for qualifying facilities based on purchasing cadence and projected usage. Your representative can help align quantities with training sessions, new service launches, and seasonal demand.
Availability & Substitutions
Supply can vary based on market conditions and regulatory factors. If your preferred presentation is temporarily unavailable, our team can suggest clinically comparable listings. Confirm protocol compatibility and labeling before substitution. For broader options in this enzyme class and related protocols, review Dermal Filler Removal and Mesotherapy.
Authoritative Sources
- FDA: Hyaluronidase Injection Labeling
- NIH MedlinePlus: Hyaluronidase Injection
- NCBI Bookshelf: Hyaluronidase Overview
Ready to proceed? Sign in to confirm eligibility, view current stock, and schedule supply with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
What is included in the pack?
Each box contains five sterile, single-use vials of lyophilized enzyme. The vial content corresponds to a 1500‑IU presentation, labeled with lot and expiration for intake and rotation. This format supports controlled reconstitution with sterile water under clinic SOPs. Packaging is designed for quick retrieval and standardized storage in procedure rooms, helping teams prepare correction kits or protocol trays in advance of scheduled patients.
How should clinics reconstitute this product?
Follow your facility’s protocol and applicable guidance. This preparation is intended to be reconstituted with sterile water only, and it should not be co-mixed with other products in the same syringe. Use aseptic technique, label the solution clearly, and handle per your institution’s timeline for use. Do not interpret this as dosing guidance; defer to local policy, product labeling, and practitioner training for final instructions.
Which clinical workflows commonly use hyaluronidase?
Hyaluronidase integrates into aesthetic correction and harmonization visits involving hyaluronic‑acid fillers, mesotherapy protocols that call for dispersion assistance, and certain infusion workflows where tissue permeability is important. It may be included in correction kits for prompt response to filler concerns. Selection and use should align with clinician training, institutional guidelines, and the specific product labeling for your setting.
Can this be combined with other injectables?
Do not co‑mix with other products in the same syringe. If your protocol sequences multiple agents, administer them according to facility policy and product labeling. Consider compatibility, order of operations, and observation procedures. When addressing hyaluronic‑acid filler concerns, clinicians typically plan separate steps for enzyme administration and subsequent measures as needed, following accepted practice standards.
What adverse reactions should clinicians monitor?
Allergic reactions are uncommon but have been reported, including rash, itching, or swelling around the eyes. Injection‑site soreness, bleeding, or bruising can occur. Local swelling may be observed when used with subcutaneous infusions. Review patient history for hypersensitivity, consider test protocols where appropriate, and monitor post‑procedure according to your clinic’s observation guidelines.
How is quality and sterility maintained?
The product is supplied as sterile, lyophilized vials that are sealed until reconstitution. Packaging displays lot and expiration for intake checks. Use aseptic technique for dilution, label prepared solutions clearly, and discard per policy if beyond-use times are reached. Store and handle according to labeling and facility standards to maintain quality and support consistent performance across providers.
Do you offer related alternatives if this item is unavailable?
Yes. If supply fluctuates, our catalog includes comparable hyaluronidase options suitable for similar workflows. Examples include LIPORASE hyaluronidase and Hynidase presentations. Review our Dermal Filler Removal category for additional choices and confirm compatibility with your clinic’s protocols before substitution.
Specifications
- Main Ingredient: Manitiol, Sodium Phosphate, Edta
- Manufacturer: BCN
- Drug Class:
- Generic Name: Manitiol, Sodium Phosphate, Edta, Sodium Phosphate
- Package Contents: 5 mL x 5 Vials
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage:
About the Brand
INSTITUTE BCN
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