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Liporase® Hyaluronidase Injection for Clinics
$132.99
Description
What Liporase Is and How It Works
Liporase® is a hyaluronidase preparation for injection used by trained clinicians to depolymerize hyaluronic acid fillers for controlled correction. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors. Our catalog supports US distribution to streamline procurement and scheduling for your team. This enzymatic agent acts on the glycosidic bonds of hyaluronic acid, allowing previously placed gels to be dispersed or removed with precision. Many practices rely on Hyaluronidase 1500 U when refining aesthetic outcomes or managing workflow contingencies across Dermal Filler Removal protocols.
The molecule facilitates diffusion of hyaluronic acid through selective cleavage, aiding redistribution or breakdown of gel deposits in the dermis and subcutaneous layers. Its role is procedural and supportive, helping teams correct asymmetry, reduce surface irregularities, or prepare an area before subsequent aesthetic steps. The product is intended for administration by credentialed professionals who follow internal guidelines, supervision, and post-procedure observation standards.
Professional Applications
In clinic practice, the product supports rapid adjustment of contour irregularities after hyaluronic acid filler placement. Teams also integrate it into emergency pathways for suspected intravascular events, in accordance with internal training and supervision. It can facilitate dissolving nodules, treating overcorrection, or preparing an area ahead of a subsequent filler session. When documented as Liporase hyaluronidase 1500 U, the vial serves as a familiar reference in procedure checklists. For additional context on safe technique, review Injection Protocols and explore Filler Removal Options.
Clinics may include this enzyme in standard aesthetic carts and emergency kits, aligning staff training with incident-response algorithms. It also supports cases where residual filler may interfere with other planned procedures, enabling a cleaner foundation for subsequent work. Your team can integrate the vial into quality and safety procedures that define consent, documentation, and follow-up schedules.
Key Features
- Clinical-use enzyme: supports HA gel dispersion.
- Defined strength: Liporase 1500 U vial for standardized preparation.
- Purified composition: bovine-derived hyaluronidase.
- Sterile packaging: glass vial in sealed blister.
- Flexible integration: fits aesthetic corrective workflows.
- Professional grade: prepared for medical environments.
- Clear labeling: lot and expiry on pack.
- Inventory friendly: compact unit for kits.
Benefits in Practice
Having hyaluronidase on hand can reduce rescheduling after unplanned filler outcomes. The preparation supports measured dissolution, helping teams meet patient expectations while adhering to clinic protocols. Triage, photography, and documentation integrate easily when a consistent formulation is used across rooms and providers.
Because hyaluronidase injection 1500 U is familiar across aesthetic training, staff can follow established steps with minimal disruption to queues. The product’s handling profile fits stocked emergency kits and routine aesthetic rooms. Its standardized composition supports predictable preparation, labeling, and hand-off between injectors and assistants.
Facilities also value the ability to align this item with broader categories such as Mesotherapy, where planning and post-care often intersect with filler management. Embedding the vial in your workflow can help unify protocols across service lines.
Composition & Ingredients
The active component is hyaluronidase, purified from bovine tissue and sterilized for injectable use. It enzymatically cleaves hyaluronic acid polymer chains, enabling controlled dispersion of HA-based gels. No excipient list is provided here; consult the pack insert for full information. For reference alignment, many clinicians document Hyaluronidase 1500 IU when describing unit content and inventory controls. Facilities may incorporate a hypersensitivity review into intake steps when bovine-derived products are used in practice.
Packaging & Supply
This product is supplied as a sterile glass vial secured within a sealed blister pack to protect integrity until use. Each unit includes clear labeling for lot number and expiration to support receiving checks and documentation. The presentation is intended for immediate preparation and administration by licensed injectors. Clinics use Liporase 1500 U as a standard-strength reference across aesthetic rooms and crash kits. For adjacent serums used in post-dissolution care, review NCTF 135 HA. Internal product code (SKU): 89585.
Packaging is designed to support clean handling, with components arranged to minimize touchpoints during setup. Always verify integrity of the blister and vial prior to use, and record lot and expiry according to your facility’s policy. The pack format is suitable for stocking in standardized trays, helping maintain consistent room readiness.
Ordering & Logistics
Licensed accounts can sign in to view contract and volume tiers, confirm allocations, and place orders. New customers undergo credential verification prior to fulfillment. When ordering Liporase (Hyaluronidase) 1500 U, your dashboard shows live availability and lead times. We support temperature-controlled handling when required and tracked US delivery. For broader therapy planning and inventory categories, see Mesotherapy and Pharmaceuticals.
Invoices, packing slips, and shipment confirmations are available for download from your account. Your team can request documentation as needed for internal receiving and QC processes. Lead times may vary by location and carrier service level.
Comparable Products
Clinics seeking parallel options can review Hynidase 1500IU or the multi-vial presentation Hyaluronidase 1500 UI for similar applications. Reviewing comparable items can help align preferences across injector teams while maintaining formulary flexibility.
Pricing & Access
Pricing is available to verified healthcare entities. Sign in to see tiered rates for multi-unit orders and potential contract terms aligned with your usage. Quotations can be generated from your account for purchasing review. Include item details on purchase requests to speed approval workflows.
Availability & Substitutions
Supply can vary by lot and importer. If your preferred configuration is on hold, our team can recommend a therapeutically comparable product after confirming clinical requirements and brand restrictions. We do not guarantee restock dates for discontinued or constrained items. Final product selection should reflect your medical director’s protocols and staff training.
Authoritative Sources
Sign in to reserve stock for your protocols and align shipment windows with procedure schedules.
Frequently Asked Questions
What is the role of this product in aesthetic workflows?
It serves as an enzymatic adjunct for managing hyaluronic acid filler corrections in professional settings. Clinics use it to disperse or remove previously placed HA gels when addressing asymmetry, contour irregularities, or overcorrection. It may also be included in complication protocols under appropriate supervision. Utilization should follow your internal procedures for consent, documentation, and follow-up, and be limited to staff trained in injectable therapies and aesthetic emergency response pathways.
How does hyaluronidase act on hyaluronic acid fillers?
Hyaluronidase cleaves specific bonds in hyaluronic acid polymers, enabling gels to redistribute or break down. This supports controlled correction when a filler adjustment is indicated. The effect depends on factors such as filler crosslinking, location, and time since placement, as well as technique and volume used. Because outcomes can vary, clinics typically standardize staff training, photo documentation, and observation protocols before and after administration.
What adverse reactions should clinicians monitor?
Common local reactions include redness, swelling, tenderness, and bruising at the injection site. Hypersensitivity, including allergic responses, is uncommon but possible, particularly with bovine-derived preparations. Tissue changes can occur if product is misapplied or used in inappropriate locations. Teams typically implement screening, careful technique, and post-procedure observation, with escalation pathways in place for unusual or severe responses noted during monitoring.
Are there preparation or dosing instructions available here?
This page does not provide dosing, dilution, or administration instructions. Facilities should follow the package insert, medical director guidance, and established training for injectable enzymes. Many clinics use competency checklists and stepwise procedures to maintain consistency. Documentation often includes product name, lot, expiry, anatomical site, and observation notes as part of the medical record and quality processes.
How is inventory typically stored and handled?
Follow the product label for storage conditions and expiration dating. Keep vials in their protective packaging until use, and inspect the blister and vial for integrity. Record lot and expiry during receiving and prior to administration. Clinics commonly place vials in standardized kits or trays for aesthetic rooms and emergency response carts, ensuring that trained staff can access the product quickly when indicated by protocol.
Does hyaluronidase work on all dermal fillers?
Hyaluronidase targets hyaluronic acid-based fillers. It does not dissolve non-hyaluronic acid products such as calcium hydroxylapatite or poly-L-lactic acid. When managing mixed-treatment histories, teams usually review prior records, examine the area, and consider imaging or staged approaches. The decision to proceed should align with the supervising clinician’s assessment and the facility’s safety and documentation standards.
What packaging details support quality control at receiving?
Units are supplied in a sterile glass vial within a sealed blister pack, with clear labeling for lot and expiration. These features support visual inspection, traceability, and documentation. Many clinics log each vial into inventory systems upon receipt, then record the same identifiers at administration. Single-use handling reduces cross-contamination risk and helps keep room setups consistent across providers and procedure types.
Specifications
- Main Ingredient: Hyaluronidase
- Manufacturer: Medytox Inc.
- Drug Class: Enzyme
- Generic Name: Hyaluronidase
- Package Contents: 5 mL x 10 Vials
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage:
About the Brand
Liporase
Here to help
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