What clinical role does this filler serve?

This product is a cross-linked hyaluronic acid gel with polynucleotide sodium, designed for subcutaneous injection by trained professionals. Clinics use it to temporarily smooth moderate to severe facial folds and restore localized volume. It integrates well into facial rejuvenation protocols focused on contour support and fold softening. Selection and placement are based on anatomy, assessment, and provider technique. Review manufacturer materials and your practice guidelines before adding it to treatment plans.

How does the polynucleotide component contribute to performance?

Polynucleotide sodium is a hydrophilic polymer that can influence gel hydration and rheology. In combination with cross-linked hyaluronic acid, it supports a cohesive matrix designed for controlled extrusion and shape maintenance after placement. It is not a drug and does not replace clinical judgment about indication, plane, or volume. For full details, consult the official instructions for use and related scientific literature on polymer behavior in dermal fillers.

Where is this product typically placed within facial tissues?

The filler is intended for subcutaneous administration by trained injectors. Providers assess tissue thickness, mobility, and desired lift to determine precise placement technique. Avoid intravascular injection and follow standard safety practices, including aspiration protocols per clinic policy. Always refer to the manufacturer’s instructions for use and align with your facility’s procedural guidelines and training requirements.

How does lidocaine in the syringe affect workflow?

Integrated lidocaine can reduce the need for separate topical anesthetics and may enhance comfort during gel placement. This can shorten setup and help standardize patient experience between providers. Verify patient history for sensitivity to amide anesthetics and review contraindications. If lidocaine is unsuitable, follow your clinic’s alternative comfort measures and product selection protocols.

Can this filler be combined with other aesthetic injectables?

Many clinics coordinate dermal fillers with neuromodulators or skin boosters within broader programs. Sequencing and spacing depend on anatomy, product class, and provider preference. Use aseptic technique and avoid mixing products in the same syringe. Document all materials used, lot numbers, and treated areas. Tailor your plan to patient suitability and align with your practice’s safety policies and professional training.

What should clinics know about storage and handling?

Store and handle according to the manufacturer’s labeling. Keep the syringe in its original packaging until use, protect from extreme temperatures, and do not freeze. Use as a single-patient, single-use device and do not resterilize. Record the lot and expiry on procedure documentation. If there are any concerns about package integrity, quarantine the unit and contact support before use.

How can our team evaluate whether this product fits our formulary?

Assess anticipated indications, preferred gel viscosity, workflow compatibility, and staff familiarity with subcutaneous placement techniques. Compare this gel’s handling with other options your providers know well, and consider anesthesia preferences given the integrated lidocaine. Review available scientific resources, instructions for use, and internal outcomes data from trial appointments. If needed, schedule a small evaluation period to align ordering with upcoming procedure blocks.

Medical Devices

Renefil Ultra Plus

Renefil Ultra Plus® Injection for Clinics

Name: Renefil Ultra Plus® Injection – Professional Clinic Supply
SKU: 100104
Price: 47.99 USD
Availability: InStock

Dermal Filler

$47.99

Description

This injectable is a cross-linked hyaluronic acid and polynucleotide sodium dermal filler intended for subcutaneous administration in adults. It is used by trained clinicians to temporarily soften moderate to severe facial folds, including nasolabial lines, and to restore local volume. Practices stock it for consistent handling, predictable contouring, and flexible integration into aesthetic workflows. US distribution.

Renefil Ultra Plus® contains cross-linked sodium hyaluronate blended with polynucleotide sodium in a cohesive gel and includes lidocaine hydrochloride to support comfort during placement. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.

What Renefil Ultra Plus Is and How It Works

For licensed professionals, Renefil Ultra Plus injection is a hyaluronic acid-based dermal filler formulated for subcutaneous use. The cross-linking of sodium hyaluronate yields a viscoelastic gel that holds form under dynamic facial movement while allowing controlled extrusion through standard techniques. Polynucleotide sodium functions as a hydrophilic polymer that may enhance the gel’s rheology and tissue interface. Lidocaine is incorporated to reduce procedural discomfort during placement.

This product supports temporary restoration of soft-tissue contours, particularly in pronounced fold regions. The gel’s cohesion helps maintain localized lift and smooth transitions at the treatment site when deployed via standard aesthetic protocols. For a primer on ingredient behaviors in modern fillers, see Revofil Ingredients.

Professional Applications

Clinics use this preparation within comprehensive facial aesthetics programs. Typical applications include addressing moderate to severe nasolabial folds, marionette lines, and midface contour refinements where subcutaneous support is indicated. It can also complement cheek contouring or perioral rejuvenation plans when a cohesive gel with integrated anesthetic is preferred. Protocol placement is determined by clinician assessment, anatomy, and technique.

Many teams incorporate this filler alongside assessment tools, photography, and other consumables found under Medical Devices. Treatment planning often coordinates with practice guidelines for intake, post-procedure aftercare, and follow-up visits to support consistent outcomes across providers.

Key Features

Cross-linked HA gel: Provides structural support with controllable lift.
Polynucleotide component: Hydrophilic polymer that supports gel behavior.
Lidocaine included: Built-in local anesthetic for procedural comfort.
Subcutaneous placement: Designed for fold correction and contour support.
Consistent extrusion: Balanced viscosity for smooth expression.
Single-use syringe: Sterile, sealed, and ready for chairside use.
Clinic fit: Integrates with standard facial aesthetic workflows.
Quality focus: Professional-grade composition and traceable labeling.

Benefits in Practice

This product fits seamlessly into busy aesthetic schedules. The integrated lidocaine can streamline patient comfort measures and reduce the need for separate topical anesthetics. Consistent gel behavior supports steady injection feel, aiding precise placement across multiple facial landmarks. With a single-use, prefilled presentation, setup is straightforward and post-procedure handling is simplified.

From an operational standpoint, inventory is easy to manage due to standardized unit sizing. Documenting lot and expiry is direct from the outer carton and syringe label. Teams can align supply to appointment volumes, helping avoid overstock while maintaining readiness. For broader context on product selection across indications, see Wholesale Dermal Fillers.

Composition & Ingredients

Active components and anesthetic, as provided in manufacturer labeling:

Sodium polynucleotide
Cross-linked sodium hyaluronate
Lidocaine hydrochloride

Excipients and buffer systems follow manufacturer standards for sterile injectable gels. Refer to the unit carton and enclosed inserts for the full list of excipients and handling notes.

Packaging & Supply

The unit is supplied as a prefilled syringe for single-patient use. Pack configuration for this item: 1 ml x 1 syringe. Each carton and syringe carry batch and expiry identifiers to aid documentation and inventory tracking. Store and handle according to the label and instructions for use provided by the manufacturer.

Clinics often align ordering cycles to scheduled fold-correction appointments to coordinate chair time and staff allocation. When you evaluate inventory by procedure type, Renefil Ultra Plus can be grouped with other mid-viscosity HA fillers to streamline stocking practices. Internal product reference: SKU 100104.

Ordering & Logistics

Licensed account verification is required prior to fulfillment. Sign in to view contract tiers, request quotes, and place orders aligned to your clinic calendar. For operations teams planning regional distribution, information regarding Renefil Ultra Plus US shipping and lead times is available after account activation. Consolidate shipments when practical to reduce receiving touches and to maintain consistent availability between provider schedules.

Most clinics coordinate deliveries with procedure blocks and pre-appointment confirmations. Our team supports multi-site ordering, backorder guidance, and product substitutions when appropriate and approved by your practice.

Comparable Products

Clinics comparing gel behavior, viscosity, and presentation may also review adjacent options. Within the same family, see Renefil Light Plus for alternative handling characteristics. For clinics using hyaluronic acid fillers across multiple indication sets, consider Revanesse Ultra or the midface workhorse listed as Volume Filler 1 mL.

For a broader view of portfolio segmentation by indication and rheology, the article Stylage Guide can help frame selection discussions during formulary meetings.

Pricing & Access

Sign in to view Renefil Ultra Plus price, current promotions applicable to licensed practices, and volume or contract tiers. Multi-case quotations can be generated for planned campaigns or seasonal appointment surges. No pricing is displayed to the public; access is reserved for verified clinical buyers.

Availability & Substitutions

Supply can vary by manufacturer cycle and regional demand. If the requested unit is temporarily unavailable, our team can discuss clinically appropriate substitutes in the same class and viscosity range. Confirm any substitution against your protocols and patient population before updating treatment plans. We do not make restock guarantees; lead times are communicated at the time of order.

Authoritative Sources

Closing

Ready to stock this preparation for your aesthetic workflows? Sign in to confirm your clinic access, align quantities to your schedule, and order with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

What clinical role does this filler serve?
This product is a cross-linked hyaluronic acid gel with polynucleotide sodium, designed for subcutaneous injection by trained professionals. Clinics use it to temporarily smooth moderate to severe facial folds and restore localized volume. It integrates well into facial rejuvenation protocols focused on contour support and fold softening. Selection and placement are based on anatomy, assessment, and provider technique. Review manufacturer materials and your practice guidelines before adding it to treatment plans.
How does the polynucleotide component contribute to performance?
Polynucleotide sodium is a hydrophilic polymer that can influence gel hydration and rheology. In combination with cross-linked hyaluronic acid, it supports a cohesive matrix designed for controlled extrusion and shape maintenance after placement. It is not a drug and does not replace clinical judgment about indication, plane, or volume. For full details, consult the official instructions for use and related scientific literature on polymer behavior in dermal fillers.
Where is this product typically placed within facial tissues?
The filler is intended for subcutaneous administration by trained injectors. Providers assess tissue thickness, mobility, and desired lift to determine precise placement technique. Avoid intravascular injection and follow standard safety practices, including aspiration protocols per clinic policy. Always refer to the manufacturer’s instructions for use and align with your facility’s procedural guidelines and training requirements.
How does lidocaine in the syringe affect workflow?
Integrated lidocaine can reduce the need for separate topical anesthetics and may enhance comfort during gel placement. This can shorten setup and help standardize patient experience between providers. Verify patient history for sensitivity to amide anesthetics and review contraindications. If lidocaine is unsuitable, follow your clinic’s alternative comfort measures and product selection protocols.
Can this filler be combined with other aesthetic injectables?
Many clinics coordinate dermal fillers with neuromodulators or skin boosters within broader programs. Sequencing and spacing depend on anatomy, product class, and provider preference. Use aseptic technique and avoid mixing products in the same syringe. Document all materials used, lot numbers, and treated areas. Tailor your plan to patient suitability and align with your practice’s safety policies and professional training.
What should clinics know about storage and handling?
Store and handle according to the manufacturer’s labeling. Keep the syringe in its original packaging until use, protect from extreme temperatures, and do not freeze. Use as a single-patient, single-use device and do not resterilize. Record the lot and expiry on procedure documentation. If there are any concerns about package integrity, quarantine the unit and contact support before use.
How can our team evaluate whether this product fits our formulary?
Assess anticipated indications, preferred gel viscosity, workflow compatibility, and staff familiarity with subcutaneous placement techniques. Compare this gel’s handling with other options your providers know well, and consider anesthesia preferences given the integrated lidocaine. Review available scientific resources, instructions for use, and internal outcomes data from trial appointments. If needed, schedule a small evaluation period to align ordering with upcoming procedure blocks.

Specifications

Main Ingredient: Lidocaine Hydrochloride, Sodium Hyaluronate
Manufacturer: BMI KOREA
Drug Class: Dermal Filler
Generic Name: Sodium polynucleotide + cross-linked sodium hyaluronate + lidocaine hydrochloride
Package Contents: 1 ml x 1 Syringe
Storage Requirements: Room Temperature (2℃~25℃)
Main Usage: Volume Filler, Fine Lines

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