Where does this filler fit within a clinic’s portfolio?

This HA-based preparation is suited for facial soft tissue augmentation workflows overseen by trained injectors. Clinics commonly apply it to moderate-to-pronounced nasolabial folds, with selective use in marionette lines and midface contouring as allowed by internal protocols. Teams integrate it alongside other HA platforms to fine-tune lift, spread, and cohesivity by region. Selection should consider patient-specific anatomy, tissue quality, and the clinic’s preferred injection techniques and aftercare processes.

What is the role of polynucleotide sodium in this product?

Polynucleotide sodium is included to support dermal quality alongside the HA gel. It may promote a favorable environment for skin health through hydration balance and regenerative signaling. This mechanism complements the volumizing function of hyaluronic acid. While not a standalone skin booster, the component can be valuable in an HA matrix, helping clinics pursue aesthetic goals within comprehensive treatment plans determined by the prescriber.

What is the syringe format and needle compatibility?

The product is supplied as a sterile, prefilled 1 mL syringe. It is intended for professional use with standard injection sets familiar to licensed clinicians. Device selection, needle gauge, and technique should follow your clinic’s protocols, applicable regulations, and the product’s labeling. Do not reuse the syringe, and do not attempt to re-sterilize single-use components. Inspect packaging integrity and expiration before use.

How should it be stored prior to use?

Store according to the manufacturer’s label and any insert guidance. Protect from extremes of temperature and direct light during routine inventory handling. Maintain original packaging until time of use, and follow your clinic’s cold-room or controlled-room practices if applicable to the lot. Always verify the expiration date, inspect the seal, and document lot information in accordance with your internal procedures.

Can this filler be combined with other treatments in one visit?

Combination planning depends on the patient’s needs and your protocols. Some clinics stage energy-based devices or other injectables before or after HA treatments, allowing tissues to settle and minimizing confounding variables during assessment. When sequencing multiple modalities, evaluate timing, product interaction profiles, and aftercare to support safe outcomes. Follow your medical director’s guidance and local regulations when coordinating multi-modality sessions.

How is patient comfort addressed during administration?

The formulation includes an anesthetic to help reduce injection discomfort, which can streamline the procedure and may limit the need for additional topical numbing. Clinics still assess each patient’s tolerance and history, including sensitivities to anesthetic agents. Many providers pair vibration, cold packs, or other comfort measures as appropriate. Always follow your clinic’s consent, monitoring, and post-injection observation protocols.

What documentation is recommended for inventory and use?

Maintain records of product name, lot number, expiration date, and receipt date. Document the site of administration, amount used, and any adjunctive products applied per your charting standards. Record patient-specific considerations such as allergies, anesthetic sensitivities, and medical history as required. These basics support traceability, stock rotation, and quality assurance within a clinic’s broader materials management system.

Renefil Light Plus

Renefil Light Plus® Dermal Filler for Clinics

Name: Buy Renefil Light Plus® Dermal Filler – US Distribution
SKU: 100106
Price: 47.99 USD
Availability: InStock

Dermal Filler

$47.99

Description

What Renefil Light Plus® Is and How It Works

This injectable dermal filler is supplied as a sterile, prefilled 1 mL syringe for professional injection into facial soft tissue. The formulation pairs cross-linked hyaluronic acid with polynucleotide sodium and lidocaine hydrochloride to support volume restoration and comfortable administration. Clinics stock this preparation for consistent handling across midface, perioral, and fold-correction workflows. US distribution helps maintain predictable availability for scheduled sessions. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors.

Hyaluronic acid provides a viscoelastic gel matrix suitable for volumization and contouring. Polynucleotide sodium may support dermal quality through regenerative signaling and hydration balance. Lidocaine reduces injection discomfort, which can streamline chair time and tolerance. The material’s rheology allows precise placement by experienced injectors using standard aesthetic techniques.

Professional Applications

Clinics use Renefil Light Plus for targeted correction of moderate to pronounced nasolabial folds. Practices also deploy this filler for marionette lines and select midface contouring based on internal protocols. It can complement HA-based sculpting plans and staged rejuvenation programs. Explore broader categories such as Dermal Fillers and Skin Boosters to coordinate inventory and technique selection across patient cohorts.

For scenarios requiring greater projection or lift, many teams evaluate adjacent options in the same class. One example is Deep Plus Filler, which may be considered when firmer support is desired under clinical judgment.

Key Features

Cross-linked HA gel: stable matrix that supports localized structural lift.
Polynucleotide component: may aid tissue quality and elasticity maintenance.
Lidocaine inclusion: helps improve injection comfort during administration.
Prefilled syringe: sterile, single-use 1 mL configuration for predictable sessions.
Controlled extrusion: smooth flow that supports precise placement by trained injectors.
Balanced rheology: workable gel for shaping and contour refinement.
Clear labeling: lot and expiry printed for receiving and chart documentation.
Clinic fit: integrates with common HA filler workflows and device sets.

Benefits in Practice

This product fits cleanly into standard filler workflows. Smooth extrusion can enhance control during linear threading or small, localized deposits, depending on your technique. The integrated anesthetic may reduce the need for topical numbing, simplifying setup. Single 1 mL presentation supports predictable session planning and helps reduce partial-vial waste.

Handling characteristics align with expectations for established HA platforms, aiding quick onboarding for staff already familiar with comparable options such as Restylane 1 mL. Inventory teams benefit from clear labeling that supports lot tracking and rotation.

Composition & Ingredients

Renefil Light Plus contains:

Cross-linked hyaluronic acid (HA)
Polynucleotide sodium (PN)
Lidocaine hydrochloride 0.3% for local anesthetic effect

Ingredient ratios and inactive components follow manufacturer specifications. Refer to the carton and syringe label for the most current information.

Packaging & Supply

The product is provided as 1 mL x 1 syringe. Each unit is sterile and single-use, with lot number and expiration date visible on the labeling for rapid verification at receipt and prior to administration. The presence of lidocaine 0.3% is indicated on the package, supporting clinic-level checks for anesthetic sensitivities. Practices that routinely manage fold correction and midface contouring often pair this format with other HA options to tailor lift and spread characteristics across facial zones; for comparison, see Volume Plus Filler.

Packaging is designed for straightforward storage and bin placement. Carton dimensions and scannable identifiers support efficient receiving and cycle counts.

Ordering & Logistics

Available to verified, licensed accounts. Sign in to view contract and volume tiers aligned to your purchasing profile. Orders are processed through our professional B2B workflow for clinical buyers. Lead times can vary by demand and lot schedule. Please maintain an active license on file to avoid order delays.

Your team can coordinate replenishment cycles to align with appointment calendars and anticipated procedure volumes. If your practice uses multi-brand protocols, consider aligning delivery windows with other items in your filler and booster lines to streamline intake.

Comparable Products

Clinics seeking similar functionality within the HA category may also evaluate two established alternatives. For dynamic areas and tailored viscoelastic options, review the RHA Collection. For cohesive remodeling strategies, some teams assess Structura Filler alongside their existing HA portfolio, according to internal protocols.

Pricing & Access

Sign in to view Renefil Light Plus pricing aligned to your facility type. Qualified buyers can access volume and contract tiers based on committed purchasing. Quotes for multi-case plans are available to approved accounts. Final unit costs vary by lot availability, order size, and contractual terms.

Availability & Substitutions

Supply may vary by lot schedule and regional demand. If a preferred configuration is temporarily unavailable, your team can evaluate therapeutically appropriate substitutions from the same class in collaboration with the prescriber. For a structured overview of category choices, see our Filler Comparison resource.

Authoritative Sources

Ready to add this item to your formulary? Sign in to request supply with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

Where does this filler fit within a clinic’s portfolio?
This HA-based preparation is suited for facial soft tissue augmentation workflows overseen by trained injectors. Clinics commonly apply it to moderate-to-pronounced nasolabial folds, with selective use in marionette lines and midface contouring as allowed by internal protocols. Teams integrate it alongside other HA platforms to fine-tune lift, spread, and cohesivity by region. Selection should consider patient-specific anatomy, tissue quality, and the clinic’s preferred injection techniques and aftercare processes.
What is the role of polynucleotide sodium in this product?
Polynucleotide sodium is included to support dermal quality alongside the HA gel. It may promote a favorable environment for skin health through hydration balance and regenerative signaling. This mechanism complements the volumizing function of hyaluronic acid. While not a standalone skin booster, the component can be valuable in an HA matrix, helping clinics pursue aesthetic goals within comprehensive treatment plans determined by the prescriber.
What is the syringe format and needle compatibility?
The product is supplied as a sterile, prefilled 1 mL syringe. It is intended for professional use with standard injection sets familiar to licensed clinicians. Device selection, needle gauge, and technique should follow your clinic’s protocols, applicable regulations, and the product’s labeling. Do not reuse the syringe, and do not attempt to re-sterilize single-use components. Inspect packaging integrity and expiration before use.
How should it be stored prior to use?
Store according to the manufacturer’s label and any insert guidance. Protect from extremes of temperature and direct light during routine inventory handling. Maintain original packaging until time of use, and follow your clinic’s cold-room or controlled-room practices if applicable to the lot. Always verify the expiration date, inspect the seal, and document lot information in accordance with your internal procedures.
Can this filler be combined with other treatments in one visit?
Combination planning depends on the patient’s needs and your protocols. Some clinics stage energy-based devices or other injectables before or after HA treatments, allowing tissues to settle and minimizing confounding variables during assessment. When sequencing multiple modalities, evaluate timing, product interaction profiles, and aftercare to support safe outcomes. Follow your medical director’s guidance and local regulations when coordinating multi-modality sessions.
How is patient comfort addressed during administration?
The formulation includes an anesthetic to help reduce injection discomfort, which can streamline the procedure and may limit the need for additional topical numbing. Clinics still assess each patient’s tolerance and history, including sensitivities to anesthetic agents. Many providers pair vibration, cold packs, or other comfort measures as appropriate. Always follow your clinic’s consent, monitoring, and post-injection observation protocols.
What documentation is recommended for inventory and use?
Maintain records of product name, lot number, expiration date, and receipt date. Document the site of administration, amount used, and any adjunctive products applied per your charting standards. Record patient-specific considerations such as allergies, anesthetic sensitivities, and medical history as required. These basics support traceability, stock rotation, and quality assurance within a clinic’s broader materials management system.

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

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