Description
This polynucleotide injectable is intended for professional administration to support visible skin quality. Clinics integrate it into texture refinement, tone management, and scar-focused protocols. Streamlined sourcing via US distribution helps standardize inventory planning across multi-site operations.
What Rejuran Is and How It Works
Rejuran® Healer is an injectable preparation containing highly purified polynucleotides derived from salmon DNA. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors. The formulation is used by trained clinicians to support dermal regeneration processes, promote extracellular matrix renewal, and strengthen barrier function. It is positioned for skin-quality improvement rather than volumization.
Within clinic workflows, the Rejuran Healer injection is selected to complement technique-driven aesthetic programs. The preparation’s biocompatible PN chains help create a favorable environment for fibroblast activity and collagen support. Many teams deploy it as part of periodic skin-maintenance schedules, or as an adjunct following device-based treatments, based on practitioner judgment and local regulations.
Professional Applications
Typical use cases include quality-focused facial rejuvenation programs, fine-line softening strategies, pore-appearance management, and post-procedure skin support. In multi-modality sessions, it can be combined with energy-based devices or micro-needling according to clinic protocols. Within skin-quality programming, some teams refer to it as a Rejuran skin booster when describing its role in dermal revitalization.
To compare classes and protocols, explore Skin Boosters or review adjunct options such as Sunekos. For thread-based lifting or structural refinement, see our PDO Threads Guide. This preparation also aligns with Mesotherapy protocols where permitted.
Key Features
- PN composition: purified polynucleotides sourced from salmon DNA
- Skin-quality focus: supports tissue environment and matrix renewal
- Professional use: injectable format for trained practitioners
- Non-volumizing role: complements fillers without replacing volume products
- Sterile presentation: produced under quality-led manufacturing standards
- Barrier support: helps reinforce hydration and epidermal resilience
- Label clarity: lot and expiration information for traceability
- Flexible integration: compatible with multi-modality aesthetic workflows
Benefits in Practice
This product integrates smoothly into existing aesthetic pathways. Its handling characteristics fit common micro-deposit techniques and device-assisted approaches determined by clinical preference. Teams often schedule it alongside other skin-quality boosters or as a maintenance element for texture and tone programs.
- Workflow fit: usable as stand-alone or adjunct within established pathways
- Consistent handling: predictable rheology supports controlled placement
- Protocol flexibility: adaptable across seasonal and maintenance plans
- Inventory simplicity: one line item supports multiple skin-quality aims
- Traceability: clear lot and expiry data streamline recordkeeping
- Tool compatibility: pairs with fine-gauge delivery options and micro-needling tools
For device-assisted microinjection, clinics often employ specialized tools; see MicronJet for potential workflow compatibility.
Composition & Ingredients
The polynucleotides in this preparation are engineered for biocompatibility and dermal support. In many references, the PN component is described as Rejuran PN within the broader skin-quality category. The solution is prepared in a sterile, isotonic carrier designed for injectable use in professional settings.
- Polynucleotides (PN), salmon DNA origin
- Water for injection
- Buffer salts and pH adjusters
Clinics comparing PN-based options may also evaluate Nucleofill 2.0 for class reference.
Packaging & Supply
Supplied as a sterile injectable preparation for professional use. Units include manufacturer labeling with lot number and expiration date for inventory control. Storage and handling should follow the manufacturer’s instructions on the carton and leaflet. Product identifiers and documentation facilitate integration into clinic procurement systems. Reference SKU: 89439.
Ordering & Logistics
Licensed account verification is required prior to fulfillment. Sign in to view volume and contract pricing options aligned with your purchasing policies. Orders are processed through established distribution channels with visibility into lead times when available. Packaging and transport practices follow medical supply standards, with handling protocols aligned to the product’s labeled requirements. Only trained, authorized professionals should administer this injectable in accordance with local regulations.
Comparable Products
Clinics seeking related formulations sometimes evaluate the periocular-focused variant, known as Rejuran Eye, when building area-specific protocols. For non-PN alternatives within the skin-quality category, consider Profhilo Structura or RRS HA Long-Lasting to compare composition and workflow role.
Pricing & Access
Sign in with a verified professional account to view pricing. Contract and tiered volume options are available for qualified facilities. Quotes can be aligned to clinic purchasing cycles and multi-site needs. No consumer sales are offered.
Availability & Substitutions
Supply can vary by lot and distribution timing. When inventory is constrained, clinics often confirm acceptable substitutes within the same treatment class before scheduling. Alternative products should be reviewed by the supervising practitioner to ensure protocol continuity and comparable workflow characteristics.
Authoritative Sources
Sign in to place an order and maintain continuity for skin-quality programs with temperature-controlled handling when required and tracked US delivery.
Frequently Asked Questions
What is the active technology?
This injectable contains highly purified polynucleotides (PN) derived from salmon DNA. PN are long-chain molecules that can support extracellular matrix dynamics and hydration balance in professional skin-quality programs. The preparation is non-volumizing and is selected for its role in dermal support rather than contouring. Composition specifics and excipients appear on the manufacturer’s labeling and accompanying leaflet. Always follow the latest product insert and local regulations when incorporating it into clinical protocols.
How is it used in clinic protocols?
Clinics position this preparation for texture refinement, fine-line softening, and tone-focused maintenance, often within multi-modality regimens. In some programs, teams describe it as a Rejuran Healer skin booster to reflect its role in skin-quality improvement. Scheduling, sequencing with devices, and session counts vary by practitioner judgment, patient presentation, and local guidance. It may be combined with energy-based systems or micro-needling when appropriate to the protocol.
Can it be combined with HA boosters?
Many clinics pair polynucleotide injectables with hyaluronic acid skin-quality products in alternating sessions or phased plans. This approach can support hydration and tissue environment benefits while maintaining a non-volumizing profile. Product selection, timing, and technique are determined by the supervising practitioner. Review manufacturer guidance and ensure compatibility across all planned modalities before creating a combined plan for a given case.
Which applicators are commonly selected?
Fine-gauge needles, micro-needling systems, and specialty microinjection devices are frequently used in skin-quality programs. Device selection depends on the target area, skin condition, and practitioner techniques. Clinics should confirm compatibility with the injectable’s labeled guidance and their internal protocols. Appropriate antisepsis, sterile disposables, and post-care instructions are part of standard professional practice and should follow local requirements.
How do clinics plan session intervals?
Intervals and total sessions vary by clinic preference, device pairing, and individual presentation. Some teams run a short induction phase followed by periodic maintenance, while others integrate sessions alongside energy-based treatments. The supervising practitioner defines the cadence, number of sessions, and any adjunctive measures in line with training, clinical objectives, and the product’s labeling. Avoid fixed schedules without professional assessment.
How do Eye and S variants differ?
The Eye version is often used for delicate periocular applications within skin-quality plans. By contrast, Rejuran S is typically discussed in the context of focal textural irregularities such as scar-prone areas. Selection depends on treatment goals, technique, and clinical judgment. Always confirm product indications, area suitability, and labeled guidance before choosing a variant for a specific protocol.
Who is authorized to administer it?
Administration is restricted to licensed healthcare professionals acting within their scope of practice. Credentialing, supervision requirements, and setting standards vary by state and facility policy. Only trained personnel should perform injections, use sterile technique, and manage post-procedure guidance. The product is not intended for home use, self-administration, or retail channels. Clinics should follow applicable regulations and manufacturer instructions.
Specifications
- Main Ingredient: Polynucleotides
- Manufacturer: Pharma Research Products
- Drug Class: Cosmetic Injectable
- Generic Name: Polynucleotides
- Package Contents: 2 mL x 2Pre-Filled Syringes
- Storage Requirements: Room Temperature (2℃~25℃)
- Main Usage: Volume Filler, Anti Ageing
About the Brand
Rejuran
Here to help
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