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Vitaran PN 1ml×2

$69.00

Quantity discounts
Quantity Discount Price
5-9 3% $66.93
10-19 5% $65.55
20-Unlimited 8% $63.48
SKU: FF-VITR-1ML-V2 Categories: ,
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Vitaran PN 1ml×2

Polynucleotide (Full Face) · PN 2% (20 mg/mL)
Quick Answer
Vitaran PN is the full-face counterpart to Vitaran i, delivering the same 20 mg/mL polynucleotide concentration from purified salmon trout DNA in two 1 mL syringes. It is positioned for whole-face biorevitalization — improving dermal density, elasticity, and skin tone through fibroblast activation. The standard course is 3–4 sessions spaced 2–3 weeks apart.
Last Reviewed
May 19, 2026
Manufacturer specification cross-verified
Treatment Protocol
3–4 sessions, 2–3 weeks apart. Maintenance every 4–6 months.

Why This Skinbooster Is Different

Vitaran PN extends LG Chem's HP Cell platform to whole-face indications. Compared to Vitaran i (periocular), it shares the same 20 mg/mL active but is positioned for larger anatomic fields. Compared to PDRN boosters like Lapuroon Aurora, Vitaran's PN uses longer-chain polynucleotides (purified by ultrafiltration to 500–5000 bp) which engage fibroblast receptors more efficiently than the shorter PDRN fragments.

Mechanism of Action

Polynucleotide Fibroblast Activator (full-face). PN fragments (250–800 kDa) activate fibroblast migration and proliferation through DNA-derived nucleotide signalling. Over a 3-session course, dermal density and skin quality improve cumulatively — measured outcomes include reduced surface roughness, decreased pore volume, increased dermal density.

Specifications

Product Name Vitaran PN 1ml×2
Category Polynucleotide (Full Face)
Active Ingredients 20 mg/mL polynucleotide sodium (PN 2%) extracted from purified salmon trout DNA + isotonic saline + buffer salts
Mechanism Class Polynucleotide Fibroblast Activator (full-face)
Manufacturer HP Cell Vitaran (LG Chem Life Sciences)
Origin Republic of Korea
Pack 2 × 1 mL pre-filled syringes
Lidocaine Not included
Injection Technique Nappage mesotherapy across the dermal field; or linear threading along static rhytids
Injection Depth Superficial to mid-dermis (1.5–3 mm)
Recommended Needle 30G or 31G recommended for full-face mesotherapy
Treatment Protocol 3–4 sessions, 2–3 weeks apart. Maintenance every 4–6 months.
Effect Duration 4–6 months after the initial course
Storage 2–25 °C, protect from light, do not freeze
Shelf Life 36 months unopened
Regulatory CE-marked Class III medical device. Manufactured under KGMP. Endotoxin tested <0.25 EU/mL.
SKU FF-SB-VITARAN-PN-1ML2

Clinical Indications

  • Full-face skin quality and dermal density
  • Cheek and temple skin elasticity
  • Neck and décolletage rejuvenation
  • Acne scarring and post-inflammatory dyschromia
  • Sun-damaged and photoaged skin

Compare Within Skinbooster Category

Product Active(s) Mechanism Protocol Duration
Vitaran PN 1ml×2 PN 2% (20 mg/mL) Polynucleotide Fibroblast Activator (full-face) 3–4 sessions, 2–3 weeks apart. Maintenance every 4–6 months. 4–6 months after the initial course
Rejuran HB Hydro Booster PN + HA + lidocaine PN + HA Hybrid with Premixed Lidocaine (Hydro Booster) 3 sessions, 3–4 weeks apart. Maintenance every 4–6 months. 4–6 months sustained skin quality and hydration improvement

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Frequently Asked Questions

What is Vitaran PN 1ml×2?
Vitaran PN is a full-face polynucleotide skinbooster containing 20 mg/mL (2%) purified salmon-trout PN in two 1 mL syringes. It improves dermal density, elasticity, and skin tone via fibroblast activation, and is delivered via mesotherapy or linear threading.
How does Vitaran PN differ from Vitaran i PN?
Same active ingredient at the same concentration — both are 20 mg/mL PN. Difference is positioning: Vitaran i is optimised for periocular treatment (1 mL syringes for the small bilateral field), while Vitaran PN is positioned for full-face biorevitalization at the same syringe volume.
How is Vitaran PN different from PDRN-based boosters like Lapuroon Aurora?
PDRN (polydeoxyribonucleotide) and PN (polynucleotide) are both salmon-DNA-derived but differ in chain length and purity. PN uses longer fragments (500–5000 bp) that engage fibroblast A2A receptors more efficiently. PDRN products typically also include HA, peptides, and vitamins as a cocktail; PN products are purer single-active formulations.
How is Vitaran PN compared to DIVA FACE PN?
Both are 2% PN full-face boosters from Korean manufacturers. Vitaran PN uses salmon trout DNA via the HP Cell platform; DIVA FACE PN by Lexyal uses salmon PN with 250-800 kDa molecular weight optimisation. Clinical performance is similar; brand preference and supply chain typically drive selection.
How many sessions are needed?
Standard protocol is 3 to 4 sessions, 2 to 3 weeks apart. Visible improvement in skin density and tone typically appears 2 to 4 weeks after each session and accumulates across the course. Maintenance is every 4 to 6 months.
What is the typical full-face dose per session?
A single full-face mesotherapy session typically uses 2 mL — which is exactly one 2-syringe Vitaran PN pack. Higher-density patients (severe photoaging, deeper rhytids) may use both syringes in 1 session, while milder cases split the pack across 2 visits.
Can Vitaran PN be combined with HA fillers?
Yes — Vitaran PN improves skin quality and dermal density while HA fillers add structural volume. Common protocols apply PN first to prime the dermis, then HA fillers 2 weeks later for volume. Not injected into the same field at the same session to avoid mixing in vivo.
Where is Vitaran PN manufactured?
Manufactured in Korea under the HP Cell Vitaran line by LG Chem Life Sciences. CE-marked Class III medical device with KGMP and ISO 13485 quality certification.
How should Vitaran PN be stored?
Store between 2 and 25 °C, protected from light and freezing. Shelf life is 36 months from manufacture. Each syringe is single-use sterile.
How much does Vitaran PN 1ml×2 cost?
Vitaran PN 1ml×2 is priced at USD $65.80 per 2-syringe box on Fillersfairy, with wholesale pricing for licensed practitioners.
Regulatory Notice. CE-marked Class III medical device. Manufactured under KGMP. Endotoxin tested <0.25 EU/mL. This product is manufactured outside the United States; FDA approval status is product-specific. For licensed healthcare professionals only. Practitioners are responsible for verifying regulatory status of this product in their jurisdiction before clinical use. Not for retail sale. Pricing subject to change.

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