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Pure Pro PN Skin Booster

Pure Pro PN Skin Booster

Pure

Skin Booster
  • Described by UK distributors as a CE Approved injectable device/skin booster.
  • Manufactured in South Korea in facilities described by the manufacturer as compliant with US cGMP and EU GMP standards for medical Grade PN production.
Injectable polynucleotide (PN) skin booster

Description

Pure Pro PN Skin Booster is an advanced polynucleotide-based injectable skin booster that combines purified salmon DNA–derived polynucleotides (PN) with hyaluronic acid, peptides, and amino acids. It is designed for bio-revitalisation and anti-ageing of the skin, improving hydration, elasticity, texture, and overall skin quality. Supplied as a 2 ml pre-filled syringe, it is used with a micro-droplet injection technique to stimulate collagen and elastin production, reduce fine lines and wrinkles, refine pores, and restore radiance to dull, tired skin.

Bnefits

  • Skin rejuvenation and regeneration, improving texture and clarity
  • Deep hydration and restoration of skin moisture for a plumper appearance
  • Collagen and elastin stimulation to improve skin firmness and elasticity
  • Improvement in skin tone and pigmentation by increasing dermal thickness and density
  • Pore tightening by filling and refining enlarged pores from within
  • Enhanced skin repair and regeneration via polynucleotides from purified salmon DNA
  • Multi-area use: suitable for face, neck, hands, elbows and other ageing-prone areas
  • Quick visible effect typically within 3–5 days after the first procedure
  • Long-lasting results, with effects commonly maintained for around 6 months after a recommended course
  • Gradual, natural-looking results without the use of volumising filler substances

Indications

  • Mild to moderate skin laxity
  • Fine lines and early wrinkles
  • Dry or dehydrated skin
  • Dull, tired-looking skin lacking radiance
  • Irregular or rough skin texture
  • Enlarged pores
  • General signs of skin ageing on the face, neck, hands and other exposed areas

Composition

  • Polynucleotide (PN) – medical-grade polynucleotides extracted and purified from Alaskan salmon DNA
  • Hyaluronic acid – injectable HA gel to enhance hydration and support dermal structure
  • Peptides: Acetyl Hexapeptide-8 (neurotransmitter-inhibiting peptide supporting wrinkle reduction)
  • Peptides: Octapeptide-4 (helps protect skin from free radicals and oxidative stress)
  • Peptides: Palmitoyl Pentapeptide-4 (stimulates collagen, elastic fibres and hyaluronic acid, improving moisture and reducing fine lines)
  • Amino acids: Glycine
  • Amino acids: Proline
  • Amino acids: L-Hydroxyproline
  • Amino acids: Leucine
  • Amino acids: Glutamine
  • Amino acids: L-Lysine
  • Amino acids: Methionine

Formulation

  • Sterile injectable solution for intradermal use
  • Polynucleotide + hyaluronic acid + peptide + amino acid complex
  • Supplied in a pre-filled 2 ml syringe intended for micro-droplet injection technique

Packaging

  • Box containing 1 pre-filled syringe x 2 ml
  • No needles supplied with the syringe (needles/cannulas sourced separately)
  • Manufactured in South Korea

Usage

  • Professional use only – treatment should be performed by suitably trained and qualified medical or aesthetics practitioners following local regulations and the official instructions for use.
  • Method: micro-droplet technique into the dermis.
  • Recommended needle size: approximately 32G, 4 mm; cannula (optional): 22–23G, 50–70 mm (per manufacturer protocol).
  • Injection areas commonly treated include: forehead, crow’s feet, cheeks, neck, backs of the hands and elbows.
  • At approximately 1 cm intervals, inject 0.025–0.05 ml per point across the treatment area.
  • Inject a total of 2 ml (one full syringe) distributed evenly throughout the procedure area per session, according to clinical judgment.
  • Recommended treatment course: 3 sessions spaced 2–3 weeks apart.
  • Subsequent maintenance treatments may be scheduled according to individual patient response and practitioner assessment, typically after the 6-month effect period.
  • Before treatment, assess medical history, indications, contraindications and obtain informed consent; follow aseptic technique and post-treatment care instructions per manufacturer guidance.

Contraindications

  • Specific contraindications are not detailed in the publicly accessible marketing materials reviewed.
  • Practitioners should refer to the official instructions for use (IFU), product labelling and local clinical guidelines for full contraindication information (for example, conditions such as local infection, known hypersensitivity to components, or other standard injectable therapy exclusions).

Adverse Effects

  • No detailed adverse event profile is provided in the publicly available product brochures and distributor descriptions.
  • As with other injectable skin boosters, potential adverse effects may include transient injection-site reactions such as redness, swelling, bruising, tenderness, or small papules; practitioners should consult the official IFU and follow pharmacovigilance and reporting requirements.

Storage Conditions

  • Specific temperature and storage conditions are not clearly specified in the open marketing materials located.
  • Store and handle according to the instructions on the product packaging and official instructions for use, typically in a controlled environment away from extreme temperatures, light and contamination.

Duration

Typical protocol: 3 treatment sessions at 2\u20133 week intervals, with clinical effects lasting around 6 months after the course, according to manufacturer and distributor information.

Onset

Quick effect is usually reported 3\u20135 days after the first procedure, with progressive improvements over the following weeks as collagen regeneration is stimulated.

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