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Lumi Face Polynucleotides Skin Booster

Lumi Face Polynucleotides Skin Booster

Dermaren

Skin Boosters
  • Marketed in the UK and EU by professional aesthetic wholesalers under the Dermaren brand as an injectable polynucleotide skin booster for trained practitioners.
  • Aesthetics Warehouse states that all of its products are CE or CPNP registered where required, but product Specific CE certificate numbers or MHRA device registrations for Lumi Face are not publicly detailed.
  • Dermaren Branded fillers and related products are manufactured by Across Co. Ltd., a South Korean company whose facilities are described as operating under recognised international quality and regulatory standards.
Polynucleotide Skin Booster

Description

Dermaren Lumi Face is an advanced, high-performance PN-based injectable skin booster developed with pharmaceutical-grade, ultra-purified polynucleotides (PN, 20mg/ml). Designed as a powerful alternative to Vitaran, it delivers deep hydration and promotes cellular regeneration to restore elasticity, smooth fine lines and wrinkles, and improve overall skin texture and radiance on the face, neck and décolletage. With its high concentration of PN, Lumi Face supports long-lasting improvements in tone, firmness and skin health, leaving the complexion brighter, smoother and more youthful.

Bnefits

  • High-concentration polynucleotides (20mg/ml) for effective skin regeneration and repair.
  • Deeply hydrates the skin and improves elasticity for a firmer, plumper appearance.
  • Reduces the appearance of fine lines and wrinkles by supporting collagen synthesis.
  • Enhances brightness and radiance, improving dull or tired-looking skin.
  • Promotes natural cell repair and regeneration for healthier, more resilient skin.
  • Suitable for full-face, neck and décolletage rejuvenation treatments.
  • Provides visible and long-lasting improvements in skin tone, texture and overall quality.

Indications

  • Photoaged or environmentally damaged skin requiring biorevitalisation.
  • Fine lines and superficial wrinkles on the face, neck and décolletage.
  • Loss of skin elasticity, firmness and density.
  • Dull, dehydrated or tired-looking skin that lacks radiance.
  • Uneven skin texture needing smoothing and refinement.
  • Supportive skin quality improvement in conjunction with other aesthetic procedures when clinically appropriate.

Composition

  • Polynucleotides (PN) 20mg/ml (ultra-purified pharmaceutical-grade polynucleotides).
  • Aqueous sterile injectable solution; no hyaluronic acid or lidocaine content is publicly listed for this product.
  • Exact excipient profile (buffers, salts, stabilisers) is not publicly disclosed; refer to official product literature for full ingredient list.

Formulation

  • PN-based injectable skin booster formulated with high-concentration, ultra-purified polynucleotides.
  • Biorevitalising, tissue-stimulating solution intended to support DNA repair, collagen and elastin synthesis and cellular regeneration.
  • Designed for intradermal or superficial subdermal administration by trained professionals using mesotherapy-style techniques.
  • Supplied as a sterile, ready-to-use solution for single-patient clinical use.

Packaging

  • Box containing 2 x 2ml pre-filled syringes of Dermaren Lumi Face.
  • Sterile, single-use syringes intended for professional injectable treatments.
  • Pack labelled for trained aesthetic and healthcare professionals only.
  • No additional accessories are guaranteed in all listings; some distributors may supply needles separately according to clinic needs.

Usage

  • For professional use only; treatment must be administered by suitably trained and qualified healthcare or aesthetic practitioners in accordance with local regulations.
  • Perform a full medical consultation and skin assessment to confirm indications, expectations and absence of contraindications before treatment.
  • Thoroughly cleanse and disinfect the treatment areas (face, neck, décolletage) before injection, ensuring all makeup and skincare residues are removed.
  • Use appropriate mesotherapy-style techniques (such as micro-bolus, nappage, or linear threading) to inject small amounts of product into the dermis or superficial subdermis, avoiding intravascular injection and respecting anatomical safety zones.
  • Dosage and injection pattern should be tailored to individual patient needs and clinic protocols; many distributors position Lumi Face for full-face or combined face/neck/décolletage rejuvenation using the supplied 2 x 2ml syringes over one or more sessions.
  • After injection, gently smooth or massage treated areas if clinically appropriate to aid even distribution and reduce papules or lumpiness, while monitoring patient comfort.
  • Provide detailed post-treatment advice, including avoiding makeup on treated areas for several hours, avoiding saunas, sunbeds, and intense exercise for 24–48 hours, and strict use of broad-spectrum sun protection.
  • Do not reuse opened syringes; discard any remaining product after a single treatment session according to local sharps and clinical waste protocols.
  • Always refer to the official instructions for use and manufacturer or distributor guidance for detailed administration techniques and recommendations.

Contraindications

  • Known hypersensitivity or allergy to polynucleotides or any component of the formulation.
  • Active skin infections, inflammatory skin diseases or open lesions at or near intended treatment sites.
  • Autoimmune diseases or immunosuppression where injectable aesthetic procedures are contraindicated, unless carefully evaluated by an appropriate specialist.
  • History of severe allergies, anaphylaxis or serious adverse reactions to injectable aesthetic treatments, unless assessed and performed with appropriate precautions.
  • Pregnancy and breastfeeding, as injectable aesthetic treatments are generally avoided due to limited safety data.
  • Uncontrolled systemic disease, significant coagulation disorders or concurrent anticoagulant therapy that substantially increases bleeding risk, unless managed in consultation with the patient’s physician.
  • Recent aggressive dermatologic procedures (e.g., deep chemical peels or ablative laser) in the proposed treatment area until adequate healing has occurred.
  • Any additional contraindications outlined in official product information or local clinical guidelines.

Adverse Effects

  • Common transient injection-site reactions such as redness, swelling, tenderness, mild pain, warmth or itching.
  • Small papules, nodules or unevenness at injection points, typically resolving as the product integrates into the tissue.
  • Bruising or haematoma formation in treated areas, particularly in more vascular regions.
  • Less common events such as prolonged oedema, local inflammation or induration, which may require clinical assessment and management.
  • Rare but serious complications associated with injectable treatments, including infection, abscess formation or vascular compromise and tissue necrosis if inadvertent intravascular injection occurs; these require urgent medical management according to local protocols.
  • Hypersensitivity or allergic reactions to product components; in very rare cases, severe reactions may require immediate medical intervention.

Storage Conditions

  • Store at a controlled temperature between 2 °C and 25 °C as specified by distributors.
  • Do not freeze; freezing may damage the product and compromise performance.
  • Keep syringes in their original packaging to protect from light and contamination until use.
  • Store in a secure, clean medical environment, out of reach of children and unauthorised persons.
  • Do not use after the expiry date printed on the packaging or if sterility appears compromised (e.g., damaged blister or syringe).

Duration

Distributors commonly report that treatment effects typically last between 6 and 12 months, depending on individual skin condition, lifestyle, and treatment protocol. Treatment courses often consist of multiple sessions scheduled several weeks apart, followed by periodic maintenance as determined by the treating practitioner.

Onset

Patients typically experience an increase in hydration and radiance in the weeks following treatment, with progressive improvements in elasticity, fine lines and overall texture as polynucleotides stimulate cellular regeneration and collagen production.

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