

Hyaron® Skin Booster – 10 × 2.5ml | Sodium Hyaluronate
Product Overview
Hyaron® is a professional non-cross-linked Sodium Hyaluronate skin booster developed to provide intensive skin hydration, biorevitalisation and overall improvement in skin quality.
Manufactured by Dongkook Pharmaceutical in South Korea, Hyaron® contains highly purified Sodium Hyaluronate produced through microbial fermentation and is designed for professional injectable skin-rejuvenation treatments.
Each 2.5ml pre-filled syringe contains 25mg of Sodium Hyaluronate, providing a lightweight, hydrating formulation designed to integrate within the skin without the structural volumising characteristics associated with cross-linked dermal fillers.
Unlike traditional cross-linked Hyaluronic Acid fillers, which are typically designed to create volume, projection or facial contour, Hyaron® focuses primarily on hydration and skin-quality improvement.
The non-cross-linked Sodium Hyaluronate helps replenish moisture within the skin and supports improvements in:
Skin hydration
Moisture retention
Skin elasticity
Skin smoothness
Dermal suppleness
Skin texture
Skin radiance
Overall skin quality
Its lightweight formulation makes Hyaron® particularly suited to professional mesotherapy and skin-rejuvenation protocols for patients experiencing dry, dehydrated or ageing skin.
Rather than changing facial structure, Hyaron® is intended to support healthier-looking, smoother and more hydrated skin while maintaining natural facial contours.
Hyaron® is intended strictly for use by appropriately qualified medical or aesthetic professionals trained in injectable skin-rejuvenation procedures.
Pack Contents
Each pack contains:
10 × 2.5ml pre-filled sterile syringes of Hyaron®
25mg Sodium Hyaluronate per syringe
Sterile professional-use packaging
Single-use syringes
Volume per Syringe: 2.5ml
Total Pack Volume: 25ml
Sodium Hyaluronate per Syringe: 25mg
Sodium Hyaluronate Concentration: 10mg/ml
Always check the individual product packaging, manufacturer labelling and current Instructions for Use before administration.
Product CompositionSodium Hyaluronate – 25mg / 2.5ml
The principal component of Hyaron® is non-cross-linked Sodium Hyaluronate.
Each 2.5ml syringe contains:
25mg Sodium Hyaluronate
Equivalent to:
10mg/ml Sodium Hyaluronate
Sodium Hyaluronate is the sodium salt of Hyaluronic Acid and is recognised for its ability to bind and retain water.
Within Hyaron®, the non-cross-linked Sodium Hyaluronate is designed primarily to support skin hydration and overall dermal quality rather than create structural facial volume.
It may support:
Improved skin hydration
Increased moisture retention
Improved skin elasticity
Improved skin smoothness
Enhanced dermal suppleness
Healthier-looking skin
Improved overall skin quality
Sodium Chloride
Sodium Chloride forms part of the formulation and helps maintain appropriate physiological osmolarity while contributing to product stability.
Monobasic Sodium Phosphate
Monobasic Sodium Phosphate forms part of the product's buffering system and helps maintain an appropriate pH and formulation stability.
Water for Injection
Sterile Water for Injection provides the carrier solution for the formulation.
Non-Cross-Linked Hyaluronic Acid Technology
One of the defining characteristics of Hyaron® is its use of non-cross-linked Sodium Hyaluronate.
Cross-linking is commonly used in structural Hyaluronic Acid dermal fillers to increase gel persistence and provide properties suitable for volume, projection and contouring.
Hyaron® takes a different approach.
Its non-cross-linked formulation is designed primarily to disperse within the treated tissue and support hydration rather than create substantial physical volume.
This makes the treatment more appropriate for skin-quality objectives such as:
Hydration
Smoothness
Elasticity
Suppleness
Texture
Radiance
The primary objective is therefore biorevitalisation and skin-quality improvement rather than facial augmentation.
Skin Hydration & Biorevitalisation
Hyaluronic Acid is naturally present within the skin and extracellular matrix, where it plays an important role in hydration and tissue homeostasis.
Its ability to attract and retain water contributes to the skin's:
Hydration
Elasticity
Suppleness
Smoothness
Overall appearance
Changes associated with ageing and environmental exposure can contribute to reduced hydration and deterioration in overall skin quality.
This may present as:
Dryness
Dehydration
Dull-looking skin
Reduced elasticity
Rougher texture
Reduced suppleness
Fine dehydration lines
Hyaron® is designed to replenish hydration within the skin using non-cross-linked Sodium Hyaluronate.
By supporting moisture levels within the treated tissue, Hyaron® may contribute to smoother, softer and more radiant-looking skin.
Moisture Retention
Sodium Hyaluronate has strong water-binding properties.
Following appropriate professional administration, the Sodium Hyaluronate within Hyaron® helps support moisture retention within the treated tissue.
Improved hydration may contribute to:
Softer-feeling skin
Smoother-looking texture
Improved elasticity
Greater suppleness
Improved radiance
Reduced appearance of dehydration-related fine lines
Healthier-looking skin
Because Hyaron® is non-cross-linked, the treatment should not be approached as a structural replacement for a conventional dermal filler.
Key Benefits
Professional non-cross-linked Sodium Hyaluronate skin booster
Manufactured by Dongkook Pharmaceutical
Manufactured in South Korea
10 × 2.5ml pre-filled syringes
25ml total pack volume
25mg Sodium Hyaluronate per syringe
Equivalent to 10mg/ml Sodium Hyaluronate
Designed for intensive skin hydration
Supports moisture retention
Helps improve skin elasticity
Supports smoother-looking skin
Helps improve skin texture
Supports dermal suppleness
Helps improve skin radiance
May reduce the appearance of dehydration-related fine lines
Designed for skin biorevitalisation
Suitable for professional mesotherapy protocols where indicated
Suitable for general skin-rejuvenation protocols
Non-cross-linked formulation
Does not primarily provide structural facial volume
Supports natural-looking skin rejuvenation
Intended strictly for appropriately qualified professional use
Common Treatment Areas
Following appropriate consultation and professional assessment, Hyaron® may be incorporated into skin-rejuvenation protocols involving:
Full face
Neck
Décolletage
Back of the hands
Perioral region
Forehead
Cheeks
Chin
Jawline
Areas demonstrating dry skin
Areas demonstrating dehydration
Areas demonstrating age-related deterioration in skin quality
Treatment area suitability should always be determined according to the patient's individual anatomy, skin condition, medical history and treatment objectives.
Always follow the manufacturer's current Instructions for Use regarding approved indications, administration technique, treatment depth, product volume and placement.
Hyaron® vs Cross-Linked Dermal Fillers
Hyaron® should not be considered equivalent to a conventional cross-linked Hyaluronic Acid dermal filler.
Cross-Linked HA Dermal Fillers
These products are generally designed to provide:
Physical volume
Projection
Structural support
Facial contouring
Correction of selected wrinkles and folds
Hyaron®
Hyaron® is designed primarily to support:
Skin hydration
Moisture retention
Skin elasticity
Dermal suppleness
Skin smoothness
Skin texture
Skin radiance
Overall skin quality
Its primary objective is therefore skin hydration and biorevitalisation rather than structural augmentation.
Hyaron® vs Polynucleotide Skin Boosters
Hyaron® also differs from Polynucleotide or PDRN-based regenerative skin boosters.
Hyaron®
The principal active component is:
Non-cross-linked Sodium Hyaluronate
Its primary treatment focus is:
Hydration
Moisture retention
Elasticity
Smoothness
Skin biorevitalisation
PN / PDRN Skin Boosters
Polynucleotide-based products are typically positioned around regenerative mechanisms such as:
Fibroblast support
Tissue regeneration
Extracellular matrix support
Collagen-related regenerative activity
Hyaron® therefore provides an option where the primary treatment objective is HA-based hydration and general skin revitalisation.
Recommended Treatment Course
Hyaron® should only be administered by practitioners appropriately trained in professional injectable skin-rejuvenation procedures.
A commonly referenced treatment approach described in the supplied product information is:
Initial Course: 3 treatment sessions
Treatment Interval: Approximately every 3–4 weeks
Maintenance: Approximately every 3–6 months, depending upon skin condition and clinical response
These intervals should not be considered a universal or mandatory protocol.
The appropriate treatment schedule should be individually determined according to:
Patient age
Baseline skin condition
Degree of dehydration
Skin elasticity
Treatment area
Medical history
Previous aesthetic procedures
Clinical response
Individual treatment objectives
The manufacturer's current Instructions for Use should always take precedence over commonly referenced treatment schedules.
Professional Treatment Considerations
Hyaron® is intended for administration by appropriately qualified and trained medical or aesthetic professionals with suitable knowledge of injectable skin-rejuvenation procedures.
Treatment planning should include:
Comprehensive medical consultation
Review of medical history
Assessment of skin quality
Assessment of hydration levels
Evaluation of the proposed treatment area
Review of previous aesthetic procedures
Assessment of contraindications
Discussion of realistic treatment expectations
Explanation of potential adverse effects and complications
Completion of appropriate documented informed consent
Injection technique, treatment depth, product volume and distribution should always be determined according to individual anatomy, skin condition, practitioner assessment and the manufacturer's current Instructions for Use.
Hyaron® should not be administered using a generic protocol without appropriate consideration of patient-specific factors.
Results & Treatment Outcomes
Hyaron® is designed primarily to support hydration and overall skin-quality improvement.
Patients may notice improvements in skin hydration and luminosity as moisture levels within the treated tissue increase.
Potential treatment outcomes may include:
Improved skin hydration
Improved moisture retention
Better skin elasticity
Smoother-looking skin
Improved skin texture
Increased suppleness
Improved radiance
Healthier-looking skin
Reduction in the appearance of dehydration-related fine lines
A professionally planned course of treatment may be used where progressive improvement in skin hydration and overall quality is desired.
As Hyaron® contains non-cross-linked Sodium Hyaluronate, maintenance treatment may subsequently be considered to support ongoing skin hydration.
Individual outcomes vary according to:
Patient age
Baseline skin condition
Degree of dehydration
Treatment area
Number of sessions
Treatment interval
Practitioner technique
Lifestyle
Individual biological response
No specific duration of effect should be guaranteed.
Storage & Handling
Hyaron® should be stored according to the manufacturer's current recommendations and the information supplied with the original product.
To maintain product integrity:
Keep unused product within its original packaging.
Store in a cool, dry place in accordance with manufacturer guidance.
Protect from direct sunlight.
Inspect each syringe and the outer packaging before use.
Check the batch number and expiry date.
Verify product authenticity and traceability.
Maintain appropriate aseptic handling procedures.
Do not use if sterile packaging is damaged.
Do not use if the syringe appears compromised.
Do not use after the stated expiry date.
Each syringe is intended for single use according to the manufacturer's Instructions for Use.
Important Information
Hyaron® is intended strictly for use by appropriately qualified and trained medical or aesthetic professionals.
Professional knowledge of the following is essential:
Relevant facial and treatment-area anatomy
Injectable skin-rejuvenation techniques
Mesotherapy techniques where applicable
Appropriate treatment planes
Patient selection
Aseptic practice
Complication prevention
Adverse-event recognition
Appropriate complication management
Patient Assessment
Treatment should only proceed following:
Full medical consultation
Review of medical history
Assessment of skin condition
Examination of the proposed treatment area
Review of previous aesthetic procedures
Assessment of contraindications
Discussion of expected outcomes
Explanation of potential adverse effects and complications
Completion of appropriate documented informed consent
Contraindications & Precautions
According to the supplied information, treatment may be unsuitable for individuals with:
Active infection or inflammation within the proposed treatment area
Pregnancy or breastfeeding
Bleeding disorders
Active dermatological conditions
Known hypersensitivity to any product component
Impaired wound healing
Recent cosmetic procedures requiring an appropriate healing interval
Other contraindications identified during professional assessment
This list should not be considered exhaustive.
Always consult the manufacturer's current Instructions for Use for the complete contraindication, warning and precaution profile.
Potential Treatment Reactions
Temporary treatment-related effects may include:
Redness
Swelling
Bruising
Tenderness
Mild discomfort
Temporary injection-site papules
Localised itching
These effects are generally associated with injectable procedures; their incidence and duration may vary.
More significant complications may also occur with injectable aesthetic treatments.
The supplied information references potential complications including:
Infection
Delayed inflammatory reactions
Vascular compromise
Tissue injury
Practitioners should be appropriately trained in complication recognition and management and provide patients with comprehensive written aftercare instructions.
Always consult the manufacturer's current Instructions for Use for complete information regarding indications, contraindications, warnings, precautions, administration and potential adverse events.
Do not use the product where:
Sterile packaging is damaged
A syringe appears compromised
The product has passed its expiry date
Product integrity is in doubt
Authenticity or traceability cannot be established
For appropriately qualified professional use only.
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