RRS® HA Eyes ( 12 x 1.5 mL) | Skin Tech Pharma Group (Spain)
Short Description
Detailed Description
RRS® HA Eyes is a sterile, non-pyrogenic, absorbable intradermal injectable manufactured in Spain by Skin Tech Pharma Group (Aesthetic Dermal). Operating under strict European medical device directives (CE 1014), it is formulated to address the multifactorial nature of periorbital aging—where vascular congestion, lymphatic stagnation, skin thinning, and pigment accumulation intersect in an anatomically vulnerable space.
The formulation utilizes a multi-targeted biological matrix:
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Physiological Hyaluronic Acid Base (5.0 mg/mL): Uncross-linked, non-animal bio-fermented sodium hyaluronate replenishes the extracellular matrix of the infraorbital dermis. It restores hydraulic balance, smooths superficial dehydration crinkles, and acts as a biocompatible delivery vehicle for active bio-nutrients without causing excessive water retention or malar festooning.
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Vasoactive & Lymphatic Drainage Complex (Anti-Bag Action):
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Ruscus Aculeatus (Butcher’s Broom Extract): Rich in ruscogenins, it acts as a selective venotonic that strengthens capillary walls, reduces microvascular hyperpermeability, and limits transudate pooling.
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Melilotus Officinalis (Sweet Clover Extract): Delivers natural coumarins that stimulate lymphatic motoricity and macrophage proteolysis, accelerating the clearance of protein-rich fluid from stagnant under-eye bags.
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Troxerutin & Hesperidin Methyl Chalcone: Bioflavonoids that reinforce endothelial cell junctions, reduce erythrocyte extravasation, and decrease capillary fragility.
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Depigmenting & Antioxidant Shield (Dark Circle Resolution):
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Vitamin C & Resveratrol: Neutralize free radicals induced by UV and oxidative stress, suppress melanin overproduction, and lighten hemosiderin deposits caused by extravasated red blood cells.
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Flavonoids (Naringin, Quercetin, Polyphenols): Inhibit collagenase and elastase enzymes while reducing localized neurogenic inflammation.
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Dermal Redensifying Matrix (Organic Silicon & Peptides):
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Organic Silicon (Silanol): Stimulates fibroblast proliferation and stabilizes structural glycosaminoglycan (GAG) networks, thickening the translucent periorbital skin to help conceal underlying dark vascular beds.
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Treatment Areas & Indications
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Infraorbital Dark Circles (Periorbital Dyschromia):
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Vascular Dark Circles: Bluish, purplish, or red discoloration caused by sluggish capillary microcirculation and thin, translucent lower eyelid skin
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Pigmentary Dark Circles: Brownish epidermal and dermal melanin accumulation around the eye socket
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Structural Shadowing: Visual darkening accentuated by early tear trough hollows
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Lymphatic Under-Eye Bags & Morning Puffiness:
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Fluid retention and edematous swelling of the lower eyelids secondary to poor lymphatic return
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Post-sleep periorbital congestion
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Lower Eyelid & Lateral Canthal Skin Aging:
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Crepey, paper-thin cutaneous texture and superficial dehydration crinkles
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Dynamic and fine static lateral canthal lines (crow’s feet)
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Pre- & Post-Blepharoplasty Optimization:
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Conditioning delicate eyelid tissue prior to surgical blepharoplasty
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Managing residual post-operative micro-edema and bruising
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Key Clinical Advantages
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CE Class III Medical Device Certification: Manufactured under rigorous European pharmaceutical directives (CE 1014), guaranteeing safety and batch purity for direct periorbital intradermal injection.
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Zero Malar Festoon / Edema Risk: Formulated with non-cross-linked HA combined with lymphatic draining botanicals, eliminating the chronic fluid retention often seen with cross-linked BDDE gel fillers.
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Zero Tyndall Discoloration: Integrates transparently into the tissue, leaving no blue discoloration even when deposited superficially in the thin lower eyelid.
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Dual Action (Decongestion + Thickening): Concurrently clears stagnant lymphatic fluid and thickens the dermal barrier to obscure deep underlying orbital vasculature.
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Versatile Delivery Profile: Compatible with precision 32G/34G micro-papular needles, multi-injector mesotherapy devices, or blunt-tip microcannulas.
Clinical Administration & Delivery Protocols
| Technique | Recommended Instrument | Injection Plane | Administration Method |
| Micro-Papular Needle (Standard) | 32G or 34G x 4 mm micro-meso needle | Superficial to mid-dermis (0.5–1.0 mm depth) | Micro-boluses of 0.01–0.02 mL per point, spaced 2–4 mm apart along the infraorbital rim and crow’s feet (approx. |
| 0.5–0.75 mL per eye) | Blunt Microcannula (Advanced) | 30G or 27G x 25 mm blunt cannula | Sub-orbicularis oculi / deep subcutaneous plane | Single lateral entry at the zygomatic arch; retrograde linear fan distribution across the infraorbital margin | Microneedling / MTS | Automated microneedling pen | Epidermal-dermal junction (0.25–0.5 mm depth) | Gentle transdermal micro-channeling around the orbital rim (avoiding mobile upper eyelid) |
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Standard Clinical Protocol: 4 to 6 sessions spaced 1 to 2 weeks apart.
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Maintenance Schedule: 1 session every 3 to 4 months to preserve microvascular and lymphatic tone.
Technical Specifications
| Parameter | Specification |
| Product Classification | Injectable Periorbital Biorevitalizer / CE Class III Medical Device |
| Manufacturer / Origin | Skin Tech Pharma Group / Aesthetic Dermal (Girona, Spain) |
| Hyaluronic Acid Profile | Non-cross-linked sodium hyaluronate (5.0 mg/mL / 7.5 mg per ampoule) |
| Active Biorevitalizing Complex | 27.3 mg/mL solution: Ruscus aculeatus, Melilotus officinalis, Troxerutin, Escin, Hesperidin, Vitamin C, Resveratrol, Organic Silicon, Polyphenols |
| Lidocaine Content | Lidocaine-free (compatible with pre-procedural topical anesthetic cream) |
| Packaging Presentation | Box of 4 ampoules x 1.5 mL (6.0 mL total) or Clinic Pack of 12 ampoules x 1.5 mL (18.0 mL total) |
| Target Injection Planes | Superficial dermis, epidermal-dermal junction, or sub-orbicularis plane |
| Papule Resolution Time | Typically flattens and absorbs within 12 to 24 hours post-injection |
| Expected Clinical Duration | 4 to 6 months cumulative improvement following a complete series |
| Storage Instructions | Store between 2°C and 30°C (36°F to 86°F); protect from direct heat, sunlight, and freezing |
| Regulatory Category | CE-marked Class III Medical Device (CE 1014) / Prescription Only (Rx) |
Comparative Benchmark: Leading Periorbital Injectables
| Feature | RRS® HA Eyes (Skin Tech) | Jalupro® Young Eye (Prof. Derma) | Lumi Eyes (Dermagen) | PhilArt Eye (Croma) |
| Primary Active Mechanism | Non-cross HA + Ruscus / Melilotus flavonoids | Bi-density HA + 7 Amino Acids + 3 Peptides | Salmon Polynucleotide (PDRN 2 mg/mL) | High-purification Polynucleotide (PN 15 mg/2 mL) |
| Target Focus | Vascular dark circles, lymphatic puffiness & bags | Structural thinning, ligament descent, accordion wrinkles | Cellular DNA repair, brightening, micro-lines | Fibroblast biostimulation, skin thickening, elasticity |
| Anti-Puffiness Action | Very High (Venotonic & lymphatic drainers) | Moderate (Acetyl Tetrapeptide-5) | Low (Pure regenerative DNA) | Low (Pure regenerative PN) |
| Presentation | 4 x 1.5 mL ampoules | 1 x 1.0 mL pre-filled syringe | 1 x 1.0 mL pre-filled syringe | 1 x 2.0 mL pre-filled syringe |
| Regulatory Status | CE Class III Injectable | CE Class III Injectable | CE / KFDA Certified | CE Class III Injectable |
Professional Advisory: RRS® HA Eyes is a CE Class III medical device intended strictly for certified aesthetic physicians, dermatologists, and plastic surgeons trained in periorbital anatomy and micro-injection techniques. Injection inside the orbital septum, into herniated retroseptal fat pads, or directly intravascularly is strictly contraindicated. Patients should avoid aspirin, NSAIDs, and anticoagulants for 48 hours prior to treatment to minimize periorbital petechiae and bruising.






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