Restylane Kysse — OBT Technology Lip Filler with Built-In Lidocaine
The Restylane line’s dedicated lip filler — designed from the ground up for lip augmentation and the perioral zone. Restylane Kysse uses Galderma’s OBT / XpresHAn Technology to balance soft, kissable lip texture with sustained shape retention. FDA approved for lip augmentation and correction of upper perioral wrinkles in patients over 21. 20 mg/mL HA + 3 mg/mL lidocaine premixed for comfort.
Last reviewed: May 2026 · Manufacturer: Q-Med AB / Galderma, Uppsala, Sweden
Optimal Balance Technology — Built for Movement, Not Rigidity
Monophasic Gel Structure
Unlike NASHA’s particle-based biphasic gel, OBT produces a single continuous monophasic structure. This integrates seamlessly with surrounding tissue rather than sitting as discrete particles — reducing the palpable “bolus” feel in dynamic facial zones.
Flexibility for Expression
OBT-technology fillers (Refyne, Defyne, Volyme, Kysse, Contour) are engineered to flex with facial movement. The gel maintains shape at rest but yields with smiling, speaking, and natural animation — preserving the patient’s expressive identity.
Galderma Heritage
Manufactured by Q-Med AB in Uppsala, Sweden — the company that launched the world’s first HA dermal filler (Restylane, 1996). Over 40 million Restylane treatments performed globally across the NASHA and OBT product lines.
Restylane Kysse Active Ingredients
Cross-Linked Hyaluronic Acid
Stabilized hyaluronic acid at 20 mg/mL — the standard concentration across the Restylane portfolio. The HA is non-animal, produced by bacterial fermentation, and cross-linked using Galderma’s OBT Technology. Phosphate-buffered saline at pH 7 carries the gel.
Lidocaine HCl
Premixed local anaesthetic at the industry-standard 0.3% concentration. Reduces injection-site discomfort and eliminates the need for on-site mixing with separate lidocaine vials. The lidocaine itself wears off within hours of injection and does not affect long-term gel duration.
Where Restylane Kysse Is Used
Lip Body Augmentation
Primary FDA indication. Restylane Kysse’s OBT gel structure delivers soft, kissable lip texture rather than the firm projection of NASHA technology. Patients report natural lip movement during smiling and speaking.
Lip Border Definition
Vermillion border definition without the rigid ‘duck lip’ projection that can occur with firmer fillers. The product integrates with native lip tissue for a defined but flexible border.
Upper Perioral Wrinkles
Smoker’s lines / lipstick lines above the upper lip — Restylane Kysse’s second FDA indication. Fine-cannula technique recommended for this delicate zone.
Cupid’s Bow Enhancement
Off-label refinement of the cupid’s bow shape. The OBT gel’s flexibility makes it well-suited to maintaining natural lip animation.
Restylane Kysse vs Juvederm vs Belotero
| Feature | Restylane Kysse | Juvederm (Allergan) | Belotero (Merz) |
|---|---|---|---|
| HA Concentration | 20 mg/mL | 15–24 mg/mL | 20–26 mg/mL |
| Cross-Linking Tech | OBT® Technology | Vycross / Hylacross | CPM® Polydensified |
| Gel Structure | Monophasic (integrative) | Monophasic | Polydensified gradient |
| Lidocaine | 0.3% (premixed) | 0.3% (XC lines) | 0.3% |
| Origin | Sweden (Galderma / Q-Med) | USA (Allergan / AbbVie) | Germany (Merz) |
| Established Since | 1996 (first HA filler) | 2006 | 2005 |
| Distinctive Strength | Natural movement, flexibility | Long duration, high G-prime | Tissue integration, soft feel |
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Comparison based on manufacturer published data. See our top dermal filler comparison guide for broader market context.
Restylane Kysse Product Specifications
Brand & Origin
- Brand: Restylane (Galderma)
- Manufacturer: Q-Med AB
- Country of Origin: Uppsala, Sweden
- Audience: Licensed practitioners
Formula
- HA Source: Non-animal bacterial fermentation
- HA Concentration: 20 mg/mL stabilized
- Lidocaine: 3 mg/mL (0.3%) premixed
- Technology: OBT® Technology
Performance
- Duration: Up to 12 months
- Injection Depth: Lip body (submucosal), perioral dermis
- Recommended Needle: 30G ultra-thin wall typical
- Approval: FDA approved (lip augmentation + upper perioral wrinkles)
Packaging & Storage
- Packaging: 1 × 1 mL pre-filled syringe + needles
- Storage: 2–25 °C, do not freeze
- Shelf life: 24 months unopened
- Use: Single-use sterile
For market pricing context, see our dermal filler pricing guide.
Restylane Kysse — Frequently Asked Questions
What is Restylane Kysse?
Restylane Kysse is a Galderma hyaluronic acid dermal filler designed specifically for the lips and perioral area. It uses OBT / XpresHAn Technology — a monophasic cross-linking process that produces a soft, flexible gel suited to lip movement. The product contains 20 mg/mL of cross-linked HA and 3 mg/mL (0.3%) lidocaine for injection comfort. It is FDA approved for lip augmentation and correction of upper perioral wrinkles in patients over 21.
How is Restylane Kysse different from Restylane Lidocaine 1ml for lip enhancement?
The classic Restylane (with lidocaine) uses NASHA Technology — a biphasic, particle-based gel that provides firmer projection. Restylane Kysse uses OBT / XpresHAn Technology — a monophasic gel built for movement and natural expression. For patients wanting maximum lip volume and projection, classic Restylane is often selected. For patients prioritising soft, natural lip movement during smiling and speaking, Kysse is typically the better fit. Both share the same 20 mg/mL HA concentration.
How long does Restylane Kysse last in the lips?
Per Galderma clinical data, Restylane Kysse delivers up to 12 months in the lip body — significantly longer than the 6-month average for many competing lip fillers. The product also showed strong performance for upper perioral wrinkles. Individual duration depends on dose, lip animation intensity, patient metabolism, and injection technique.
Is Restylane Kysse FDA approved?
Yes. Restylane Kysse received FDA approval for lip augmentation in 2020, with subsequent approval for upper perioral wrinkles. It is one of the most clinically documented lip fillers on the US market and carries dual FDA indications.
What needle gauge is used for Restylane Kysse?
Practitioners typically use a 30G ultra-thin wall needle or a blunt-tip 30G cannula for lip body placement. The supplied needles in the syringe blister pack are 30G typical. Fine-cannula technique is generally recommended for the upper perioral zone to minimise bruising in this thin-skinned area.
Can Restylane Kysse be used outside the lips?
While the FDA approval is specifically for lip augmentation and upper perioral wrinkles, the OBT gel structure makes Kysse a viable off-label choice for fine perioral lines, philtrum definition, and cupid’s bow refinement. Off-label use is at the practitioner’s clinical discretion within scope of practice.
Where is Restylane Kysse manufactured?
Restylane Kysse is manufactured by Q-Med AB, a Galderma subsidiary based in Uppsala, Sweden. The Restylane brand spans over 25 years of clinical history with more than 40 million treatments performed globally.
Can Restylane Kysse be combined with other Restylane products in the same session?
Yes. A common full-face protocol uses Restylane Kysse for lips and upper perioral wrinkles in combination with Restylane Defyne or Restylane Refyne in the nasolabial folds and marionette lines. All Restylane products share the same 20 mg/mL HA base concentration and have established compatibility documented in Galderma clinical studies.
How should Restylane Kysse be stored?
Store at 2-25 °C in original packaging, away from direct sunlight. Do not freeze. Shelf life is typically 24 months from manufacturing date when unopened. Once opened, contents must be used immediately — partial syringes cannot be retained.
Does Restylane Kysse contain animal-derived ingredients?
No. Restylane Kysse uses non-animal stabilized hyaluronic acid produced by bacterial fermentation. The product is contraindicated in patients with severe allergies to gram-positive bacterial proteins (used in fermentation) but contains no animal-derived proteins.
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Browse category →Read Before Clinical Use
Restylane Kysse is a prescription medical device for use only by licensed aesthetic practitioners. Common reactions include injection-site bruising, swelling, redness, and tenderness — generally resolving within days. Like all hyaluronic acid dermal fillers, treatment carries rare but serious vascular complication risks. Mid-dermal placement reduces but does not eliminate vascular risk. Contraindicated in patients with severe allergies to gram-positive bacterial proteins. Full contraindications, vascular complication protocols, aftercare, and emergency guidance are detailed on the dermal filler safety page.
Read Full Dermal Filler Safety Information →RESTYLANE is a registered trademark of Galderma S.A. Fillersfairy.com is a channel distributor and does not provide medical advice. This page is for informational purposes only and does not replace the manufacturer’s official Instructions for Use, which remains the authoritative source for clinical administration. Regulatory status varies by jurisdiction — buyers are responsible for verifying legal status before ordering.

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