Updated: Jun 3
Halcyon Med Spa was the first in Corpus Christi and among the first in the U.S. to be offering this new FDA-approved HA lip filler that uses XpresHAn Technology (pronounced ex-spre-shan), which is designed for excellent tissue integration that allows individuals to maintain their natural-looking expressions.
Restylane Kysse is clinically proven to last for up to 1 year and is designed to provide shape and structure for people with lips that have thinned due to the aging process or for those seeking natural-looking, fuller lips. 78% of subjects reported that they saw improvements in both lips 48 weeks after treatment. Restylane Kysse was shown to be both safe and well-tolerated. It contains lidocaine as a medication used to numb the area to decrease pain and reduce discomfort associated with the lip area. Contact us at 361-452-2637 to learn more about this novel lip filler. You are always welcome to a completely free 15-minute to discuss your filler options with one of our licensed medical providers.
What to expect:
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Natural-looking, full, softer, and more kissable lips
Improved lip color
Results clinically proven to last up to 1 year
Restylane Kysse was evaluated in multiple clinical studies—a pivotal Phase 3 active comparator study, a European supportive active comparator study evaluating Restylane Kysse versus the control, as well as a Phase 4 study evaluating naturalness of expression, patient satisfaction, and novel claims around partner satisfaction.
All commonly reported adverse events (AEs) in the Restylane Kysse group were mild in intensity compared to the control group where majority of the late onset events were assessed as moderate in intensity.7,8 The most common temporary side effects include bruising, masses and nodules, hypersensitivity, redness, and swelling at the injection site.1 To learn more about serious but rare side effects and full Important Safety Information, visit RestylaneUSA.com.
Important Safety Information
Indication: Restylane® Kysse is indicated for injection into the lips for lip augmentation and for correction of upper perioral rhytids in patients over the age of 21. Restylane Kysse contains traces of gram-positive bacterial protein and is contraindicated for patients with allergies to such material or for patients with severe allergies that have required in-hospital treatment. Restylane Kysse should not be used by patients with bleeding disorders, with hypersensitivity to amide-type local anesthetics, such as lidocaine, or by women who are pregnant or breastfeeding.
Use of Restylane Kysse at the site of skin sores, pimples, rashes, hives, cysts, or infection should be postponed until healing is complete. The most commonly observed side effects are swelling, tenderness, bruising, pain, and redness at the injection site.
These are typically mild in severity and usually resolve within 7 days after treatment. Serious but rare side effects include delayed onset infections, recurrence of herpetic eruptions, and superficial necrosis and scarring at the injection site. Do not implant into blood vessels. Use with caution in patients recently treated with anticoagulant or platelet inhibitors to avoid bleeding and bruising.
Treatment volume should be limited to 1.5 mL per lip per treatment and 1.0 mL for upper perioral rhytid correction, as greater amounts significantly increase moderate and severe injection site reactions. The safety or effectiveness of treatment in areas other than lips and upper perioral rhytids has not been established in controlled clinical studies.
Restylane Kysse is only available through a licensed practitioner. Complete Instructions for Use are available at www.RestylaneKysse.com.