Want a Chiseled Jawline?

(Without any surgery?)

Say goodbye to that double chin. Kybella® is an FDA-approved injection designed to dissolve stubborn under-the-chin fat (submental fat). Within one to two visits, you will see a younger looking, more refined, beautiful profile. May Only, One Vial, $600 (Regularly $750) (Suggested purchase 3 vials for best results)

Kybella + Botox Special

Combine Kybella and Botox on the same day and receive 20 units of Botox for free

Simply Ageless

Your home-care regimen is just as important as your treatments at Honolulu MedSpa. Are you stocked up on the essentials?

This Month:

• 2 TNS Essential Serum
• 1 Retinol
• 1 Total Defense and Repair of your choice

+ Receive a complimentary Hydrafacial or Oxygen Facial on us! Total savings up to $160.

Please call 808-528-0888 or visit HonoluluMedSpa.com for details. Book today!

Important Safety Information:

KYBELLA® Professional ISI

Indication

KYBELLA® (deoxycholic acid) injection is indicated for improvement in the appearance of moderate to severe convexity or fullness associated with submental fat in adults.

The safe and effective use of KYBELLA® for the treatment of subcutaneous fat outside the submental region has not been established and is not recommended.

Important Safety Information

Contraindications

KYBELLA® is contraindicated in the presence of infection at the injection sites.

Warnings and Precautions

Marginal Mandibular Nerve Injury

Cases of marginal mandibular nerve injury, manifested as an asymmetric smile or facial muscle weakness, were reported in 4% of subjects in the clinical trials; all cases resolved spontaneously (range 1-298 days, median 44 days). KYBELLA® should not be injected into or in close proximity to the marginal mandibular branch of the facial nerve.

Dysphagia

Dysphagia occurred in 2% of subjects in the clinical trials in the setting of administration-site reactions, eg, pain, swelling, and induration of the submental area; all cases of dysphagia resolved spontaneously (range 1-81 days, median 3 days). Avoid use of KYBELLA® in patients with current or prior history of dysphagia as treatment may exacerbate the condition.

Injection-Site Hematoma/Bruising

In clinical trials, 72% of subjects treated with KYBELLA® experienced hematoma/bruising. KYBELLA® should be used with caution in patients with bleeding abnormalities or who are currently being treated with antiplatelet or anticoagulant therapy as excessive bleeding or bruising in the treatment area may occur.

Risk of Injecting Into or in Proximity to Vulnerable Anatomic Structures

To avoid the potential of tissue damage, KYBELLA® should not be injected into or in close proximity (1 cm-1.5 cm) to salivary glands, lymph nodes, and muscles.

Adverse Reactions

The most commonly reported adverse reactions in the pivotal clinical trials were: injection site edema/swelling, hematoma/bruising, pain, numbness, erythema, and induration.

Please see KYBELLA® full prescribing information