BOTOX® Cosmetic is the first and only FDA-approved product to temporarily improve both moderate to severe frown lines between the brows and crow’s feet lines around the sides of the eyes in adults.

BOTOX® Cosmetic targets one of the underlying causes of frown lines and crow’s feet—the repeated muscle contractions from frowning and squinting over the years. Your doctor will inject these muscles with BOTOX® Cosmetic to temporarily reduce muscle activity. You’ll begin to notice a visible smoothing of these lines.

To temporarily improve moderate to severe crow’s feet, your doctor will inject BOTOX® Cosmetic into the muscle surrounding the sides of your eyes—called the orbicularis oculi.

For temporary improvement of moderate to severe frown lines, BOTOX® Cosmetic is injected into 2 muscles—the corrugator and procerus muscles.

Treatment with BOTOX® Cosmetic takes approximately 10 minutes and requires minimal downtime or recovery—it’s often called a lunchtime procedure.

Think 2 treatments, 1 visit. Ask your doctor aboutreceiving BOTOX® Cosmetic for moderate to severe frown lines and crow’s feet at the same time.

When BOTOX® Cosmetic is administered by an experienced injector, you should not lose the ability to show expressions. BOTOX® Cosmetic is a techniquesensitive procedure that should only be performed by a licensed and trained aesthetic provider who has expertise in facial anatomy.

Talk to your doctor about your expectations and the results you want to achieve with treatment.

BOTOX® Cosmetic (onabotulinumtoxinA) Important Information

For full product information including important prescribing and safety information, please click here.

The JUVÉDERM® range of fillers can correct age-related loss in the cheeks, lips, lip lines, and other facial wrinkles and folds in individuals over the age of 21.

JUVÉDERM® is the world's #1 selling dermal filler collection, and with good reason! JUVÉDERM® is FDA-Approved, so you can rest assured that it is safe. Using JUVÉDERM® offers:

• Instant results
• Nonsurgical treatments
• Natural-looking, long-lasting results
• In-office procedures

JUVÉDERM® Collection of Fillers Important Information

For full safety information, please click here.

RADIESSE® and RADIESSE® (+) are dermal fillers that are used for smoothing moderate to severe facial wrinkles and folds, such as nasolabial folds (the creases that extend from the corner of your nose to the corner of your mouth). RADIESSE® is also used for correcting volume loss in the back of the hands.

Who should not use RADIESSE® or RADIESSE® (+)?

You should not use RADIESSE® or RADIESSE® (+) if you have an allergy to any component of the product, if you have a history of severe allergies, if you have a bleeding disorder, or if you are pregnant or breastfeeding. You should not use RADIESSE® (+) if you have an allergy to lidocaine or medicines like it.

What is the most important information I should know about RADIESSE® and RADIESSE® (+)?

One of the risks with using these products is unintentional injection into a blood vessel. The chances of this happening are very small, but if it does happen, the complications can be serious, and may be permanent. These complications, which have been reported for facial injections, can include vision abnormalities, blindness, stroke, temporary scabs, or permanent scarring of the skin. If you have changes in your vision, signs of a stroke (including sudden difficulty speaking, numbness or weakness in your face, arms, or legs, difficulty walking, face drooping, severe headache, dizziness, or confusion), white appearance of the skin, or unusual pain during or shortly after treatment, you should notify your health care practitioner immediately.

As with all procedures that involve an injection through the skin, there is a risk of infection.

Do not use RADIESSE® or RADIESSE® (+) if you have a skin infection until it has healed.

It is not known if RADIESSE® or RADIESSE® (+) is safe or effective in the lips, or in the area around the eyes.

The microspheres in RADIESSE® and RADIESSE® (+) can be seen in X-rays and CT Scans. It is very important that you tell your health care provider that you have had RADIESSE® or RADIESSE® (+) dermal filler.

If you have a history of herpes, you may experience a herpes breakout after receiving RADIESSE® or RADIESSE® (+).

Injection in the back of the hand may result in temporary difficulty performing activities. RADIESSE® may cause nodules, bumps or lumps in the back of the hand and can last up to 1 year.

You should minimize strenuous activity and avoid extensive sun or heat exposure for about 24 hours after treatment and until any swelling or redness has resolved.

What should I tell my doctor before using RADIESSE® or RADIESSE® (+)?

Tell your health care provider if you are taking blood thinners or medicines that can interfere with the clotting of blood, such as aspirin or warfarin. These medicines might make it more likely that you will experience bruising or bleeding at the injection site. Tell your health care provider if you have any diseases, injuries or disabilities of the hand, if you have a history forming large, raised scars or if you have had any other skin treatments such as skin peels.

What are the most common adverse events with RADIESSE® or RADIESSE® (+)?

The most common adverse events seen in clinical studies of RADIESSE® used in the hands include bruising, redness, swelling, pain, itching, nodules or bumps/lumps, difficulty performing activities, loss of sensation and other local side effects. The most common adverse events seen in clinical studies of RADIESSE® or RADIESSE® (+) used in the face include bruising, redness, swelling, pain, itching and other local side effects.

These are not all of the possible side effects with RADIESSE® or RADIESSE® (+). Merz collects information about adverse events seen with RADIESSE® and RADIESSE® (+) outside of clinical studies. These events are included in the RADIESSE® and RADIESSE® (+) Patient Information Guide based on an assessment of seriousness and potential causal relationship to RADIESSE® or RADIESSE® (+). Please see the Patient Information Guide available at www.radiesse.com for list of these events. Tell your health care provider about any side effects that bother you or do not go away.

Important: For full safety information, please visit www.Radiesse.com or call MyMerz Solutions at 1-844-469-6379

RADIESSE® and RADIESSE® (+) are available by prescription only.

Deoxycholic acid is a naturally occurring molecule that helps break down the fat in the body. The active ingredient in Kybella® is synthetic deoxycholic acid. Fat cells are broken down each time Kybella® is injected into the treatment area beneath the chin. Over a period of time, those cells are cleared away through the natural processes of your body. You are left with a noticeable reduction in fullness under the chin.

We will recommend the number of treatment sessions you may need to achieve your aesthetic goals. The injection process may take 15 to 20 minutes. Each treatment is at least 1 month apart.

Sometimes serious side effects can occur, including:

• Nerve injury in the jaw that can temporarily (median 44 days) cause an uneven smile or facial muscle weakness (experienced by 4 out of 100 people in clinical studies)
• Trouble swallowing (experienced by 2 out of 100 people in clinical studies)
• Possible injection-site problems that include bruising, hair loss, open sores (ulcers), and tissue damage and necrosis around the injection site

The most common side effects include: swelling, numbness, redness, pain, and areas of hardness. Swelling is an expected reaction to treatment, but generally becomes less severe with subsequent treatments.

KYBELLA® (deoxycholic acid) injection 10 mg/mL Important Information:

For full safety information, please click here.