XEOMIN® (incobotulinumtoxinA) IMPORTANT CONSUMER SAFETY INFORMATION

Read the Medication Guide before you start receiving XEOMIN (Zeo-min) and each time XEOMIN is given to you as there may be new information. The risk information provided here is not comprehensive.

To learn more:

• Talk to your health care provider or pharmacist.
• Visit www.xeominaesthetic.com to obtain the Full Prescribing Information and Medication Guide.
• Call 1-866-862-1211

Uses: XEOMIN is a prescription medicine that is injected into muscles and used to improve the look of moderate to severe upper facial lines (frown lines, forehead lines, and crow’s feet) in adults for a short period of time (temporary). Please see additional Important Safety Information below and Full Prescribing Information and Medication Guide at XeominAesthetic.com.

Warnings: XEOMIN may cause serious side effects that can be life threatening. Call your doctor or get medical help right away if you have any of these problems anytime (hours to weeks) after treatment with XEOMIN: 

• Problems with swallowing, speaking, or breathing can happen within hours to weeks after an injection of XEOMIN if the muscles that you use to breathe and swallow become weak. Death can happen as a complication if you have severe problems with swallowing or breathing after treatment with XEOMIN.
• People with certain breathing problems may need to use muscles in their neck to help them breathe and may be at greater risk for serious breathing problems with XEOMIN. 
• Swallowing problems may last for several months, and during that time you may need a feeding tube to receive food and water. If swallowing problems are severe, food or liquids may go into your lungs. People who already have swallowing or breathing problems before receiving XEOMIN have the highest risk of getting these problems. 
• Spread of toxin effects. In some cases, the effect of botulinum toxin may affect areas of the body away from the injection site and cause symptoms of a serious condition called botulism. The symptoms of botulism include: loss of strength and muscle weakness all over the body, double vision, blurred vision and drooping eyelids, hoarseness or change or loss of voice, trouble saying words clearly, loss of bladder control, trouble breathing, trouble swallowing. 

These symptoms can happen hours to weeks after you receive an injection of XEOMIN. These problems could make it unsafe for you to drive a car or do other dangerous activities. 

Do not use XEOMIN if you are allergic to XEOMIN or any of the ingredients in XEOMIN (see the end of this Guide for a list of ingredients in XEOMIN), had an allergic reaction to any other botulinum toxin products such as rimabotulinumtoxinB (MYOBLOC®), onabotulinumtoxinA (BOTOX®, BOTOX® COSMETIC), or abobotulinumtoxinA (DYSPORT®) or have a skin infection at the planned injection site. 

Before receiving XEOMIN, tell your doctor about all of your medical conditions, including if you: 

• have a disease that affects your muscles and nerves (such as amyotrophic lateral sclerosis [ALS or Lou Gehrig’s disease], myasthenia gravis or Lambert-Eaton syndrome).
• have had any side effect from any other botulinum toxin in the past.
• have a breathing problem such as asthma or emphysema.
• have a history of swallowing problems or inhaling food or fluid into your lungs (aspiration).
• have bleeding problems.
• have drooping eyelids.
• have plans to have surgery.
• have had surgery on your face.
• are pregnant or plan to become pregnant. It is not known if XEOMIN can harm your unborn baby.
• are breastfeeding or plan to breastfeed. It is not known if XEOMIN passes into breast milk.

Tell your doctor about all of the medicines you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Talk to your doctor before you take any new medicines after you receive XEOMIN.

Using XEOMIN with certain other medicines may cause serious side effects. Do not start any new medicines until you have told your doctor that you have received XEOMIN in the past. Especially tell your doctor if you:

• have received any other botulinum toxin product in the last four months.
• have received injections of botulinum toxin such as rimabotulinumtoxinB (MYOBLOC®), onabotulinumtoxinA (BOTOX®, BOTOX® COSMETIC) and abobotulinumtoxinA (DYSPORT®) in the past. Be sure your doctor knows exactly which product you received. The dose of XEOMIN may be different from other botulinum toxin products that you have received.
• have recently received an antibiotic by injection.
• take muscle relaxants.
• take an allergy or cold medicine.
• take a sleep medicine.

Ask your doctor if you are not sure if your medicine is one that is listed above. Know the medicines you take. Keep a list of your medicines with you to show your doctor and pharmacist each time you get a new medicine.

Possible Side Effects

XEOMIN can cause serious side effects that can be life threatening including allergic reactions. Symptoms of an allergic reaction to XEOMIN may include: itching, rash, redness, swelling, wheezing, asthma symptoms, or dizziness or feeling faint. Tell your doctor or get medical help right away if you get wheezing or asthma symptoms, or if you get dizzy or faint. See “Warnings.”

The most common side effect of XEOMIN in people with upper facial lines include:

• injection site bruising.

These are not all the possible side effects of XEOMIN. Call your doctor for medical advice about side effects. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit MedWatch or call 1-800-FDA-1088.

General information about the safe and effective use of XEOMIN

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. You can ask your pharmacist or doctor for information about XEOMIN that is written for health professionals.

Active Ingredient: botulinum toxin type A.

Inactive Ingredients: human albumin and sucrose.

RADIESSE® and RADIESSE® (+) are FDA-approved to smooth moderate to severe facial wrinkles and folds, such as nasolabial folds. RADIESSE (+) is also FDA-approved to improve moderate to severe loss of jawline contour in adults over the age of 21. RADIESSE® is also used for correcting volume loss in the back of the hands. Do not use RADIESSE and RADIESSE (+) if you have severe allergies with anaphylaxis, known hypersensitivity to any of the components, bleeding disorders, or a known hypersensitivity to lidocaine or anesthetics of the amide type. Delayed-onset inflammation at the site of injection following illness, infection, vaccinations, or dental procedures is a known side effect of dermal fillers. Common side effects seen in clinical studies of RADIESSE or RADIESSE (+) include bruising, redness, swelling, pain, itching, lumps/bumps at site of injection, difficulty chewing and other local side effects. These are not all the possible side effects with RADIESSE and RADIESSE (+). RADIESSE is available by prescription only – so ask your provider if RADIESSE is right for you. Please see the Patient Information Guide at www.radiesse.com for a list of these events and full safety information. Individual results may vary.

BELOTERO BALANCE® (+) is FDA-approved to smooth moderate to severe facial wrinkles and folds, such as nasolabial folds and improve the appearance of under-eye hollows in adults over the age of 21. Do not use BELOTERO BALANCE (+) if you have a skin infection or inflammation. Do not use BELOTERO BALANCE (+) if you have severe allergies or a history of allergic reactions to hyaluronic acid, local anesthetics such as lidocaine, or to small amounts of protein from bacteria. Delayed-onset inflammation at the site of injection following illness, infection, vaccinations, or dental procedures is a known side effect of dermal fillers. Common side effects seen in clinical studies with BELOTERO BALANCE® (+) include swelling, bruising, redness, nodules, pain, altered color or induration. These are not all the possible side effects with BELOTERO BALANCE (+). BELOTERO BALANCE (+) is available by prescription only – so ask your provider if BELOTERO BALANCE (+) is right for you. Please see the Patient Information Guide at www.belotero.com for a list of these events and full safety information. Individual results may vary.

The ULTHERA® System is U.S. FDA-cleared to lift the eyebrow, the skin on the neck and under the chin as well as to improve lines and wrinkles on the décolleté. The most common side effects reported in clinical trials were redness, swelling, pain and transient nerve effects. Reported adverse events from post-marketing surveillance are available in the Instructions for Use (IFU). Please see the IFU for product and safety information, including a full list of these events at Ultherapy.com/IFU. 

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