CALIFORNIA SUPPLY CHAIN ACT

The California Transparency in Supply Chain Act of 2010 was designed to increase the amount of information made available by manufacturers and retail sellers regarding efforts to address the issue of slavery and human trafficking in their direct supply chain thereby allowing consumers to make more informed choices regarding the products they purchase and the companies they choose to support through their purchases.

This disclosure identifies the steps ZELTIQ® Aesthetics, Inc. (“ZELTIQ”) takes to eradicate slavery and human trafficking in its direct supply chain. As a manufacturer of medical devices, ZELTIQ is committed to the goals of this legislation and ensuring that the materials it uses in its CoolSculpting® products are sourced from socially responsible suppliers. Most of ZELTIQ’s manufacturing is done domestically and these operations are subject to and compliant with federal, state, and local labor laws. Additionally, most of the members of ZELTIQ’s direct supply chain are based in the United States.

Supplier Verification
Key members of various departments sit on ZELTIQ’s Disclosure Committee. The Disclosure Committee meets quarterly to discuss potential risks and disclosures, which may include those risks related to suppliers, slavery and human trafficking. The members of the Disclosure Committee, in turn, relay the information collected to others within their respective departments to solicit additional relevant information. ZELTIQ does not specifically verify its direct supply chain to evaluate risks of slavery and human trafficking.

Supplier Audits
ZELTIQ is subject to regulation by the United States Food and Drug Administration and, as part of its quality system, ZELTIQ is required to regularly audit its main suppliers. ZELTIQ performs audits of its main suppliers annually and/or biennially to ensure the supplier’s compliance with ZELTIQ’s quality system. Although these audits are not specific to slavery and human trafficking, ZELTIQ visits these suppliers’ locations and is able to inspect the supplier on a holistic basis.

Supplier Certification
ZELTIQ expects all of its direct suppliers to abide by all governing laws, including, but not limited to, local, state, federal, national, and international laws and regulations, as well as ZELTIQ’s company policies. At this time, ZELTIQ does not specifically require its suppliers to certify that the materials incorporated into the products they supply to ZELTIQ comply with the laws regarding slavery and human trafficking of the country or countries in which they are doing business. If ZELTIQ is alerted to potential issues with its direct supply chain, it will take appropriate actions.

Internal Accountability
ZELTIQ is committed to its own full compliance with the laws and regulations of the cities, states, and countries in which it operates. ZELTIQ’s Corporate Code of Business Conduct requires that each employee in the United States and internationally comply with all applicable laws and regulations, which would include those governing compliance with slavery and human trafficking. All employees are expected to report any suspected violation of the Code of Business Conduct. To that end, ZELTIQ has established a Whistleblower Hotline. Customers, employees, or other interested parties are able to use the Whistleblower Hotline to provide anonymous information about ZELTIQ and members of its direct supply chain, including grievances or other information related to slavery and human trafficking in its direct supply chain. ZELTIQ investigates potential violations and takes remedial and/or disciplinary steps as appropriate.

Training
All of ZELTIQ’s employees are trained on all of its policies and procedures, including its Corporate Code of Business Conduct. ZELTIQ is committed to working with members of its direct supply chain and its employees to meet ZELTIQ’s high standards for business ethics, integrity and values, and respect for human rights.

USES & IMPORTANT SAFETY INFORMATION

USES & IMPORTANT SAFETY INFORMATION FOR
COOLSCULPTING ELITE & COOLTONE

CoolSculpting® and CoolSculpting® Elite Uses

CoolSculpting® and CoolSculpting® Elite are FDA-cleared for the treatment of visible fat bulges in the submental (under the chin) and submandibular (under the jawline) areas, thigh, abdomen, and flank, along with bra fat, back fat, underneath the buttocks (also known as banana roll), and upper arm. It is also FDA-cleared to affect the appearance of lax tissue with submental area treatments. CoolSculpting® and CoolSculpting® Elite are not treatments for weight loss.

CoolSculpting® and CoolSculpting® Elite Important Safety Information

These procedures are not for everyone. You should not be treated with CoolSculpting® or CoolSculpting® Elite if you suffer from cryoglobulinemia, cold agglutinin disease, or paroxysmal cold hemoglobinuria.

Tell your doctor if you have any medical conditions including recent surgery, pre-existing hernia, and any known sensitivities or allergies.

During the procedure you may experience sensations of pulling, tugging, mild pinching, intense cold, tingling, stinging, aching, and cramping at the treatment site. These sensations lessen as the area becomes numb. Following the procedure, typical side effects include temporary redness, swelling, blanching, bruising, firmness, tingling, stinging, tenderness, cramping, aching, itching, or skin sensitivity, and sensation of fullness in the back of the throat after submental or submandibular area treatment.

Rare side effects may happen in 1 to 10 out of 10,000 CoolSculpting® and CoolSculpting® Elite treatments (between 0.01% to 0.1%). One such rare side effect is a visible enlargement in the treated area, which may develop 2 to 5 months after treatment, will not resolve on its own, and may require surgical intervention for correction.

Please see full Important Safety Information for CoolSculpting® and CoolSculpting® Elite on CoolSculpting.com.

Patient Results May Vary.

CoolTone® Uses

The CoolTone® device is FDA-cleared for improvement of abdominal tone, strengthening of the abdominal muscles, and development for firmer abdomen. CoolTone® is also FDA-cleared for strengthening, toning, and firming of buttocks and thighs.

CoolTone® Important Safety Information

The CoolTone® procedure is not for everyone. You should not have the CoolTone® treatment in areas with metal, electrical, or electronic implants/devices like cardiac pacemakers, implanted hearing devices, implanted defibrillators, implanted neurostimulators, drug pumps, or hearing aids.

Tell your doctor if you have any medical conditions as CoolTone® should not be used over a menstruating uterus, over areas of the skin that lack normal sensation, in patients with fever, malignant tumor, hemorrhagic conditions, epilepsy, recent surgical procedure, pulmonary insufficiency, or pregnancy.

CoolTone® should be used with caution in patients with Graves' disease (an autoimmune disorder that causes overactive thyroid), active bleeding disorders, or seizure disorders.

Women who are close to menstruation may find that it comes sooner, or cramping is increased or intensified with CoolTone® treatments, therefore, it is recommended to not undergo treatment during this time of the month.

CoolTone® should not be used in the heart or head areas, areas of new bone growth, over the carotid sinus nerves, or over the neck or mouth. CoolTone® should not be applied over swollen, infected, inflamed areas or skin eruptions. Caution should be used for patients with suspected or diagnosed heart problems.

Common side effects may include, but may not be limited to, muscular pain, temporary muscle spasm, temporary joint or tendon pain, and redness at or near the treatment site.

Ask your Healthcare Provider if CoolTone® is right for you.

Please see full Important Safety Information for additional information at coolsculpting.com/cooltone.

Patient Results May Vary.