Sculptra.com: For Healthcare Professionals - Get Listed in Our Healthcare Provider Locator

FOR U.S. RESIDENTS ONLY

	How Sculptra® Works
	Volumetric Improvement
	Safety and Tolerability
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	Product Information

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Information for Healthcare Providers Wishing to be Listed on Sculptra.com

As a service to those seeking treatment with Sculptra®, Dermik lists healthcare providers who have incorporated Sculptra® into their practices. This service is not intended as a recommendation, referral, or endorsement of any particular healthcare provider or practice, or as a tool for verifying credentials, qualifications, or abilities. Dermik does not guarantee the accuracy of the listings, as healthcare providers are responsible for providing current contact information.

Requirements for being listed
Healthcare providers who have incorporated Sculptra® into their practices are eligible to be listed on Sculptra.com. In order to be listed, you must obtain, complete, and return by fax a listing permission form that can be obtained from a sales consultant or Besse Medical. Your listing will appear on Sculptra.com within 10 business days of Dermik Aesthetics receiving your completed form.

Information contained in listings
Listings consist of basic contact information: healthcare professional name, practice name (optional), street address, and phone number. Listings do not include email or website addresses.

Listings in search results
Search results are based purely on the calculated distance between the practices in our database and the address a user provides when searching. The results are listed in order of increasing distance from the user's address to the practice address.

Please visit Besse Medical or call 1-888-7-SCULPTRA (1-888-772-8578) to order Sculptra® for your practice.

Sculptra® is injected into the skin for restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus.

IMPORTANT SAFETY INFORMATION

Sculptra® is contraindicated in those individuals who have shown a hypersensitivity to any of its components. Sculptra® should not be injected in areas with active skin infection or inflammation. Avoid injection into the blood vessels.

The most commonly observed adverse event was the delayed occurrence of subcutaneous papules, which were confined to the injection site and were typically palpable, asymptomatic, and non-visible. Visible nodules, with or without inflammation or dyspigmentation, have also been reported. Other adverse events include immediate and transient injection-related events such as bleeding from the injection site, discomfort, erythema or inflammation, ecchymosis, and edema.

For more information, please see Full Product Information for Sculptra®