SALT LAKE CITY, UTAH, APRIL 19, 2007

ZARS, Inc. announced today that the Medical Products Agency in Sweden has approved Rapydan™ 70 mg/70 mg medicated plaster, a topical local anesthetic patch. This action represents the first European approval for one of the companys products. Rapydan is the product known as Synera in the United States and was approved by the U.S. Food and Drug Administration (FDA) in 2005. Rapydan™ is a topical local anesthetic patch approved in Sweden for use on normal intact skin to provide surface anesthesia of the skin for needle puncture and for superficial surgical procedures in adults and for needle puncture in children 3 years and above.

ZARS has entered into a license agreement with EUSA Pharma for Rapydan™. EUSA Pharma is a pan-European specialty pharmaceutical company primarily focused in commercializing novel pain, oncology and critical care products. The agreement provides EUSA Pharma with exclusive marketing rights in Europe for the product, which is expected to be commercially available in Sweden mid-year and in additional European countries later in the year, pending additional regulatory approvals. Under the terms of the agreement, ZARS is eligible to receive milestone payments and a royalty on product sales.

"Given their focus in pain, oncology and critical care, we believe EUSA Pharma will be an excellent commercial partner for Rapydan™ in Europe," stated Robert Lippert, President and CEO of ZARS. "Rapydan™ may offer several potential benefits to patients because we believe that it is more convenient and has faster onset than other approved products."

Bryan Morton, chief executive of EUSA Pharma said "Rapydan™ will be an important focus of our sales and marketing teams and we look forward to the upcoming launch."

Rapydan™ is the first product approved in Europe using ZARS patented Controlled Heat-Assisted Drug Delivery, or CHADD, technology. Rapydan™ is comprised of a thin layer of a patented local anesthetic formulation integrated with an oxygen activated CHADD heating component. When removed from the storage pouch, Rapydan™ begins to heat, warming the skin upon application. The heating component is intended to enhance the delivery of the local anesthetics into the skin.

Rapydan™ is applied to intact skin for 30 minutes prior to needle puncture or superficial surgical procedures. In clinical trials, the most common side effect was local skin reactions, such as erythema, edema and blanching. Rapydan™ should not be used for a longer duration than recommended, and is contraindicated in patients with a known history of sensitivity to lidocaine, tetracaine or local anesthetics of the amide or ester type.

ZARS is a pharmaceutical company focused on the development and commercialization of unique products in pain management and dermatology utilizing its proprietary platform technologies. For more information regarding ZARS, please see www.zars.com.

This press release contains forward-looking statements that involve risks and uncertainties, including statements relating to potential regulatory approvals, the payment of milestones and royalties and the commercial potential of Rapydan™. Actual events could differ materially from those projected and the Company cautions readers not to place undue reliance on the forward-looking statements contained in this release.

Contacts:
Gregory S. Ayers
Chief Financial Officer
Tel: 801-350-0202