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<bill bill-stage="Introduced-in-Senate" dms-id="A1" public-private="public">
	<form>
		<distribution-code display="yes">II</distribution-code>
		<congress>110th CONGRESS</congress>
		<session>2d Session</session>
		<legis-num>S. 3425</legis-num>
		<current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber>
		<action>
			<action-date date="20080801">August 1, 2008</action-date>
			<action-desc><sponsor name-id="S150">Mr. Dodd</sponsor> (for himself,
			 <cosponsor name-id="S259">Mr. Reed</cosponsor>, <cosponsor name-id="S173">Mr.
			 Kerry</cosponsor>, <cosponsor name-id="S277">Mr. Carper</cosponsor>,
			 <cosponsor name-id="S278">Mrs. Clinton</cosponsor>, and
			 <cosponsor name-id="S010">Mr. Biden</cosponsor>) introduced the following bill;
			 which was read twice and referred to the <committee-name committee-id="SSHR00">Committee on Health, Education, Labor, and
			 Pensions</committee-name></action-desc>
		</action>
		<legis-type>A BILL</legis-type>
		<official-title>To make effective the proposed rule of the Food and Drug
		  Administration relating to sunscreen drug products, and for other
		  purposes.</official-title>
	</form>
	<legis-body>
		<section id="S1" section-type="section-one"><enum>1.</enum><header>Short
			 title</header><text display-inline="no-display-inline">This Act may be cited as
			 the <quote><short-title>Sunscreen Labeling Protection Act
			 of 2008</short-title></quote> or the <quote>SUN Act</quote>.</text>
		</section><section id="idEF771AA7F6CB4228B719039D9C261C82"><enum>2.</enum><header>Effective date
			 for rule relating to sunscreen drug products for over-the-counter human
			 use</header><text display-inline="no-display-inline">Notwithstanding subchapter
			 II of chapter 5, and chapter 7, of title 5, United States Code (commonly known
			 as the <quote>Administrative Procedure Act</quote>) and any other provision of
			 law, the proposed rule issued by the Commissioner of Food and Drugs entitled
			 <quote>Sunscreen Drug Products for Over-the-Counter Human Use; Proposed
			 Amendment of Final Monograph</quote>, 72 Fed. Reg. 49070 (August 27, 2007),
			 shall take effect on the date that is 180 days after the date of enactment of
			 this Act, unless such Commissioner issues the final rule, which includes
			 formulation, labeling, and testing requirements for both ultraviolet B (UVB)
			 and ultraviolet A (UVA) radiation protection, before such effective
			 date.</text>
		</section></legis-body>
</bill>
