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II
116TH CONGRESS
1ST SESSION
S. 1375
To require the Commissioner of Food and Drugs to develop standards for
a ‘‘Reef Safe’’ label for sunscreen.
IN THE SENATE OF THE UNITED STATES
MAY 8, 2019
Mr. MERKLEY introduced the following bill; which was read twice and referred
to the Committee on Commerce, Science, and Transportation
A BILL
To require the Commissioner of Food and Drugs to develop
standards for a ‘‘Reef Safe’’ label for sunscreen.
Be it enacted by the Senate and House of Representa-
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tives of the United States of America in Congress assembled,
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SECTION 1. SHORT TITLE.
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This Act may be cited as the ‘‘Reef Safe Act of
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2019’’.
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SEC. 2. LABELING CRITERIA FOR ‘‘REEF SAFE’’ SUNSCREEN.
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(a) IN GENERAL.—As soon as practicable, but not
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later than 2 years after the date of enactment of this Act,
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the Secretary, acting through the Commissioner, shall de-
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velop labeling criteria for a ‘‘Reef Safe’’ designation for
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•S 1375 IS
nonprescription sunscreen, in consultation with the Ad-
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ministrator of the Environmental Protection Agency and
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the Administrator of the National Oceanic and Atmos-
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pheric Administration.
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(b) REEF SAFE LABEL.—
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(1) IN GENERAL.—Not later than 2 years after
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the date of enactment of this Act, the Secretary, act-
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ing through the Commissioner, shall develop stand-
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ards for use of the term ‘‘Reef Safe’’ on the labeling
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of nonprescription sunscreen, which shall conform
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with the requirements of section 502 of the Federal
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Food, Drug, and Cosmetic Act (21 U.S.C. 352).
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(2) CRITERIA AND CONSULTATION.—In devel-
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oping the standards described in paragraph (1), the
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Secretary shall—
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(A) consider the impacts of active sun-
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screen ingredients on the mortality of, and de-
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velopmental or reproductive disruptions to, cer-
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tain marine species, including fish, fish larvae,
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sea urchins, coral, and shrimp; and
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(B) consult with appropriate heads of Fed-
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eral agencies, including the Administrator of
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the Environmental Protection Agency and the
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Administrator of the National Oceanic and At-
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mospheric Administration, with respect to stud-
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•S 1375 IS
ies on the impacts of active sunscreen ingredi-
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ents on living components of coral reef eco-
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systems.
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(c) REVIEW
AND REVISION.—Not less frequently
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than once every 10 years, the Secretary, acting through
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the Commissioner and in consultation with the Adminis-
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trator of the Environmental Protection Agency and the
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Administrator of the National Oceanic and Atmospheric
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Administration, and taking into consideration scientific
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studies of the Food and Drug Administration, the Envi-
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ronmental Protection Agency, and the National Oceanic
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and Environmental Protection Agency, shall—
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(1) review the labeling standards in effect under
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subsection (b)(1);
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(2) if appropriate, revise the criteria under sub-
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section (b)(2); and
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(3) in accordance with such criteria, as revised
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under paragraph (2) as applicable, update the label-
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ing standards under subsection (b)(1).
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(d) NON-PREEMPTION.—Nothing in this section shall
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be construed to prevent a State from establishing, enforc-
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ing, or maintaining a requirement with respect to labeling
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criteria for a ‘‘Reef Safe’’ designation for nonprescription
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sunscreen, provided that any such State law is at least
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as restrictive as the requirements established under this
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section.
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(e) DEFINITIONS.—In this section—
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(1) the terms ‘‘active sunscreen ingredient’’,
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‘‘nonprescription’’, and ‘‘sunscreen’’ have the mean-
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ings given such terms in section 586 of the Federal
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Food, Drug, and Cosmetic Act (21 U.S.C. 360fff);
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(2) the terms ‘‘coral’’ and ‘‘coral reef eco-
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system’’ have the meanings given such terms in sec-
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tion 210 of the Coral Reef Conservation Act of 2000
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(16 U.S.C. 6409);
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(3) the term ‘‘Commissioner’’ means the Com-
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missioner of Food and Drugs; and
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(4) the term ‘‘Secretary’’, unless specified oth-
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erwise, means the Secretary of Health and Human
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Services.
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Æ
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