[Congressional Bills 116th Congress]
[From the U.S. Government Publishing Office]
[H.R. 2587 Introduced in House (IH)]
<DOC>
116th CONGRESS
1st Session
H. R. 2587
To require the Commissioner of Food and Drugs to develop standards for
a ``Reef Safe'' label for sunscreen.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
May 8, 2019
Ms. Gabbard (for herself and Mr. Ryan) introduced the following bill;
which was referred to the Committee on Energy and Commerce
_______________________________________________________________________
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 Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Reef Safe Act of 2019''.
SEC. 2. LABELING CRITERIA FOR ``REEF SAFE'' SUNSCREEN.
(a) In General.--As soon as practicable, but not later than 2 years
after the date of enactment of this Act, the Secretary, acting through
the Commissioner, shall develop labeling criteria for a ``Reef Safe''
designation for nonprescription sunscreen, in consultation with the
Administrator of the Environmental Protection Agency and the
Administrator of the National Oceanic and Atmospheric Administration.
(b) Reef Safe Label.--
(1) In general.--Not later than 2 years after the date of
enactment of this Act, the Secretary, acting through the
Commissioner, shall develop standards for use of the term
``Reef Safe'' on the labeling of nonprescription sunscreen,
which shall conform with the requirements of section 502 of the
Federal Food, Drug, and Cosmetic Act (21 U.S.C. 352).
(2) Criteria and consultation.--In developing the standards
described in paragraph (1), the Secretary shall--
(A) consider the impacts of active sunscreen
ingredients on the mortality of, and developmental or
reproductive disruptions to, certain marine species,
including fish, fish larvae, sea urchins, coral, and
shrimp; and
(B) consult with appropriate heads of Federal
agencies, including the Administrator of the
Environmental Protection Agency and the Administrator
of the National Oceanic and Atmospheric Administration,
with respect to studies on the impacts of active
sunscreen ingredients on living components of coral
reef ecosystems.
(c) Review and Revision.--Not less frequently than once every 10
years, the Secretary, acting through the Commissioner and in
consultation with the Administrator of the Environmental Protection
Agency and the Administrator of the National Oceanic and Atmospheric
Administration, and taking into consideration scientific studies of the
Food and Drug Administration, the Environmental Protection Agency, and
the National Oceanic and Environmental Protection Agency, shall--
(1) review the labeling standards in effect under
subsection (b)(1);
(2) if appropriate, revise the criteria under subsection
(b)(2); and
(3) in accordance with such criteria, as revised under
paragraph (2) as applicable, update the labeling standards
under subsection (b)(1).
(d) Definitions.--In this section--
(1) the terms ``active sunscreen ingredient'',
``nonprescription'', and ``sunscreen'' have the meanings given
such terms in section 586 of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 360fff);
(2) the terms ``coral'' and ``coral reef ecosystem'' have
the meanings given such terms in section 210 of the Coral Reef
Conservation Act of 2000 (16 U.S.C. 6409);
(3) the term ``Commissioner'' means the Commissioner of
Food and Drugs; and
(4) the term ``Secretary'', unless specified otherwise,
means the Secretary of Health and Human Services.
<all>