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I
116TH CONGRESS
2D SESSION
H. R. 6044
To amend the Fair Packaging and Labeling Act to require that Federal
and State mandated information declarations and labeling requirements
applicable to the chemical composition of, and radiation emitted by,
consumer products meet minimum scientific standards to deliver accurate
and clear information, and for other purposes.
IN THE HOUSE OF REPRESENTATIVES
MARCH 2, 2020
Mr. KINZINGER (for himself and Mr. SCHRADER) introduced the following bill;
which was referred to the Committee on Energy and Commerce
A BILL
To amend the Fair Packaging and Labeling Act to require
that Federal and State mandated information declara-
tions and labeling requirements applicable to the chem-
ical composition of, and radiation emitted by, consumer
products meet minimum scientific standards to deliver
accurate and clear information, and for other purposes.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
3
This Act may be cited as the ‘‘Accurate Labels Act’’.
4
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•HR 6044 IH
SEC. 2. STANDARD FOR PRODUCT LABELING INFORMATION
1
REGARDING CHEMICAL COMPOSITION AND
2
RADIATION.
3
(a) IN GENERAL.—The Fair Packaging and Labeling
4
Act (15 U.S.C. 1451 et seq.) is amended by adding at
5
the end the following:
6
‘‘SEC. 14. STANDARD FOR PRODUCT LABELING INFORMA-
7
TION REGARDING CHEMICAL COMPOSITION
8
AND RADIATION.
9
‘‘(a) DEFINITIONS.—In this section:
10
‘‘(1) BEST
AVAILABLE
SCIENCE.—The term
11
‘best available science’ means science—
12
‘‘(A) that is conducted in accordance with
13
sound and objective scientific practices;
14
‘‘(B) the findings and underlying data of
15
which are—
16
‘‘(i) reliable; and
17
‘‘(ii) if available, peer-reviewed; and
18
‘‘(C) that uses data that is collected by—
19
‘‘(i) an accepted method; or
20
‘‘(ii) the best available method if the
21
reliability of the method and the nature of
22
the decision to which the method applies
23
justifies the use of the data.
24
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‘‘(2) CONSTITUENT.—The term ‘constituent’
1
means any organic or inorganic chemical substance
2
of a particular molecular identity.
3
‘‘(3) CONSUMER
PRODUCT.—The term ‘con-
4
sumer product’ has the meaning given the term in
5
section 3(a) of the Consumer Product Safety Act
6
(15 U.S.C. 2052(a)).
7
‘‘(4) COVERED DECLARATION REQUIREMENT.—
8
The term ‘covered declaration requirement’ means a
9
legally enforceable requirement that—
10
‘‘(A) requires a responsible person to dis-
11
play or communicate covered information to a
12
consumer; and
13
‘‘(B) may be provided through—
14
‘‘(i) a statement;
15
‘‘(ii) a notice;
16
‘‘(iii) a caution;
17
‘‘(iv) a warning;
18
‘‘(v) a symbol;
19
‘‘(vi) a pictogram;
20
‘‘(vii) a vignette;
21
‘‘(viii) packaging information;
22
‘‘(ix) an insert;
23
‘‘(x) a sign;
24
‘‘(xi) a pamphlet;
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‘‘(xii) an instruction;
1
‘‘(xiii) a list of ingredients;
2
‘‘(xiv) ingredient declaration informa-
3
tion;
4
‘‘(xv) a database;
5
‘‘(xvi) an internet website; or
6
‘‘(xvii) other media, including social
7
media.
8
‘‘(5) COVERED INFORMATION.—
9
‘‘(A) IN GENERAL.—The term ‘covered in-
10
formation’ means information that—
11
‘‘(i) relates to—
12
‘‘(I) a product constituent; or
13
‘‘(II) radiation emitted by a cov-
14
ered product; and
15
‘‘(ii) expressly or by implication con-
16
veys a claim regarding or characterizing
17
the relationship between any constituent or
18
radiation and—
19
‘‘(I) a disease;
20
‘‘(II) a toxicological endpoint; or
21
‘‘(III) a health-related condition.
22
‘‘(B) IMPLIED CLAIMS.—For the purposes
23
of subparagraph (A)(ii), an implied claim in-
24
cludes a situation in which an item described in
25
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clause (i), (v), (vi), (vii), or (xvii) of paragraph
1
(4)(B) suggests, within the context in which the
2
item is presented, that a relationship exists be-
3
tween the presence or level of a constituent in
4
a covered product, or the level of exposure to a
5
constituent, and—
6
‘‘(i) a disease;
7
‘‘(ii) a health-related condition; or
8
‘‘(iii) the likelihood of a health-related
9
condition.
10
‘‘(6) COVERED PRODUCT.—The term ‘covered
11
product’—
12
‘‘(A) means—
13
‘‘(i) a consumer product; or
14
‘‘(ii) a consumer commodity; and
15
‘‘(B) includes any packaging with respect
16
to a consumer product or consumer commodity
17
described in clause (i) and (ii) of subparagraph
18
(A), respectively.
19
‘‘(7) DE MINIMIS RISK LEVEL.—The term ‘de
20
minimis risk level’ means—
21
‘‘(A) a level of risk that is based on the
22
best available science and the weight of the evi-
23
dence;
24
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‘‘(B) with respect to a constituent or radi-
1
ation that is a carcinogen, that the level of risk
2
described in subparagraph (A)—
3
‘‘(i) is determined based on a safety
4
evaluation that includes non-linear mod-
5
eling approaches that are consistent with
6
available data and scientific understanding
7
of endogenous exposures and a mode of ac-
8
tion in lieu of, or, at a minimum, in addi-
9
tion to, a linear default method;
10
‘‘(ii) takes into consideration factors
11
that include the weight of the evidence,
12
data quality and study reliability, the na-
13
ture and severity of any health effects in-
14
volved, the size of any sensitive population
15
that is at risk with respect to the con-
16
stituent or radiation, as applicable, and the
17
kind and degree of any relevant scientific
18
uncertainties; and
19
‘‘(iii) after applying the principles de-
20
scribed in clauses (i) and (ii)—
21
‘‘(I) if the likely operative cancer
22
mode of action with respect to the
23
constituent or radiation supports use
24
of a linear default model, is the level
25
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•HR 6044 IH
of exposure to the constituent or radi-
1
ation every day for 70 years that
2
would result in a not greater than 1
3
in 100,000 chance of developing can-
4
cer for an individual who is exposed to
5
the constituent or radiation; and
6
‘‘(II) if the likely operative can-
7
cer mode of action with respect to the
8
constituent or radiation is non-linear,
9
is the level of exposure to the con-
10
stituent or radiation every day for 70
11
years that would result in a not great-
12
er than 1 in 1,000 chance of devel-
13
oping cancer for an individual who is
14
exposed to the constituent or radi-
15
ation; and
16
‘‘(C) with respect to a constituent or radi-
17
ation that is a systemic toxicant, including a re-
18
productive or developmental toxicant, the level
19
of exposure to the constituent or radiation, as
20
applicable, that would result in a not greater
21
than 1 in 1,000 chance of a significant adverse
22
health impact.
23
‘‘(8) NATURALLY OCCURRING.—The term ‘nat-
24
urally occurring’ means, with respect to a con-
25
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•HR 6044 IH
stituent and a covered product, that the constituent
1
occurs in—
2
‘‘(A) any plant, animal, or microorganism,
3
or any raw material or a constituent derived
4
from a plant, animal, or microorganism, that
5
composes or is a part of the covered product;
6
and
7
‘‘(B) the covered product because of—
8
‘‘(i)(I) activity that is authorized pur-
9
suant to regulation or permitting; or
10
‘‘(II) human activity; and
11
‘‘(ii) any physical processing, prepara-
12
tion, or packaging of—
13
‘‘(I) a plant, animal, or micro-
14
organism; or
15
‘‘(II) any raw material or con-
16
stituent derived from an entity de-
17
scribed in subclause (I).
18
‘‘(9) NON-FUNCTIONAL
CONSTITUENT.—The
19
term ‘non-functional constituent’ means, with re-
20
spect to a covered product, any constituent—
21
‘‘(A) that—
22
‘‘(i) is an incidental component, at in-
23
significant levels, of an ingredient of the
24
covered product;
25
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•HR 6044 IH
‘‘(ii) is, at insignificant levels, a
1
breakdown product of an ingredient of the
2
covered product;
3
‘‘(iii) is a byproduct of the manufac-
4
turing process with respect to the covered
5
product;
6
‘‘(iv) has not been intentionally added
7
as a separate substance during the manu-
8
facturing process with respect to the cov-
9
ered product; and
10
‘‘(v) serves no technical or functional
11
effect with respect to the covered product;
12
and
13
‘‘(B) the presence of which does not en-
14
danger public health.
15
‘‘(10)
PRODUCT
CONSTITUENT.—The
term
16
‘product constituent’ means a chemical or chemical
17
substance that—
18
‘‘(A) comprises a covered product (or a
19
component of, or material with respect to, a
20
covered product) in whole or part; and
21
‘‘(B) is present in a covered product as—
22
‘‘(i) part of a specified set of ingredi-
23
ents; or
24
‘‘(ii) a non-functional constituent.
25
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•HR 6044 IH
‘‘(11) RADIATION.—
1
‘‘(A) IN GENERAL.—The term ‘radiation’
2
means—
3
‘‘(i) electromagnetic radiation, includ-
4
ing the entire electromagnetic spectrum of
5
radiation of any wavelength; and
6
‘‘(ii) radiation from naturally occur-
7
ring radioactive elements, including—
8
‘‘(I) uranium, thorium, and po-
9
tassium;
10
‘‘(II) any radioactive decay prod-
11
ucts of an element described in sub-
12
clause (I), trace concentrations of
13
which may occur in materials such as
14
stone or granite; and
15
‘‘(III) any other naturally occur-
16
ring radioactive material.
17
‘‘(B) ELECTROMAGNETIC SPECTRUM.—For
18
the purposes of subparagraph (A), the electro-
19
magnetic spectrum of radiation includes gamma
20
rays, x-rays, ultraviolet rays, visible rays, infra-
21
red rays, microwaves, radiowaves, and low fre-
22
quency radiation.
23
‘‘(12) RESPONSIBLE
PERSON.—The term ‘re-
24
sponsible person’ means—
25
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‘‘(A) the manufacturer, distributor, re-
1
tailer, or packager of a covered product that is
2
subject to a covered declaration requirement;
3
and
4
‘‘(B) the supplier of any constituent, com-
5
ponent, material, chemical or chemical sub-
6
stance, food, or packaging to an entity de-
7
scribed in subparagraph (A).
8
‘‘(13)
RISK-BASED.—The
term
‘risk-based’
9
means, with respect to a covered declaration require-
10
ment or a de minimis risk level, that the require-
11
ment or risk level, as applicable, is based on—
12
‘‘(A) the likelihood and degree of injury;
13
‘‘(B) the integration and assessment of in-
14
formation, including data, regarding hazards re-
15
sulting from specific exposures of 1 or more
16
constituents in, or radiation in or emitted from,
17
a covered product; and
18
‘‘(C) the recognition of a mode of action
19
within a systematic compilation of scientific
20
data that, within a structured framework, sup-
21
ports a hypothesized, biologically plausible path-
22
way.
23
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•HR 6044 IH
‘‘(14) TRADE SECRET.—The term ‘trade secret’
1
has the meaning given the term in section 1839 of
2
title 18, United States Code.
3
‘‘(15) WEIGHT OF THE EVIDENCE.—The term
4
‘weight of the evidence’ means a systematic review
5
method, applied in a manner that is suited to the
6
nature of evidential information or the decision to
7
which the method applies, that uses a pre-estab-
8
lished protocol to—
9
‘‘(A) comprehensively, objectively, trans-
10
parently, and consistently identify and evaluate
11
each stream of evidential information, including
12
the strengths, limitations, and relevance of any
13
study that is the basis for that evidential infor-
14
mation; and
15
‘‘(B) integrate evidence as necessary and
16
appropriate based on the strengths, limitations,
17
and relevance described in subparagraph (A).
18
‘‘(b) PROHIBITION.—
19
‘‘(1) IN GENERAL.—Unless specifically author-
20
ized by a Federal statute, no department or agency
21
of the Federal Government, State, political subdivi-
22
sion of a State, or territory or possession of the
23
United States may establish or maintain a covered
24
declaration requirement unless the covered declara-
25
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•HR 6044 IH
tion requirement satisfies the standards under para-
1
graph (2).
2
‘‘(2) STANDARDS FOR COVERED DECLARATION
3
REQUIREMENTS.—
4
‘‘(A) IN GENERAL.—A covered declaration
5
requirement shall satisfy each of the following:
6
‘‘(i) The covered information to be
7
displayed or communicated—
8
‘‘(I) is clear, accurate, and not
9
misleading or deceptive to consumers
10
with respect to the product to which
11
the covered declaration requirement
12
applies; and
13
‘‘(II) is consistent with the re-
14
quirements under section 5 of the
15
Federal Trade Commission Act (15
16
U.S.C. 45).
17
‘‘(ii) The covered information to be
18
displayed or communicated is—
19
‘‘(I) risk-based; and
20
‘‘(II) based on—
21
‘‘(aa)
the
best
available
22
science; and
23
‘‘(bb) appropriate weight of
24
the evidence review.
25
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‘‘(iii) The covered declaration require-
1
ment exempts non-functional constituents.
2
‘‘(iv) The covered declaration require-
3
ment exempts naturally occurring constitu-
4
ents.
5
‘‘(v) The covered declaration require-
6
ment—
7
‘‘
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