Browse Arkansas Code titles and sections
15 U.S.C. § 1472a — Special packaging for liquid nicotine
Federal law — U.S. Code and appendices · legal_authorities
Page 1417
TITLE 15—COMMERCE AND TRADE
§ 1472a
1 Comma retained in amendment by Pub. L. 97–414.
provisions set out as a note under section 1472a of this
title] may be cited as the ‘Child Nicotine Poisoning
Prevention Act of 2015’.’’
SHORT TITLE
Pub. L. 91–601, § 1, Dec. 30, 1970, 84 Stat. 1670, provided
that:
‘‘This
Act
[enacting
this
chapter,
section
135(z)(2)(i) of Title 7, Agriculture, and sections 343(n),
352(p), and 362(f) of Title 21, Food and Drugs, amending
section 1261(p) of this title and section 353(b)(2) of Title
21, and enacting provisions set out as a note under this
section] may be cited as the ‘Poison Prevention Pack-
aging Act of 1970’.’’
TRANSFER OF FUNCTIONS
‘‘Commission’’ substituted for ‘‘Secretary’’ and ‘‘Con-
sumer Product Safety Commission’’ substituted for
‘‘Secretary of Health, Education, and Welfare’’ in par.
(1) pursuant to section 30(a) of Pub. L. 92–573, which is
classified to section 2079(a) of this title and which
transferred functions of Secretary of Health, Edu-
cation, and Welfare under this chapter to Consumer
Product Safety Commission.
§ 1472. Special packaging standards
(a) Establishment
The Commission,1 may establish in accordance
with the provisions of this Act, by regulation,
standards for the special packaging of any
household substance if it finds that—
(1) the degree or nature of the hazard to chil-
dren in the availability of such substance, by
reason of its packaging, is such that special
packaging is required to protect children from
serious personal injury or serious illness re-
sulting from handling, using, or ingesting such
substance; and
(2) the special packaging to be required by
such standard is technically feasible, prac-
ticable, and appropriate for such substance.
(b) Consideratio
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Page 1417
TITLE 15—COMMERCE AND TRADE
§ 1472a
1 Comma retained in amendment by Pub. L. 97–414.
provisions set out as a note under section 1472a of this
title] may be cited as the ‘Child Nicotine Poisoning
Prevention Act of 2015’.’’
SHORT TITLE
Pub. L. 91–601, § 1, Dec. 30, 1970, 84 Stat. 1670, provided
that:
‘‘This
Act
[enacting
this
chapter,
section
135(z)(2)(i) of Title 7, Agriculture, and sections 343(n),
352(p), and 362(f) of Title 21, Food and Drugs, amending
section 1261(p) of this title and section 353(b)(2) of Title
21, and enacting provisions set out as a note under this
section] may be cited as the ‘Poison Prevention Pack-
aging Act of 1970’.’’
TRANSFER OF FUNCTIONS
‘‘Commission’’ substituted for ‘‘Secretary’’ and ‘‘Con-
sumer Product Safety Commission’’ substituted for
‘‘Secretary of Health, Education, and Welfare’’ in par.
(1) pursuant to section 30(a) of Pub. L. 92–573, which is
classified to section 2079(a) of this title and which
transferred functions of Secretary of Health, Edu-
cation, and Welfare under this chapter to Consumer
Product Safety Commission.
§ 1472. Special packaging standards
(a) Establishment
The Commission,1 may establish in accordance
with the provisions of this Act, by regulation,
standards for the special packaging of any
household substance if it finds that—
(1) the degree or nature of the hazard to chil-
dren in the availability of such substance, by
reason of its packaging, is such that special
packaging is required to protect children from
serious personal injury or serious illness re-
sulting from handling, using, or ingesting such
substance; and
(2) the special packaging to be required by
such standard is technically feasible, prac-
ticable, and appropriate for such substance.
(b) Considerations
In establishing a standard under this section,
the Commission shall consider—
(1) the reasonableness of such standard;
(2) available scientific, medical, and engi-
neering data concerning special packaging and
concerning childhood accidental ingestions,
illness, and injury caused by household sub-
stances;
(3) the manufacturing practices of industries
affected by this Act; and
(4) the nature and use of the household sub-
stance.
(c) Publication of findings, reasons, and citation
of statutory authorizations
In carrying out this Act, the Commission shall
publish its findings, its reasons therefor, and ci-
tation of the sections of statutes which author-
ize its action.
(d) Limitation
Nothing in this Act shall authorize the Com-
mission to prescribe specific packaging designs,
product content, package quantity, or, with the
exception
of
authority
granted
in
section
1473(a)(2) of this title, labeling. In this case of a
household substance for which special packaging
is required pursuant to a regulation under this
section, the Commission may in such regulation
prohibit the packaging of such substance in
packages which it determines are unnecessarily
attractive to children.
(e) Cost-benefit analysis not required
Nothing in this Act shall be construed to re-
quire the Consumer Product Safety Commission,
in establishing a standard under this section, to
prepare a comparison of the costs that would be
incurred in complying with such standard with
the benefits of such standard.
(Pub. L. 91–601, § 3, Dec. 30, 1970, 84 Stat. 1670;
Pub. L. 92–573, § 30(a), Oct. 27, 1972, 86 Stat. 1231;
Pub. L. 97–414, § 9(k), Jan. 4, 1983, 96 Stat. 2065;
Pub. L. 110–314, title II, § 233, Aug. 14, 2008, 122
Stat. 3073.)
Editorial Notes
REFERENCES IN TEXT
For classification to the Code of ‘‘this Act’’, referred
to in text, see References in Text note set out under
section 1471 of this title.
AMENDMENTS
2008—Subsec. (e). Pub. L. 110–314 added subsec. (e).
1983—Subsec. (a). Pub. L. 97–414 struck out ‘‘, after
consultation with the technical advisory committee
provided for in section 1475 of this title’’ after ‘‘The
Commission’’.
Statutory Notes and Related Subsidiaries
TRANSFER OF FUNCTIONS
‘‘Commission’’ substituted for ‘‘Secretary’’, ‘‘it’’ sub-
stituted for ‘‘he’’, and ‘‘its’’ substituted for ‘‘his’’ wher-
ever appearing in subsecs. (a) to (d) pursuant to section
30(a) of Pub. L. 92–573, which is classified to section
2079(a) of this title and which transferred functions of
Secretary of Health, Education, and Welfare under this
chapter to Consumer Product Safety Commission.
§ 1472a. Special packaging for liquid nicotine
containers
(a) Requirement
Notwithstanding section 1261(f)(2) of this title
and section 2052(a)(5) of this title, any nicotine
provided in a liquid nicotine container sold, of-
fered for sale, manufactured for sale, distributed
in commerce, or imported into the United
States shall be packaged in accordance with the
standards provided in section 1700.15 of title 16,
Code of Federal Regulations, as determined
through testing in accordance with the method
described in section 1700.20 of title 16, Code of
Federal
Regulations,
and
any
subsequent
changes to such sections adopted by the Com-
mission.
(b) Savings clause
(1) In general
Nothing in this section shall be construed to
limit or otherwise affect the authority of the
Secretary of Health and Human Services to
regulate, issue guidance, or take action re-
garding the manufacture, marketing, sale, dis-
tribution, importation, or packaging, includ-
ing child-resistant packaging, of nicotine, liq-
uid nicotine, liquid nicotine containers, elec-
tronic cigarettes, electronic nicotine delivery
systems or other similar products that contain
or dispense liquid nicotine, or any other nico-
tine-related products, including—
Page 1418
TITLE 15—COMMERCE AND TRADE
§ 1473
(A) authority under the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 301 et
seq.) and the Family Smoking Prevention
and Tobacco Control Act (Public Law 111–31)
and the amendments made by such Act; and
(B) authority for the rulemaking entitled
‘‘Deeming Tobacco Products to Be Subject
to the Federal Food, Drug, and Cosmetic
Act, as Amended by the Family Smoking
Prevention and Tobacco Control Act; regula-
tions on the Sale and Distribution of To-
bacco Products and the Required Warning
Statements for Tobacco Products’’ (April
2014) (FDA–2014–N–0189), the rulemaking en-
titled ‘‘Nicotine Exposure Warnings and
Child-Resistant Packaging for Liquid Nico-
tine, Nicotine-Containing E-Liquid(s), and
Other
Tobacco
Products’’
(June
2015)
(FDA–2015–N–1514), and subsequent actions
by the Secretary regarding packaging of liq-
uid nicotine containers.
(2) Consultation
If the Secretary of Health and Human Serv-
ices adopts, maintains, enforces, or imposes or
continues in effect any packaging requirement
for liquid nicotine containers, including a
child-resistant packaging requirement, the
Secretary shall consult with the Commission,
taking into consideration the expertise of the
Commission in implementing and enforcing
this section and the Poison Prevention Pack-
aging Act of 1970 (15 U.S.C. 1471 et seq.).
(c) Applicability
Notwithstanding section 2052(a)(5) of this title
and section 1261(f)(2) of this title, the require-
ment of subsection (a) shall be treated as a
standard for the special packaging of a house-
hold substance established under section 3(a) of
the Poison Prevention Packaging Act of 1970 (15
U.S.C. 1472(a)).
(d) Definitions
In this section:
(1) Commission
The term ‘‘Commission’’ means the Con-
sumer Product Safety Commission.
(2) Liquid nicotine container
(A) In general
Notwithstanding section 1261(f)(2) of this
title and section 2052(a)(5) of this title, the
term ‘‘liquid nicotine container’’ means a
package (as defined in section 2 of the Poi-
son Prevention Packaging Act of 1970 (15
U.S.C. 1471))—
(i) from which nicotine in a solution or
other form is accessible through normal
and foreseeable use by a consumer; and
(ii) that is used to hold soluble nicotine
in any concentration.
(B) Exclusion
The term ‘‘liquid nicotine container’’ does
not include a sealed, pre-filled, and dispos-
able container of nicotine in a solution or
other form in which such container is in-
serted directly into an electronic cigarette,
electronic nicotine delivery system, or other
similar product, if the nicotine in the con-
tainer is inaccessible through customary or
reasonably foreseeable handling or use, in-
cluding reasonably foreseeable ingestion or
other contact by children.
(3) Nicotine
The term ‘‘nicotine’’ means any form of the
chemical nicotine, including any salt or com-
plex, regardless of whether the chemical is
naturally or synthetically derived.
(Pub. L. 114–116, § 2, Jan. 28, 2016, 130 Stat. 3.)
Editorial Notes
REFERENCES IN TEXT
The Federal Food, Drug, and Cosmetic Act, referred
to in subsec. (b)(1), is act June 25, 1938, ch. 675, 52 Stat.
1040, which is classified generally to chapter 9 (§ 301 et
seq.) of Title 21, Food and Drugs. For complete classi-
fication of this Act to the Code, see section 301 of Title
21 and Tables.
The Family Smoking Prevention and Tobacco Con-
trol Act, referred to in subsec. (b)(1), is div. A of Pub.
L. 111–31, June 22, 2009, 123 Stat. 1776. For complete
classification of this Act to the Code, see Short Title of
2009 Amendment note set out under section 301 of Title
21, Food and Drugs, and Tables.
The Poison Prevention Packaging Act of 1970, re-
ferred to in subsec. (b)(2), is Pub. L. 91–601, Dec. 30, 1970,
84 Stat. 1670, which is classified principally to this
chapter. For complete classification of this Act to the
Code, see Short Title note set out under section 1471 of
this title and Tables.
CODIFICATION
Section was enacted as part of the Child Nicotine
Poisoning Prevention Act of 2015, and not as part of the
Poison Prevention Packaging Act of 1970 which com-
prises this chapter.
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE
Pub. L. 114–116, § 3, Jan. 28, 2016, 130 Stat. 5, provided
that: ‘‘This Act [see Short Title of 2016 Amendment
note set out under section 1471 of this title] shall take
effect on the date that is 180 days after the date of the
enactment of this Act [Jan. 28, 2016].’’
§ 1473. Conventional packages, marketing
(a) Noncomplying packages for elderly or handi-
capped persons; labeling statements
For the purpose of making any household sub-
stance which is subject to a standard established
under section 1472 of this title readily available
to elderly or handicapped persons unable to use
such substance when packaged in compliance
with such standard, the manufacturer or packer,
as the case may be, may package any household
substance, subject to such a standard, in pack-
aging of a single size which does not comply
with such standard if—
(1) the manufacturer (or packer) also sup-
plies such substance in packages which com-
ply with such standard; and
(2) the packages of such substance which do
not meet such standard bear conspicuous la-
beling stating: ‘‘This package for households
without young children’’; except that the
Commission may by regulation prescribe a
substitute statement to the same effect for
packaging too small to accommodate such la-
beling.
Cross-references
Connections may be documented source relationships, shared citations or nearby passages. Each explains its basis; a connection alone does not establish applicability to your situation.
Federal law — U.S. Code and appendices · legal_authorities
For the purpose of this Act—
(1) The term “Commission” means the Consumer Product Safety Commission.
(2) The term “household substance” means any substance which is customarily produced or distributed for sale for consumption or use, or customarily stored, by individuals in or about the household and which is—
(A) a hazardous substance as that term is defined in [section 1261(f) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section1261/f&num=0&edition=prelim);
(B) a food, drug, or cosmetic as those terms are defined in [section 321 of title 21](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section321&num=0&edition=prelim); or
(C) a substance intended for use as fuel when stored in a portable container and used in the heating, cooking, or refrigeration system of a house.
(3) The term “package” means the immediate container or wrapping in which any household substance is contained for consumption, use, or storage by individuals in or about the household, and, for purposes of [section 1473(a)(2) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section1473/a/2&num=0&edition=prelim), also means any outer container or wrapping used in the retail display of any such substance to consumers. Such term does not include—
(A) any shipping container or wrapping used solely for the transportation of any household substance in bulk or in quantity to manufacturers, packers, or processors, or to wholesale or retail distributors thereof, or
(B) any shipping container or outer wrapping used by retailers to ship or deliver any household substance to consumers unless it is the only such container or wrapping.
(4) The term “special packaging” means packaging that is designed or
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 1471
Stored review status: release_metadata_unconfirmed. The source passage cites 15 U.S.C. § 1471. This identifies an authority to review, not proof of applicability.
Federal law — U.S. Code and appendices · legal_authorities
Page 1416
TITLE 15—COMMERCE AND TRADE
§ 1461
chapter 2 of this title. For complete classification of
this Act to the Code, see section 58 of this title and Ta-
bles.
The Federal Food, Drug, and Cosmetic Act, referred
to in text, is act June 25, 1938, ch. 675, 52 Stat. 1040,
which is classified generally to chapter 9 (§ 301 et seq.)
of Title 21, Food and Drugs, For complete classification
of this Act to the Code, see section 301 of Title 21 and
Tables.
The Federal Hazardous Substances Labeling Act, re-
ferred to in text, is Pub. L. 86–613, July 12, 1960, 74 Stat.
372, which is classified generally to chapter 30 (§ 1261 et
seq.) of this title. For complete classification of this
Act to the Code, see Short Title note set out under sec-
tion 1261 of this title and Tables.
§ 1461. Effect upon State law
It is hereby declared that it is the express in-
tent of Congress to supersede any and all laws of
the States or political subdivisions thereof inso-
far as they may now or hereafter provide for the
labeling of the net quantity of contents of the
package of any consumer commodity covered by
this chapter which are less stringent than or re-
quire information different from the require-
ments of section 1453 of this title or regulations
promulgated pursuant thereto.
(Pub. L. 89–755, § 12, Nov. 3, 1966, 80 Stat. 1302.)
CHAPTER
39A—SPECIAL
PACKAGING
OF
HOUSEHOLD SUBSTANCES FOR PROTEC-
TION OF CHILDREN
Sec.
1471.
Definitions.
1472.
Special packaging standards.
1472a.
Special packaging for liquid nicotine con-
tainers.
1473.
Conventional packages, marketing.
1474.
Regulations for special packaging standards.
1475.
Repealed.
1476.
Preemption of Federal standards.
1477.
Enforcement by State Attorneys General.
§ 1471. Definitions
For the purpos
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 1471
Stored review status: historical_2024_not_currentness_verified. The source passage cites 15 U.S.C. § 1471. This identifies an authority to review, not proof of applicability.
Federal law — U.S. Code and appendices · legal_authorities
**(a) Establishment** The Commission,11 Comma retained in amendment by Pub. L. 97–414. may establish in accordance with the provisions of this Act, by regulation, standards for the special packaging of any household substance if it finds that—
(1) the degree or nature of the hazard to children in the availability of such substance, by reason of its packaging, is such that special packaging is required to protect children from serious personal injury or serious illness resulting from handling, using, or ingesting such substance; and
(2) the special packaging to be required by such standard is technically feasible, practicable, and appropriate for such substance.
**(b) Considerations** In establishing a standard under this section, the Commission shall consider—
(1) the reasonableness of such standard;
(2) available scientific, medical, and engineering data concerning special packaging and concerning childhood accidental ingestions, illness, and injury caused by household substances;
(3) the manufacturing practices of industries affected by this Act; and
(4) the nature and use of the household substance.
**(c) Publication of findings, reasons, and citation of statutory authorizations** In carrying out this Act, the Commission shall publish its findings, its reasons therefor, and citation of the sections of statutes which authorize its action.
**(d) Limitation** Nothing in this Act shall authorize the Commission to prescribe specific packaging designs, product content, package quantity, or, with the exception of authority granted in [section 1473(a)(2) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section1473/a/2&num=0&edition=prelim), labeling. In this case of a household substance for which special packaging is required purs
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 1472
Stored review status: release_metadata_unconfirmed. The source passage cites 15 U.S.C. § 1472. This identifies an authority to review, not proof of applicability.
Federal law — U.S. Code and appendices · legal_authorities
Page 1417
TITLE 15—COMMERCE AND TRADE
§ 1472a
1 Comma retained in amendment by Pub. L. 97–414.
provisions set out as a note under section 1472a of this
title] may be cited as the ‘Child Nicotine Poisoning
Prevention Act of 2015’.’’
SHORT TITLE
Pub. L. 91–601, § 1, Dec. 30, 1970, 84 Stat. 1670, provided
that:
‘‘This
Act
[enacting
this
chapter,
section
135(z)(2)(i) of Title 7, Agriculture, and sections 343(n),
352(p), and 362(f) of Title 21, Food and Drugs, amending
section 1261(p) of this title and section 353(b)(2) of Title
21, and enacting provisions set out as a note under this
section] may be cited as the ‘Poison Prevention Pack-
aging Act of 1970’.’’
TRANSFER OF FUNCTIONS
‘‘Commission’’ substituted for ‘‘Secretary’’ and ‘‘Con-
sumer Product Safety Commission’’ substituted for
‘‘Secretary of Health, Education, and Welfare’’ in par.
(1) pursuant to section 30(a) of Pub. L. 92–573, which is
classified to section 2079(a) of this title and which
transferred functions of Secretary of Health, Edu-
cation, and Welfare under this chapter to Consumer
Product Safety Commission.
§ 1472. Special packaging standards
(a) Establishment
The Commission,1 may establish in accordance
with the provisions of this Act, by regulation,
standards for the special packaging of any
household substance if it finds that—
(1) the degree or nature of the hazard to chil-
dren in the availability of such substance, by
reason of its packaging, is such that special
packaging is required to protect children from
serious personal injury or serious illness re-
sulting from handling, using, or ingesting such
substance; and
(2) the special packaging to be required by
such standard is technically feasible, prac-
ticable, and appropriate for such substance.
(b) Consideratio
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 1472
Stored review status: historical_2024_not_currentness_verified. The source passage cites 15 U.S.C. § 1472. This identifies an authority to review, not proof of applicability.
Federal law — U.S. Code and appendices · legal_authorities
**(a) Requirement** Notwithstanding [section 1261(f)(2) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section1261/f/2&num=0&edition=prelim) and [section 2052(a)(5) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2052/a/5&num=0&edition=prelim), any nicotine provided in a liquid nicotine container sold, offered for sale, manufactured for sale, distributed in commerce, or imported into the United States shall be packaged in accordance with the standards provided in section 1700.15 of title 16, Code of Federal Regulations, as determined through testing in accordance with the method described in section 1700.20 of title 16, Code of Federal Regulations, and any subsequent changes to such sections adopted by the Commission.
**(b) Savings clause**
(1) **In general** — Nothing in this section shall be construed to limit or otherwise affect the authority of the Secretary of Health and Human Services to regulate, issue guidance, or take action regarding the manufacture, marketing, sale, distribution, importation, or packaging, including child-resistant packaging, of nicotine, liquid nicotine, liquid nicotine containers, electronic cigarettes, electronic nicotine delivery systems or other similar products that contain or dispense liquid nicotine, or any other nicotine-related products, including—
(A) authority under the Federal Food, Drug, and Cosmetic Act ([21 U.S.C. 301](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title21-section301&num=0&edition=prelim) et seq.) and the Family Smoking Prevention and Tobacco Control Act (Public Law 111–31) and the amendments made by such Act; and
(B) authority for the rulemaking entitled “Deeming Tobacco Products to Be Subject to the Federal
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 1472a
Stored review status: release_metadata_unconfirmed. Same stored citation; legal effect and authority still require review.
Federal law — U.S. Code and appendices · legal_authorities
This chapter may be cited as the Federal Food, Drug, and Cosmetic Act.
Source: Supplied U.S. Code snapshot — release unconfirmed · 21 U.S.C. § 301
Stored review status: release_metadata_unconfirmed. The source passage cites 21 U.S.C. § 301. This identifies an authority to review, not proof of applicability.
Federal law — U.S. Code and appendices · legal_authorities
Page 30
TITLE 21—FOOD AND DRUGS
§ 301
Sec.
398.
Notices to States regarding imported food.
399.
Grants to enhance food safety.
399a.
Office of the Chief Scientist.
399b.
Office of Women’s Health.
399c.
Improving the training of State, local, terri-
torial, and tribal food safety officials.
399d.
Employee protections.
399e.
Nanotechnology.
399f.
Ensuring
adequate
information
regarding
pharmaceuticals for all populations, par-
ticularly underrepresented subpopulations,
including racial subgroups.
399g.
Food and Drug Administration Intercenter
Institutes.
399h.
National Centers of Excellence in Advanced
and Continuous Pharmaceutical Manufac-
turing.
399i.
Food and Drug Administration Working Cap-
ital Fund.
SUBCHAPTER I—SHORT TITLE
§ 301. Short title
This chapter may be cited as the Federal
Food, Drug, and Cosmetic Act.
(June 25, 1938, ch. 675, § 1, 52 Stat. 1040.)
Statutory Notes and Related Subsidiaries
EFFECTIVE DATE; POSTPONEMENT IN CERTAIN CASES
Act June 23, 1939, ch. 242, §§ 1, 2, 53 Stat. 853, 854, pro-
vided that:
‘‘[SEC. 1] (a) The effective date of the following provi-
sions of the Federal Food, Drug, and Cosmetic Act is
hereby postponed until January 1, 1940: Sections 402(c)
[342(c) of this title]; 403(e)(1) [343(e)(1) of this title];
403(g), (h), (i), (j), and (k) [343(g) to (k) of this title];
501(a), (4) [351(a)(4) of this title]; 502(b), (d), (e), (f), (g),
and (h) [352(b), (d) to (h) of this title]; 601(e) [361(e) of
this title]; and 602(b) [362(b) of this title].
‘‘(b) The Secretary of Agriculture shall promulgate
regulations further postponing to July 1, 1940[,] the ef-
fective date of the provisions of sections 403(e)(1)
[343(e)(1) of this title]; 403(g), (h), (i), (j), and (k) [343(g)
to (k)]; 502(b), (d), (
Source: Supplied 2024 U.S. Code historical extraction · 21 U.S.C. § 301
Stored review status: historical_2024_not_currentness_verified. The source passage cites 21 U.S.C. § 301. This identifies an authority to review, not proof of applicability.