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15 U.S.C. § 2057b — Banning of isopropal nitrite and other
Federal law — U.S. Code and appendices · legal_authorities
Page 1726
TITLE 15—COMMERCE AND TRADE
§ 2057b
purpose approved under the Federal Food, Drug,
and Cosmetic Act [21 U.S.C. 301 et seq.].
(c) Definitions
For purposes of this section:
(1) The term ‘‘butyl nitrite’’ includes n-butyl
nitrite, isobutyl nitrite, secondary butyl ni-
trite, tertiary butyl nitrite, and mixtures con-
taining these chemicals.
(2) The term ‘‘commercial purpose’’ means
any commercial purpose other than for the
production of consumer products containing
butyl nitrite that may be used for inhaling or
otherwise introducing butyl nitrite into the
human body for euphoric or physical effects.
(d) Effective date
This section shall take effect 90 days after No-
vember 18, 1988.
(Pub. L. 100–690, title II, § 2404, Nov. 18, 1988, 102
Stat. 4231.)
Editorial Notes
REFERENCES IN TEXT
The Federal Food, Drug, and Cosmetic Act, referred
to in subsec. (b), 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.
CODIFICATION
Section was enacted as part of the Anti-Drug Abuse
Act of 1988, and not as part of the Consumer Product
Safety Act which comprises this chapter.
§ 2057b. Banning of isopropal nitrite and other
nitrites
(a) In general
Except as provided in subsection (b), volatile
alkyl nitrite shall be considered a banned haz-
ardous product under section 2057 of this title.
(b) Lawful purposes
For the purposes of section 2057 of this title, it
shall not be unlawful for any person to manufac-
ture for sale, offer for sale, distribute in com-
merce, or import into the United States volatile
alkyl nitrites for any commercial purpose or
any other purpose approve
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 2057b
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Page 1726
TITLE 15—COMMERCE AND TRADE
§ 2057b
purpose approved under the Federal Food, Drug,
and Cosmetic Act [21 U.S.C. 301 et seq.].
(c) Definitions
For purposes of this section:
(1) The term ‘‘butyl nitrite’’ includes n-butyl
nitrite, isobutyl nitrite, secondary butyl ni-
trite, tertiary butyl nitrite, and mixtures con-
taining these chemicals.
(2) The term ‘‘commercial purpose’’ means
any commercial purpose other than for the
production of consumer products containing
butyl nitrite that may be used for inhaling or
otherwise introducing butyl nitrite into the
human body for euphoric or physical effects.
(d) Effective date
This section shall take effect 90 days after No-
vember 18, 1988.
(Pub. L. 100–690, title II, § 2404, Nov. 18, 1988, 102
Stat. 4231.)
Editorial Notes
REFERENCES IN TEXT
The Federal Food, Drug, and Cosmetic Act, referred
to in subsec. (b), 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.
CODIFICATION
Section was enacted as part of the Anti-Drug Abuse
Act of 1988, and not as part of the Consumer Product
Safety Act which comprises this chapter.
§ 2057b. Banning of isopropal nitrite and other
nitrites
(a) In general
Except as provided in subsection (b), volatile
alkyl nitrite shall be considered a banned haz-
ardous product under section 2057 of this title.
(b) Lawful purposes
For the purposes of section 2057 of this title, it
shall not be unlawful for any person to manufac-
ture for sale, offer for sale, distribute in com-
merce, or import into the United States volatile
alkyl nitrites for any commercial purpose or
any other purpose approved under the Federal
Food, Drug, and Cosmetic Act [21 U.S.C. 301 et
seq.].
(c) ‘‘Commercial purpose’’ defined
For purposes of this section, the term ‘‘com-
mercial purpose’’ means any commercial pur-
pose other than for the production of consumer
products containing volatile alkyl nitrites that
may be used for inhaling or otherwise intro-
ducing volatile alkyl nitrites into the human
body for euphoric or physical effects.
(d) Effective date
This section shall take effect 90 days after No-
vember 29, 1990.
(Pub. L. 101–647, title XXXII, § 3202, Nov. 29, 1990,
104 Stat. 4917.)
Editorial Notes
REFERENCES IN TEXT
The Federal Food, Drug, and Cosmetic Act, referred
to in subsec. (b), 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.
CODIFICATION
Section was enacted as part of the Crime Control Act
of 1990, and not as part of the Consumer Product Safety
Act which comprises this chapter.
§ 2057c. Prohibition on sale of certain products
containing specified phthalates
(a) Prohibition on the sale of certain products
containing phthalates
Beginning on the date that is 180 days after
August 14, 2008, it shall be unlawful for any per-
son to manufacture for sale, offer for sale, dis-
tribute in commerce, or import into the United
States any children’s toy or child care article
that contains concentrations of more than 0.1
percent of di-(2-ethylhexyl) phthalate (DEHP),
dibutyl phthalate (DBP), or benzyl butyl phthal-
ate (BBP).
(b) Prohibition on the sale of additional products
containing certain phthalates
(1) Interim prohibition
Beginning on the date that is 180 days after
August 14, 2008, and until a final rule is pro-
mulgated under paragraph (3), it shall be un-
lawful for any person to manufacture for sale,
offer for sale, distribute in commerce, or im-
port into the United States any children’s toy
that can be placed in a child’s mouth or child
care article that contains concentrations of
more than 0.1 percent of diisononyl phthalate
(DINP), diisodecyl phthalate (DIDP), or di-n-
octyl phthalate (DnOP).
(2) Chronic Hazard Advisory Panel
(A) Appointment
Not earlier than 180 days after August 14,
2008, the Commission shall begin the process
of appointing a Chronic Hazard Advisory
Panel pursuant to the procedures of section
28 of the Consumer Product Safety Act (15
U.S.C. 2077) to study the effects on children’s
health of all phthalates and phthalate alter-
natives as used in children’s toys and child
care articles.
(B) Examination
The panel shall, within 18 months after its
appointment under subparagraph (A), com-
plete an examination of the full range of
phthalates that are used in products for chil-
dren and shall—
(i) examine all of the potential health ef-
fects (including endocrine disrupting ef-
fects) of the full range of phthalates;
(ii) consider the potential health effects
of each of these phthalates both in isola-
tion
and
in
combination
with
other
phthalates;
(iii) examine the likely levels of chil-
dren’s, pregnant women’s, and others’ ex-
posure to phthalates, based on a reason-
able estimation of normal and foreseeable
use and abuse of such products;
(iv) consider the cumulative effect of
total exposure to phthalates, both from
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Federal law — U.S. Code and appendices · legal_authorities
**(a) In general** Except as provided in subsection (b), volatile alkyl nitrite shall be considered a banned hazardous product under [section 2057 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2057&num=0&edition=prelim).
**(b) Lawful purposes** For the purposes of [section 2057 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2057&num=0&edition=prelim), it shall not be unlawful for any person to manufacture for sale, offer for sale, distribute in commerce, or import into the United States volatile alkyl nitrites for any commercial purpose or any other purpose approved 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.].
**(c) “Commercial purpose” defined** For purposes of this section, the term “commercial purpose” means any commercial purpose other than for the production of consumer products containing volatile alkyl nitrites that may be used for inhaling or otherwise introducing volatile alkyl nitrites into the human body for euphoric or physical effects.
**(d) Effective date** This section shall take effect 90 days after November 29, 1990.
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 2057b
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
**(a) Appointment; purposes** The Commission shall appoint Chronic Hazard Advisory Panels (hereinafter referred to as the Panel or Panels) to advise the Commission in accordance with the provisions of [section 2080(b) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2080/b&num=0&edition=prelim) respecting the chronic hazards of cancer, birth defects, and gene mutations associated with consumer products.
**(b) Composition; membership** Each Panel shall consist of 7 members appointed by the Commission from a list of nominees who shall be nominated by the President of the National Academy of Sciences from scientists—
(1) who are not officers or employees of the United States (other than employees of the National Institutes of Health, the National Toxicology Program, or the National Center for Toxicological Research), and who do not receive compensation from or have any substantial financial interest in any manufacturer, distributor, or retailer of a consumer product; and
(2) who have demonstrated the ability to critically assess chronic hazards and risks to human health presented by the exposure of humans to toxic substances or as demonstrated by the exposure of animals to such substances.
The President of the National Academy of Sciences shall nominate for each Panel a number of individuals equal to three times the number of members to be appointed to the Panel.
**(c) Chairman and Vice Chairman; election; term** The Chairman and Vice Chairman of the Panel shall be elected from among the members and shall serve for the duration of the Panel.
**(d) Majority vote** Decisions of the Panel shall be made by a majority of the Panel.
**(e) Administrative support services** The Commission shall provide each Panel with such administra
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 2077
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Federal law — U.S. Code and appendices · legal_authorities
Page 1761
TITLE 15—COMMERCE AND TRADE
§ 2078
Statutory Notes and Related Subsidiaries
DEFINITIONS
For definitions of ‘‘Commission’’ and ‘‘appropriate
Congressional committees’’ used in this section, see
section 2(a) of Pub. L. 110–314, set out as a note under
section 2051 of this title.
§ 2077. Chronic Hazard Advisory Panels
(a) Appointment; purposes
The Commission shall appoint Chronic Hazard
Advisory Panels (hereinafter referred to as the
Panel or Panels) to advise the Commission in
accordance with the provisions of section 2080(b)
of this title respecting the chronic hazards of
cancer, birth defects, and gene mutations associ-
ated with consumer products.
(b) Composition; membership
Each Panel shall consist of 7 members ap-
pointed by the Commission from a list of nomi-
nees who shall be nominated by the President of
the National Academy of Sciences from sci-
entists—
(1) who are not officers or employees of the
United States (other than employees of the
National Institutes of Health, the National
Toxicology Program, or the National Center
for Toxicological Research), and who do not
receive compensation from or have any sub-
stantial financial interest in any manufac-
turer, distributor, or retailer of a consumer
product; and
(2) who have demonstrated the ability to
critically assess chronic hazards and risks to
human health presented by the exposure of hu-
mans to toxic substances or as demonstrated
by the exposure of animals to such substances.
The President of the National Academy of
Sciences shall nominate for each Panel a num-
ber of individuals equal to three times the num-
ber of members to be appointed to the Panel.
(c) Chairman and Vice Chairman; election; term
The Chairman and Vice Chairman of the Panel
shall be elected from am
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 2077
Stored review status: historical_2024_not_currentness_verified. The source passage cites 15 U.S.C. § 2077. This identifies an authority to review, not proof of applicability.
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.