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15 U.S.C. § 2057c — Prohibition on sale of certain products containing specified phthalates
Federal law — U.S. Code and appendices · legal_authorities
**(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 person to manufacture for sale, offer for sale, distribute 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 phthalate (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 promulgated under paragraph (3), it shall be unlawful for any person to manufacture for sale, offer for sale, distribute in commerce, or import 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](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2077&num=0&edition=prelim)) to study the effects on children’s health of all phthalates and phthalate alternatives as used in children’s toys and child care articles.
(B) *Examination* — The panel shall, within 18 months after its appointment under subparagraph (A), complete an examination of the full range of phthalates that are used in products for children and shall
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Source file: Laws/federal/codes/united-states-code/title-15/section-2057c-prohibition-on-sale-of-certain-products-containing-specified-phthalates--5ab07a9cf2.md
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Source location: Title 15, Chapter 47, § 2057c; chapter-047-consumer-product-safety.md
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**(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 person to manufacture for sale, offer for sale, distribute 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 phthalate (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 promulgated under paragraph (3), it shall be unlawful for any person to manufacture for sale, offer for sale, distribute in commerce, or import 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](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2077&num=0&edition=prelim)) to study the effects on children’s health of all phthalates and phthalate alternatives as used in children’s toys and child care articles.
(B) *Examination* — The panel shall, within 18 months after its appointment under subparagraph (A), complete an examination of the full range of phthalates that are used in products for children and shall—
(i) examine all of the potential health effects (including endocrine disrupting effects) of the full range of phthalates;
(ii) consider the potential health effects of each of these phthalates both in isolation and in combination with other phthalates;
(iii) examine the likely levels of children’s, pregnant women’s, and others’ exposure to phthalates, based on a reasonable estimation of normal and foreseeable use and abuse of such products;
(iv) consider the cumulative effect of total exposure to phthalates, both from children’s products and from other sources, such as personal care products;
(v) review all relevant data, including the most recent, best-available, peer-reviewed, scientific studies of these phthalates and phthalate alternatives that employ objective data collection practices or employ other objective methods;
(vi) consider the health effects of phthalates not only from ingestion but also as a result of dermal, hand-to-mouth, or other exposure;
(vii) consider the level at which there is a reasonable certainty of no harm to children, pregnant women, or other susceptible individuals and their offspring, considering the best available science, and using sufficient safety factors to account for uncertainties regarding exposure and susceptibility of children, pregnant women, and other potentially susceptible individuals; and
(viii) consider possible similar health effects of phthalate alternatives used in children’s toys and child care articles.
The panel’s examinations pursuant to this paragraph shall be conducted de novo. The findings and conclusions of any previous Chronic Hazard Advisory Panel on this issue and other studies conducted by the Commission shall be reviewed by the panel but shall not be considered determinative.
(C) *Report* — Not later than 180 days after completing its examination, the panel appointed under subparagraph (A) shall report to the Commission the results of the examination conducted under this section and shall make recommendations to the Commission regarding any phthalates (or combinations of phthalates) in addition to those identified in subsection (a) or phthalate alternatives that the panel determines should be declared banned hazardous substances.
(3) **Permanent prohibition by rule** — Not later than 180 days after receiving the report of the panel under paragraph (2)(C), the Commission shall, pursuant to [section 553 of title 5](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title5-section553&num=0&edition=prelim), promulgate a final rule to—
(A) determine, based on such report, whether to continue in effect the prohibition under paragraph (1), in order to ensure a reasonable certainty of no harm to children, pregnant women, or other susceptible individuals with an adequate margin of safety; and
(B) evaluate the findings and recommendations of the Chronic Hazard Advisory Panel and declare any children’s product containing any phthalates to be a banned hazardous product under section 8 of the Consumer Product Safety Act ([15 U.S.C. 2057](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2057&num=0&edition=prelim)), as the Commission determines necessary to protect the health of children.
**(c) Application** Effective on August 12, 2011,11 See References in Text note below. subsections (a) and (b)(1) and any rule promulgated under subsection (b)(3) shall apply to any plasticized component part of a children’s toy or child care article or any other component part of a children’s toy or child care article that is made of other materials that may contain phthalates.
**(d) Exclusion for inaccessible component parts**
(1) **In general** — The prohibitions established under subsections (a) and (b) shall not apply to any component part of a children’s toy or child care article that is not accessible to a child through normal and reasonably foreseeable use and abuse of such product, as determined by the Commission. A component part is not accessible under this paragraph if such component part is not physically exposed by reason of a sealed covering or casing and does not become physically exposed through reasonably foreseeable use and abuse of the product. Reasonably foreseeable use and abuse shall include swallowing, mouthing, breaking, or other children’s activities, and the aging of the product.
(2) **Limitation** — The Commission may revoke an exclusion or all exclusions granted under paragraph (1) at any time and require that any or all component parts manufactured after such exclusion is revoked comply with the prohibitions established under subsections (a) and (b) if the Commission finds, based on scientific evidence, that such compliance is necessary to protect the public health or safety.
(3) **Inaccessibility proceeding** — Within 1 year after August 12, 2011, the Commission shall—
(A) promulgate a rule providing guidance with respect to what product components, or classes of components, will be considered to be inaccessible for purposes of paragraph (1); or
(B) adopt the same guidance with respect to inaccessibility that was adopted by the Commission with regards to accessibility of lead under [section 1278a(b)(2)(B) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section1278a/b/2/B&num=0&edition=prelim), with additional consideration, as appropriate, of whether such component can be placed in a child’s mouth.
(4) **Application pending commission guidance** — Until the Commission promulgates a rule pursuant to paragraph (3), the determination of whether a product component is inaccessible to a child shall be made in accordance with the requirements laid out in paragraph (1) for considering a component to be inaccessible to a child.
**(e) Treatment of violation** A violation of subsection (a) or (b)(1) or any rule promulgated by the Commission under subsection (b)(3) shall be treated as a violation of section 19(a)(1) of the Consumer Product Safety Act ([15 U.S.C. 2068(a)(1)](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2068/a/1&num=0&edition=prelim)).
**(f) Treatment as consumer product safety standards; effect on State laws** Subsections (a) and (b)(1) and any rule promulgated under subsection (b)(3) shall be considered consumer product safety standards under the Consumer Product Safety Act [[15 U.S.C. 2051](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2051&num=0&edition=prelim) et seq.]. Nothing in this section or the Consumer Product Safety Act ([15 U.S.C. 2051](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2051&num=0&edition=prelim) et seq.) shall be construed to preempt or otherwise affect any State requirement with respect to any phthalate alternative not specifically regulated in a consumer product safety standard under the Consumer Product Safety Act.
**(g) Definitions**
(1) **Defined terms** — As used in this section:
(A) The term “phthalate alternative” means any common substitute to a phthalate, alternative material to a phthalate, or alternative plasticizer.
(B) The term “children’s toy” means a consumer product designed or intended by the manufacturer for a child 12 years of age or younger for use by the child when the child plays.
(C) The term “child care article” means a consumer product designed or intended by the manufacturer to facilitate sleep or the feeding of children age 3 and younger, or to help such children with sucking or teething.
(D) The term “consumer product” has the meaning given such term in section 3(a)(1) of the Consumer Product Safety Act ([15 U.S.C. 2052(a)(1)](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2052/a/1&num=0&edition=prelim)).
(2) **Determination guidelines**
(A) *Age* — In determining whether products described in paragraph (1) are designed or intended for use by a child of the ages specified, the following factors shall be considered:
(i) A statement by a manufacturer about the intended use of such product, including a label on such product if such statement is reasonable.
(ii) Whether the product is represented in its packaging, display, promotion, or advertising as appropriate for use by children of the ages specified.
(iii) Whether the product is commonly recognized by consumers as being intended for use by a child of the ages specified.
(iv) The Age Determination guidelines issued by the Commission staff in September 2002 and any successor to such guidelines.
(B) *Toy that can be placed in a child’s mouth* — For purposes of this section a toy can be placed in a child’s mouth if any part of the toy can actually be brought to the mouth and kept in the mouth by a child so that it can be sucked and chewed. If the children’s product can only be licked, it is not regarded as able to be placed in the mouth. If a toy or part of a toy in one dimension is smaller than 5 centimeters, it can be placed in the mouth.
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Federal law — U.S. Code and appendices · legal_authorities
Whenever the Commission finds that—
(1) a consumer product is being, or will be, distributed in commerce and such consumer product presents an unreasonable risk of injury; and
(2) no feasible consumer product safety standard under this chapter would adequately protect the public from the unreasonable risk of injury associated with such product,
the Commission may, in accordance with [section 2058 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2058&num=0&edition=prelim), promulgate a rule declaring such product a banned hazardous product.
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 2057
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Federal law — U.S. Code and appendices · legal_authorities
**(a)** The Congress finds that—
(1) an unacceptable number of consumer products which present unreasonable risks of injury are distributed in commerce;
(2) complexities of consumer products and the diverse nature and abilities of consumers using them frequently result in an inability of users to anticipate risks and to safeguard themselves adequately;
(3) the public should be protected against unreasonable risks of injury associated with consumer products;
(4) control by State and local governments of unreasonable risks of injury associated with consumer products is inadequate and may be burdensome to manufacturers;
(5) existing Federal authority to protect consumers from exposure to consumer products presenting unreasonable risks of injury is inadequate; and
(6) regulation of consumer products the distribution or use of which affects interstate or foreign commerce is necessary to carry out this chapter.
**(b)** The purposes of this chapter are—
(1) to protect the public against unreasonable risks of injury associated with consumer products;
(2) to assist consumers in evaluating the comparative safety of consumer products;
(3) to develop uniform safety standards for consumer products and to minimize conflicting State and local regulations; and
(4) to promote research and investigation into the causes and prevention of product-related deaths, illnesses, and injuries.
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 2051
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Federal law — U.S. Code and appendices · legal_authorities
**(a)** This section applies, according to the provisions thereof, except to the extent that there is involved—
(1) a military or foreign affairs function of the United States; or
(2) a matter relating to agency management or personnel or to public property, loans, grants, benefits, or contracts.
**(b)** General notice of proposed rule making shall be published in the Federal Register, unless persons subject thereto are named and either personally served or otherwise have actual notice thereof in accordance with law. The notice shall include—
(1) a statement of the time, place, and nature of public rule making proceedings;
(2) reference to the legal authority under which the rule is proposed;
(3) either the terms or substance of the proposed rule or a description of the subjects and issues involved; and
(4) the Internet address of a summary of not more than 100 words in length of the proposed rule, in plain language, that shall be posted on the Internet website under section 206(d) of the E-Government Act of 2002 ([44 U.S.C. 3501](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title44-section3501&num=0&edition=prelim) note) (commonly known as regulations.gov).
Except when notice or hearing is required by statute, this subsection does not apply—
(A) to interpretative rules, general statements of policy, or rules of agency organization, procedure, or practice; or
(B) when the agency for good cause finds (and incorporates the finding and a brief statement of reasons therefor in the rules issued) that notice and public procedure thereon are impracticable, unnecessary, or contrary to the public interest.
**(c)** After notice required by this section, the agency shall give interested persons an opportunity to participate in the rule making through subm
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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
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Federal law — U.S. Code and appendices · legal_authorities
Page 1698
TITLE 15—COMMERCE AND TRADE
§ 2051
Sec.
2056a.
Standards and consumer registration of dura-
ble nursery products.
2056b.
Mandatory toy safety standards.
2056c.
Sulfur content in drywall standard.
2056d.
Performance standards to protect against
portable fuel container explosions near
open flames or other ignition sources.
2056e.
Consumer product safety standard for button
cell or coin batteries and consumer prod-
ucts containing such batteries.
2056f.
Consumer product safety standard to protect
against tip-over of clothing storage units.
2057.
Banned hazardous products.
2057a.
Banning of butyl nitrite.
2057b.
Banning
of
isopropal
nitrite
and
other
nitrites.
2057c.
Prohibition on sale of certain products con-
taining specified phthalates.
2057d.
Banning of inclined sleepers for infants.
2057e.
Banning of crib bumpers.
2058.
Procedure for consumer product safety rules.
2059.
Repealed.
2060.
Judicial review of consumer product safety
rules.
2061.
Imminent hazards.
2062.
Repealed.
2063.
Product certification and labeling.
2064.
Substantial product hazards.
2065.
Inspection and recordkeeping.
2066.
Imported products.
2067.
Exemption of exports.
2068.
Prohibited acts.
2069.
Civil penalties.
2070.
Criminal penalties.
2071.
Injunctive enforcement and seizure.
2072.
Suits for damages.
2073.
Additional enforcement of product safety
rules and section 2064 orders.
2074.
Private remedies.
2075.
State standards.
2076.
Additional functions of Consumer Product
Safety Commission.
2076a.
Report on civil penalties.
2076b.
Inspector General audits and reports.
2077.
Chronic Hazard Advisory Panels.
2078.
Cooperation with States and other Federal
agencies.
2079.
Transfers of functions.
2080.
Limi
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 2051
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Federal law — U.S. Code and appendices · legal_authorities
**(a) In general** In this chapter:
(1) **Appropriate Congressional committees** — The term “appropriate Congressional committees” means the Committee on Energy and Commerce of the House of Representatives and the Committee on Commerce, Science, and Transportation of the Senate.
(2) **Children’s product** — The term “children’s product” means a consumer product designed or intended primarily for children 12 years of age or younger. In determining whether a consumer product is primarily intended for a child 12 years of age or younger, the following factors shall be considered:
(A) A statement by a manufacturer about the intended use of such product, including a label on such product if such statement is reasonable.
(B) Whether the product is represented in its packaging, display, promotion, or advertising as appropriate for use by children 12 years of age or younger.
(C) Whether the product is commonly recognized by consumers as being intended for use by a child 12 years of age or younger.
(D) The Age Determination Guidelines issued by the Commission staff in September 2002, and any successor to such guidelines.
(3) **Commerce** — The term “commerce” means trade, traffic, commerce, or transportation—
(A) between a place in a State and any place outside thereof, or
(B) which affects trade, traffic, commerce, or transportation described in subparagraph (A).
(4) **Commission** — The term “Commission” means the Consumer Product Safety Commission, established by [section 2053 of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2053&num=0&edition=prelim).
(5) **Consumer product** — The term “consumer product” means any article, or component part thereof, produced or distributed (i) for sale to a consumer for use in
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 2052
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Federal law — U.S. Code and appendices · legal_authorities
Page 1699
TITLE 15—COMMERCE AND TRADE
§ 2052
and Zachary Burt Memorial Carbon Monoxide Poi-
soning Prevention Act of 2022’.’’
SHORT TITLE OF 2013 AMENDMENT
Pub. L. 112–266, § 1, Jan. 14, 2013, 126 Stat. 2437, pro-
vided that: ‘‘This Act [enacting section 2056c of this
title and provisions set out as notes under section 2056c
of this title] may be cited as the ‘Drywall Safety Act
of 2012’.’’
SHORT TITLE OF 2008 AMENDMENT
Pub. L. 110–314, § 1(a), Aug. 14, 2008, 122 Stat. 3016, pro-
vided that: ‘‘This Act [enacting sections 1278a, 1477,
2053a, 2055a, 2056a, 2056b, 2057c, 2076b, 2086 to 2089, and
8008 of this title, amending sections 1191, 1193, 1194, 1196,
1201 to 1204, 1261 to 1266, 1269 to 1276, 1278, 1472, 2052,
2054, 2055, 2058, 2060, 2063 to 2070, 2073, 2076, 2077 to 2079,
2081, 2082, 8002, and 8003 of this title, enacting provi-
sions set out as notes under this section and sections
1194, 2053, 2060, 2063, 2066, 2069, and 2076 of this title,
amending provisions set out as notes under sections 401
and 1261 of this title and section 1113 of Title 31, Money
and Finance, and repealing provisions set out as a note
under section 2053 of this title] may be cited as the
‘Consumer Product Safety Improvement Act of 2008’.’’
SHORT TITLE OF 1990 AMENDMENT
Pub. L. 101–608, § 1, Nov. 16, 1990, 104 Stat. 3110, pro-
vided that: ‘‘This Act [enacting sections 2076a and 2084
of this title, amending sections 1193, 1194, 1262, 1274,
2053, 2055, 2056, 2058, 2061, 2064, 2066, 2069, 2077, and 2081
of this title, and enacting provisions set out as notes
under sections 2053, 2054, 2056, 2076, and 2084 of this
title] may be cited as the ‘Consumer Product Safety
Improvement Act of 1990’.’’
SHORT TITLE OF 1981 AMENDMENT
Pub. L. 97–35, title XII, § 1201(a), Aug. 13, 1981,
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 2052
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Federal law — U.S. Code and appendices · legal_authorities
Page 1725
TITLE 15—COMMERCE AND TRADE
§ 2057a
(e) Revision of voluntary standard
(1) Notice to commission
If the performance requirements of a vol-
untary standard adopted under subsection (d)
are subsequently revised, the organization
that revised the performance requirements of
such standard shall notify the Commission of
such revision after final approval.
(2) Treatment of revision
Not later than 90 days after the date on
which the Commission is notified of revised
performance requirements of a voluntary
standard described in paragraph (1) (or such
later date as the Commission determines ap-
propriate), the Commission shall determine
whether the revised performance requirements
meet the requirements of subsection (d)(2)(B),
and if so, modify, in accordance with section
553 of title 5, the standard promulgated under
subsection (d) to include the revised perform-
ance requirements that the Commission deter-
mines meet such requirements. The modified
standard shall take effect after 180 days or
such later date as the Commission deems ap-
propriate.
(f) Subsequent rulemaking
(1) In general
Beginning 5 years after December 29, 2022,
subsequent to the publication of a consumer
product safety standard under this section, the
Commission may, at any time, initiate rule-
making, in accordance with section 553 of title
5, to modify the requirements of such standard
or to include additional provisions if the Com-
mission makes a determination that such
modifications or additions are reasonably nec-
essary to protect children from tip-over-re-
lated death or injury.
(2) Petition for revision of rule
(A) In general
If the Commission receives a petition for a
new or revised test that permits incor-
porated safety features (excluding tip re-
straints
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 2057
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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. § 2057c
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Federal law — U.S. Code and appendices · legal_authorities
**(a) Designation** It shall be unlawful for any person to—
(1) sell, offer for sale, manufacture for sale, distribute in commerce, or import into the United States any consumer product, or other product or substance that is regulated under this chapter or any other Act enforced by the Commission, that is not in conformity with an applicable consumer product safety rule under this chapter, or any similar rule, regulation, standard, or ban under any other Act enforced by the Commission;
(2) sell, offer for sale, manufacture for sale, distribute in commerce, or import into the United States any consumer product, or other product or substance that is—
(B) 11 So in original. No subpar. (A) has been enacted. subject to voluntary corrective action taken by the manufacturer, in consultation with the Commission, of which action the Commission has notified the public or if the seller, distributor, or manufacturer knew or should have known of such voluntary corrective action;
(C) subject to an order issued under section 2061 or 2064 of this title; or
(D) a banned hazardous substance within the meaning of [section 1261(q)(1) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section1261/q/1&num=0&edition=prelim);
(3) fail or refuse to permit access to or copying of records, or fail or refuse to establish or maintain records, or fail or refuse to make reports or provide information, or fail or refuse to permit entry or inspection, as required under this chapter or rule thereunder;
(4) fail to furnish information required by [section 2064(b) of this title](https://uscode.house.gov/view.xhtml?req=granuleid:USC-prelim-title15-section2064/b&num=0&edition=prelim);
(5) fail to comply with an order issued under section 2064(c) or (d) of this
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 2068
Stored review status: release_metadata_unconfirmed. The source passage cites 15 U.S.C. § 2068. This identifies an authority to review, not proof of applicability.