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<bill bill-stage="Introduced-in-Senate" dms-id="A1" public-private="public" slc-id="S1-ELT22286-9R1-XJ-JLD"><metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
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<dc:title>117 S4262 IS: Formula Act of 2022</dc:title>
<dc:publisher>U.S. Senate</dc:publisher>
<dc:date>2022-05-19</dc:date>
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<dc:language>EN</dc:language>
<dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
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<distribution-code display="yes">II</distribution-code><congress>117th CONGRESS</congress><session>2d Session</session><legis-num>S. 4262</legis-num><current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber><action><action-date date="20220519" legis-day="20220517">May 19 (legislative day, May 17), 2022</action-date><action-desc><sponsor name-id="S346">Mr. Lee</sponsor> introduced the following bill; which was read twice and referred to the <committee-name committee-id="SSHR00">Committee on Health, Education, Labor, and Pensions</committee-name></action-desc></action><legis-type>A BILL</legis-type><official-title>To temporarily allow the importation of infant formula free of duty and
free of quantitative limitation, and for other purposes.</official-title></form><legis-body><section id="S1" section-type="section-one"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote><short-title>Formula Act of 2022</short-title></quote>.</text></section><section section-type="subsequent-section" id="idF085CCD3D0374BA0A36257ED76E27A92"><enum>2.</enum><header>Increasing the supply of infant formula</header><subsection id="idC2E61A2B4ECE4121920D8BDA1B427CCA"><enum>(a)</enum><header>In general</header><text display-inline="yes-display-inline">During the 180 day period beginning on the date of the enactment of this Act, infant formula classified under heading 1901.10 of the Harmonized Tariff Schedule of the United States shall enter the United States free of duty and free of quantitative limitation, if such formula—</text><paragraph id="id0F24A56065DF407B93CA645EB681187F"><enum>(1)</enum><text display-inline="yes-display-inline">is imported from a country on the list published by the Secretary of Health and Human Services under subsection (c)(1) or a member country of the European Union; and </text></paragraph><paragraph id="id71E8DF9D8B6549E48A25A1FB0D4139CC"><enum>(2)</enum><text display-inline="yes-display-inline">is lawfully marketed in the country of origin.</text></paragraph></subsection><subsection id="idaa318dafcc3c460aabc2178b946b17d3"><enum>(b)</enum><header>Guidance</header><paragraph id="id5C91BAFF9052438F85FB5EF9A0299173"><enum>(1)</enum><header>In general</header><text>The Secretary of Health and Human Services (referred to in this subsection and in subsection (c) as the <quote>Secretary</quote>) shall, not later than 7 days after the date of enactment of this Act, issue, and periodically update, as appropriate, guidance for domestic and foreign manufacturers of infant formula in order to increase availability of such formula in the United States that is safe and nutritionally adequate. </text></paragraph><paragraph id="id80de733ee72741e98c088e3bd4593e4f"><enum>(2)</enum><header>Elements of the guidance</header><text>The guidance under paragraph (1) shall address the following:</text><subparagraph id="id99895D03625A4937AEFE607C16ED4A9D"><enum>(A)</enum><text>Information to be submitted to the Secretary by foreign and domestic manufacturers of infant formula for consideration with regard to the introduction into interstate commerce (including importation) of infant formula that is safe and nutritionally adequate but that may not comply with all applicable statutory and regulatory requirements. Such information shall include—</text><clause id="iddff6b1d514b34e01adfc4a675713eba8"><enum>(i)</enum><text>safety and nutritional adequacy of the infant formula;</text></clause><clause id="id461a694ad6d442b09115a4e10456464c"><enum>(ii)</enum><text>product identification information;</text></clause><clause id="id9ab247f1f1c04160969ec0407f872a22"><enum>(iii)</enum><text>the quantity of the infant formula intended for introduction into interstate commerce;</text></clause><clause id="idca3e1215141f47caab8f0316ff4910f9"><enum>(iv)</enum><text>a copy of the label for the infant formula (with information on any allergens present on the product label and adequate instructions for safe product preparation and use) and description of the packaging of the infant formula; and</text></clause><clause id="id24db95c7cdfb4dd186c4e8504f5748d5"><enum>(v)</enum><text>manufacturing information, including test results, and facility compliance and inspection history.</text></clause></subparagraph><subparagraph id="idbdc6739ca5054713a34f36b5606b64db"><enum>(B)</enum><text>Information for manufacturers planning to increase domestic production of infant formula for purposes of addressing the ongoing shortage. </text></subparagraph></paragraph><paragraph id="id01236071C4194AA0B70EEF15CAA7FBD1"><enum>(3)</enum><header>Priority</header><text>The guidance under paragraph (1) shall provide for priority consideration for manufacturers that are able to produce large volumes of such infant formula quickly. </text></paragraph></subsection><subsection id="idEC46B4746E01426CAEA733A2305D324B"><enum>(c)</enum><header>Importation from countries meeting certain standards</header><paragraph id="idAA3D280671DA4CA7B74A4D10A1C5AAC8"><enum>(1)</enum><header>In general</header><text>Not later than 7 days after the date of enactment of this Act, the Secretary shall publish a list of countries the Secretary determines to have manufacturing and safety standards for infant formula that are similar, equivalent, or otherwise suitable, as compared to United States standards.</text></paragraph><paragraph id="id7B28AF4B5E084F91B42187FA207354A1"><enum>(2)</enum><header>Personal and commercial importation</header><text>Beginning on the date on which the list of countries is published under paragraph (1), for a period not to exceed 180 days, the Secretary shall allow personal and commercial importation of infant formula from any country on such list, as well as from any member country of the European Union, without regard to the guidance under subsection (b)(2) and the requirements of section 412 of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/350a">21 U.S.C. 350a</external-xref>), section 415 of such Act (<external-xref legal-doc="usc" parsable-cite="usc/21/350d">21 U.S.C. 350d</external-xref>), and parts 106 and 107 of title 21, Code of Federal Regulations.</text></paragraph></subsection><subsection id="id4E08743FF29E4AC89776E8D37B64D870"><enum>(d)</enum><header>Definition</header><text>In this section, the term <term>infant formula</term> has the meaning given such term in section 201(z) of the Federal Food, Drug, and Cosmetic Act (<external-xref legal-doc="usc" parsable-cite="usc/21/321">21 U.S.C. 321(z)</external-xref>). </text></subsection></section><section id="idC26AD12D51B844F58F9856919235FD22"><enum>3.</enum><header>Special supplemental nutrition program for women, infants, and children</header><subsection id="idC5C78436C6C0439E8473023F5BCD4A32"><enum>(a)</enum><header>Access for WIC beneficiaries</header><text>Notwithstanding any other provision of law, any infant formula (as defined in section 2(d)) imported into the United States pursuant to section 2(c)(2) is eligible for purchase using benefits received under the special supplemental nutrition program for women, infants, and children established by section 17 of the Child Nutrition Act of 1966 (<external-xref legal-doc="usc" parsable-cite="usc/42/1786">42 U.S.C. 1786</external-xref>).</text></subsection><subsection display-inline="no-display-inline" commented="no" id="idE7A270343F0148C4A62AD19482E02E81"><enum>(b)</enum><header>Product recalls and supply chain disruptions</header><text>Section 17 of the Child Nutrition Act of 1966 (<external-xref legal-doc="usc" parsable-cite="usc/42/1786">42 U.S.C. 1786</external-xref>) is amended—</text><paragraph id="id26a38ca19d824c84863bb3de2cb72716"><enum>(1)</enum><text>in subsection (b), by adding at the end the following:</text><quoted-block style="OLC" display-inline="no-display-inline" id="id349329e055974237a4297726ed475d82"><paragraph id="idebefa6faefc54531b491d08cafc7d439"><enum>(24)</enum><header>Supply chain disruption</header><text>The term <term>supply chain disruption</term> means a shortage of supplemental foods that impedes the redemption of food instruments, as determined by the Secretary.</text></paragraph><after-quoted-block>; and</after-quoted-block></quoted-block></paragraph><paragraph id="ida75d85d1a66e4eb0868c71d61b919fc8"><enum>(2)</enum><text>by adding at the end the following:</text><quoted-block style="OLC" display-inline="no-display-inline" id="id8c891972e62b48f6a04b1e705eeb0161"><subsection id="id2fda18e9742c45f2b560f9e25a2dd5d6"><enum>(r)</enum><header>Product recalls and supply chain disruptions</header><paragraph id="ida782f3085c8a4f3090ade68eb3f5ed09"><enum>(1)</enum><header>Definition of qualified administrative requirement</header><text>In this subsection, the term <term>qualified administrative requirement</term> means—</text><subparagraph id="id1277ff16aea341bca6e13dea0baaca54"><enum>(A)</enum><text>a requirement under this section; and</text></subparagraph><subparagraph id="idf16ac29178bf4a9483197fea9f3b3a8b"><enum>(B)</enum><text>any regulatory requirement promulgated pursuant to this section.</text></subparagraph></paragraph><paragraph id="id2723289e6d7a4a428203b358663e82d5"><enum>(2)</enum><header>Modification or waiver of requirements</header><text>Notwithstanding any other provision of law, the Secretary shall modify or waive a qualified administrative requirement to allow 1 or more State agencies—</text><subparagraph id="ide22bf336d5d7407f916d2b4ac36c87a1"><enum>(A)</enum><text>to permit vendors authorized to participate in the program under this section to exchange or substitute authorized supplemental foods obtained with food instruments with food items that are not identical (including in brand and size);</text></subparagraph><subparagraph id="idff2a4424326e49a5b4d2e68666c1db51"><enum>(B)</enum><text>to modify or waive any requirement with respect to medical documentation for the issuance of noncontract brand infant formula, except the requirements for participants receiving Food Package III (as defined in section 246.10(e)(3) of title 7, Code of Federal Regulations (as in effect on the date of enactment of this subsection));</text></subparagraph><subparagraph id="id8917085375be4995af4505397d92062d"><enum>(C)</enum><text>to modify or waive the maximum monthly allowance for infant formula;</text></subparagraph><subparagraph id="id3849b6dbb6b24db4967277e348a8b017"><enum>(D)</enum><text>to modify or waive any additional requirement with respect to supplemental food products provided under the program under this section if the modification or waiver—</text><clause id="id5ea038c9a1e7458ca417ac881bd0bcbc"><enum>(i)</enum><text>may facilitate increased access to those products;</text></clause><clause id="ide3de2754b6664f63a23662de828178b0"><enum>(ii)</enum><text>does not substantially weaken the nutritional quality of those products; and</text></clause><clause id="id17a214971e2d4130964cdd856b492bbe"><enum>(iii)</enum><text>is in accordance with any applicable guidance or directive from the Administrator of Food and Drugs determined to be applicable by the Secretary.</text></clause></subparagraph></paragraph><paragraph id="id6d87d096e8cc4b0b8386950e5195f4a3"><enum>(3)</enum><header>Duration</header><text>A modification or waiver under paragraph (2)—</text><subparagraph id="ide5b8f77c81054a339b0cfe39ce52d02e"><enum>(A)</enum><text>shall be available for a period of not more than 180 days beginning on the date of enactment of this subsection; and</text></subparagraph><subparagraph id="id7a7b288c045e4dcfb47c48739482f841"><enum>(B)</enum><text>may be renewed, subject to the condition that the Secretary shall provide notice of the renewal not less than 15 days before the renewal shall take effect.</text></subparagraph></paragraph></subsection><after-quoted-block>.</after-quoted-block></quoted-block></paragraph></subsection></section></legis-body></bill> 

