More Options for Infants and Parents Act of 2022
This bill requires the Food and Drug Administration (FDA) to (1) act upon any pending applications from domestic manufacturers for new infant formula within 14 days of the bill's enactment, and (2) maintain a list on its website of infant formula products that may be substituted for certain specialized infant formula products that are in shortage. It also authorizes the FDA to waive certain labeling and nutritional requirements in furtherance of other necessary infant formula product substitutions.
[Congressional Bills 117th Congress]
[From the U.S. Government Publishing Office]
[H.R. 8010 Introduced in House (IH)]
<DOC>
117th CONGRESS
2d Session
H. R. 8010
To require the Secretary of Health and Human Services, acting through
the Commissioner of Food and Drugs, to act upon pending submissions for
new infant formula, to increase regulatory flexibility in the event of
an infant formula shortage, and for other purposes.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
June 9, 2022
Mr. Guthrie (for himself, Mr. Griffith, Mr. McKinley, Mr. Armstrong,
Mr. Joyce of Pennsylvania, Mr. Bucshon, Mr. Dunn, Mr. Carter of
Georgia, and Mr. Bilirakis) introduced the following bill; which was
referred to the Committee on Energy and Commerce
_______________________________________________________________________
A BILL
To require the Secretary of Health and Human Services, acting through
the Commissioner of Food and Drugs, to act upon pending submissions for
new infant formula, to increase regulatory flexibility in the event of
an infant formula shortage, and for other purposes.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``More Options for Infants and Parents
Act of 2022''.
SEC. 2. PENDING SUBMISSIONS FOR NEW INFANT FORMULA.
Not later than 14 days after the date of enactment of this Act, the
Secretary of Health and Human Services, acting through the Commissioner
of Food and Drugs, shall act upon any pending submissions from domestic
manufacturers for new infant formula under section 412(c) of the
Federal Food, Drug, and Cosmetic Act (21 U.S.C. 350a(c)).
SEC. 3. REGULATORY FLEXIBILITY IN THE EVENT OF AN INFANT FORMULA
SHORTAGE.
Section 412 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C.
350a) is amended by adding at the end the following:
``(j) Regulatory Flexibility in the Event of a Shortage.--
``(1) List of products for substitution during a
shortage.--The Secretary shall publish and keep up-to-date a
list on the internet website of the Food and Drug
Administration detailing which infant formula products may be
appropriate substitutes for infant formula products--
``(A) which the Secretary has determined to be in
shortage or at risk of being in shortage; and
``(B) that are relied upon by infants and
individuals with amino-acid and metabolic conditions.
``(2) Flexibilities.--The Secretary--
``(A) shall consider whether any infant formula
products may be substituted for those in shortage; and
``(B) may waive any applicable requirements under
section 412 of the Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 350a) regarding labeling and nutrient
content to facilitate such substitutions.''.
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Introduced in House
Introduced in House
Referred to the House Committee on Energy and Commerce.
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