[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. 3122 Introduced in Senate (IS)]

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119th CONGRESS
  1st Session
                                S. 3122

     To amend the Federal Food, Drug, and Cosmetic Act to require 
   notifications to the Food and Drug Administration regarding food 
    substances generally recognized as safe, and for other purposes.


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                            November 6, 2025

   Mr. Marshall (for himself, Mrs. Britt, and Mr. Scott of Florida) 
introduced the following bill; which was read twice and referred to the 
          Committee on Health, Education, Labor, and Pensions

_______________________________________________________________________

                                 A BILL


 
     To amend the Federal Food, Drug, and Cosmetic Act to require 
   notifications to the Food and Drug Administration regarding food 
    substances generally recognized as safe, 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 ``Better Food Disclosure Act of 2025'' 
or the ``Better FDA Act of 2025''.

SEC. 2. MANDATORY REPORTING OF SUBSTANCES GENERALLY RECOGNIZED AS SAFE.

    (a) In General.--Chapter IV of the Federal Food, Drug, and Cosmetic 
Act (21 U.S.C. 341 et seq.) is amended by inserting after section 409 
the following:

``SEC. 409A. FOOD SUBSTANCES GENERALLY RECOGNIZED AS SAFE.

    ``(a) In General.--Beginning on the date that is 2 years after the 
date of enactment of the Better Food Disclosure Act of 2025, a food 
substance generally recognized as safe shall, with respect to any 
particular use or intended use, be deemed to be unsafe for the purposes 
of the application of clause (2)(C) of section 402(a), unless--
            ``(1) the Secretary includes the food substance on the list 
        described in subsection (c); or
            ``(2) the food substance is under review under subsection 
        (e)(1)(A) and the Secretary has not yet made a final 
        determination under subsection (e)(2).
    ``(b) Notice to FDA.--
            ``(1) In general.--Any person may, with respect to any 
        intended use of a food substance generally recognized as safe, 
        file with the Secretary a notice proposing inclusion of such 
        food substance on the list described in subsection (c).
            ``(2) Timeframes.--The timeframes for filing of a notice 
        under paragraph (1) are as follows:
                    ``(A) With respect to a food substance used in food 
                offered in interstate commerce as of the date of 
                enactment of the Better Food Disclosure Act of 2025, 
                and, as of such date of enactment, considered to be a 
                food substance generally recognized as safe, not later 
                than 2 years after such date of enactment.
                    ``(B) With respect to a food substance first used 
                in food offered in interstate commerce after the date 
                of enactment of the Better Food Disclosure Act of 2025, 
                not later than 120 days before the first use of the 
                food substance in such food.
    ``(c) Regulations.--Not later than 2 years after the date of 
enactment of the Better Food Disclosure Act of 2025, the Secretary 
shall promulgate regulations to establish the procedures to establish 
and maintain a publicly accessible list of food substances generally 
recognized as safe.
    ``(d) FDA Listing.--
            ``(1) In general.--Not later than 180 days after receiving 
        a notice under subsection (b)(1), the Secretary shall accept 
        such notice and--
                    ``(A) add the food substance to the list described 
                in subsection (c); or
                    ``(B) subject to subsection (e), make a preliminary 
                determination to exclude the food substance from such 
                list.
            ``(2) Effectiveness of notice.--If the Secretary does not 
        make a preliminary determination to exclude a food substance 
        under subparagraph (B) of paragraph (1) by the deadline 
        described in such paragraph, such food substance shall be 
        deemed to be added to the list described in subsection (c).
    ``(e) Excluded or Delisted Substances.--
            ``(1) In general.--If the Secretary makes a preliminary 
        determination under subsection (d)(1)(B) to exclude a food 
        substance for which a notice was submitted under subsection 
        (b)(1) from the list described in subsection (c), or removes a 
        food substance from such list after reevaluation in accordance 
        with section 409B, the Secretary shall require any person using 
        such food substance in food to submit to the Secretary, not 
        later than 180 days after issuance of an preliminary or removal 
        determination, at the option of such person--
                    ``(A) a request for the Secretary to reconsider 
                such preliminary determination or removal 
                determination, including any additional information the 
                Secretary may request in order to make a final 
                determination of whether the food substance is a food 
                substance generally recognized as safe;
                    ``(B) a food additive petition under section 409; 
                or
                    ``(C) a plan for phasing out use of the food 
                substance.
            ``(2) Final determinations.--If a person requests under 
        paragraph (1)(A) that the Secretary reconsider a preliminary 
        determination under subsection (d)(1)(B) to exclude a food 
        substance for which a notice was submitted under subsection 
        (b)(1) from the list described in subsection (c) or the removal 
        of a food substance from such list after reevaluation in 
        accordance with section 409B, not later than 180 days after 
        receiving sufficient information paragraph (1)(A), the 
        Secretary shall make a final determination of whether the food 
        substance is a food substance generally recognized as safe.''.
    (b) Definitions.--Section 201 of the Federal Food, Drug, and 
Cosmetic Act (21 U.S.C. 321) is amended--
            (1) in paragraph (s)--
                    (A) by striking ``, if such substance is not 
                generally recognized, among experts qualified by 
                scientific training and experience to evaluate its 
                safety, as having been adequately shown through 
                scientific procedures (or, in the case of a substance 
                used in food prior to January 1, 1958, through either 
                scientific procedures or experience based on common use 
                in food) to be safe under the conditions of its 
                intended use'';
                    (B) in paragraph (5), by striking ``or'' at the 
                end;
                    (C) in paragraph (6), by striking the period and 
                inserting ``; or''; and
                    (D) by adding at the end the following:
            ``(7) a food substance generally recognized as safe, as 
        defined in paragraph (tt).''; and
            (2) by adding at the end the following:
    ``(tt) The term `food substance generally recognized as safe' means 
any substance the intended use of which results or may reasonably be 
expected to result, directly or indirectly, in its becoming a component 
or otherwise affecting the characteristics of any food (including any 
substance intended for use in producing, manufacturing, packing, 
processing, preparing, treating, packaging, transporting, or holding 
food; and including any source of radiation intended for any such use), 
if such substance is generally recognized, among experts qualified by 
scientific training and experience to evaluate its safety, as having 
been adequately shown through scientific procedures (or, in the case of 
a substance used in food prior to January 1, 1958, through either 
scientific procedures or experience based on common use in food) to be 
safe under the conditions of its intended use, except that such term 
does not include--
            ``(1) food additives, as defined in paragraph (s), that are 
        subject to section 409; or
            ``(2) any article described in subparagraphs (1) through 
        (6) of paragraph (s).''.
    (c) Adulterated Food.--Section 402(a)(2)(C) of the Federal Food, 
Drug, and Cosmetic Act (21 U.S.C. 342(a)(2)(C)) is amended--
            (1) by striking ``or (ii) a new'' and inserting ``(ii) a 
        new''; and
            (2) by inserting ``or (iii) a food substance generally 
        recognized as safe that is not included on the list maintained 
        by the Secretary pursuant to section 409A(c) or is under review 
        pursuant to section 409A(e);'' after ``section 512;''.
    (d) Conforming Amendments.--
            (1) Section 301(ll)(3)(A) of the Federal Food, Drug, and 
        Cosmetic Act (21 U.S.C. 331(ll)(3)(A)) is amended by inserting 
        ``, or the requirements of section 409A, as applicable'' before 
        the semicolon.
            (2) Section 408(l)(5)(B) of the Federal Food, Drug, and 
        Cosmetic Act (21 U.S.C. 346a(l)(5)(B)) is amended by inserting 
        ``listing of a food substance generally recognized as safe 
        under section 409A(c),'' after ``food additive regulation''.
            (3) Section 721(b)(4) of the Federal Food, Drug, and 
        Cosmetic Act (21 U.S.C. 379e(b)(4)) is amended by striking 
        ``while there is in effect a published finding of the Secretary 
        declaring such substance exempt from the term `food additive' 
        because of its being generally recognized by qualified experts 
        as safe for its intended use, as provided in section 201(s)'' 
        and inserting ``if it is included on the list maintained by the 
        Secretary pursuant to section 409A(c)''.
            (4) Section 801(d) of the Federal Food, Drug, and Cosmetic 
        Act (21 U.S.C. 381(d)) is amended by inserting ``food substance 
        generally recognized as safe,'' after ``color additive,'' each 
        place such term appears.
            (5) Section 803(c)(2) of the Federal Food, Drug, and 
        Cosmetic Act (21 U.S.C. 383(c)(2)) is amended by striking ``and 
        color additives'' and inserting ``color additives, and food 
        substances generally recognized as safe''.

SEC. 3. POSTMARKET ASSESSMENT OF FOOD ADDITIVES, COLOR ADDITIVES, AND 
              FOOD SUBSTANCES GENERALLY RECOGNIZED AS SAFE.

    Chapter IV of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 
341 et seq.) is amended by adding after section 409A (as added by 
section 2) the following:

``SEC. 409B. POSTMARKET ASSESSMENT OF FOOD ADDITIVES, COLOR ADDITIVES, 
              AND FOOD SUBSTANCES GENERALLY RECOGNIZED AS SAFE.

    ``(a) In General.--If the Secretary receives a citizen petition or 
a notice from a State governmental official regarding concerns about 
the safety of a food additive for which 1 or more regulations 
prescribing conditions of safe use have been issued under section 409, 
a color additive used in accordance with the requirements of section 
721, or a food substance generally recognized as safe included on the 
list described in section 409A(c), or if the Secretary determines 
through the Secretary's initiative that such a concern exists, the 
Secretary may reevaluate the additive or substance in accordance with 
section 409, 721, or 409A, as applicable, and, as appropriate--
            ``(1) with respect to a food additive, amend or revoke the 
        1 or more regulations issued under section 409 with respect to 
        the food additive;
            ``(2) with respect to a color additive, amend or revoke the 
        1 or more regulations issued under section 409 with respect to 
        the food additive; and
            ``(3) with respect to a food substance generally recognized 
        as safe--
                    ``(A) determine the food substance to be a food 
                additive subject to the requirements of section 409; 
                and
                    ``(B) by rulemaking under section 553 of title 5, 
                United States Code, remove the food substance from the 
                list described in subsection 409A(c).
    ``(b) Priority Considerations.--In considering citizen petitions 
and notices from State governmental officials received under subsection 
(a), the Secretary shall give priority to petitions and notices 
regarding food additives, color additives, and food substances 
generally recognized as safe for which clear and convincing scientific 
evidence supports the concerns raised in the petition or notice.
    ``(c) Safety Information.--The Secretary shall publish in the 
Federal Register a request for safety information for any food 
substance subject to reevaluation under subsection (a).
    ``(d) Review Requirements.--
            ``(1) In general.--Any determination, reevaluation, or 
        final action taken by the Secretary under this section 
        regarding the safety, exclusion, delisting, or reclassification 
        of a food additive, color additive, or food substance generally 
        recognized as safe shall be subject to--
                    ``(A) review and recommendation by individuals 
                serving in positions in the Food and Drug 
                Administration under career appointments and who have 
                relevant scientific and regulatory expertise; and
                    ``(B) the notice and comment rulemaking procedures 
                under section 553 of title 5, United States Code.
            ``(2) Limitation.--The Secretary may not delegate the 
        review under paragraph (1)(A) to--
                    ``(A) an individual occupying a position for which 
                appointment is made by the President; or
                    ``(B) an individual who is not serving in a 
                position in the Food and Drug Administration under a 
                career appointment.''.
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