Bill Text: NY A00512 | 2023-2024 | General Assembly | Amended


Bill Title: Relates to the menstrual product safety and research act and its creation of a research program to determine the risks posed from potential toxins in menstrual products.

Spectrum: Partisan Bill (Democrat 13-0)

Status: (Introduced) 2024-01-03 - referred to health [A00512 Detail]

Download: New_York-2023-A00512-Amended.html



                STATE OF NEW YORK
        ________________________________________________________________________

                                         512--A

                               2023-2024 Regular Sessions

                   IN ASSEMBLY

                                     January 9, 2023
                                       ___________

        Introduced  by M. of A. L. ROSENTHAL, SIMON, GALLAGHER, GLICK, SILLITTI,
          SHIMSKY, REYES, CRUZ, LEVENBERG, TAYLOR, RAGA,  DE LOS SANTOS,  WALKER
          --  read  once  and  referred  to the Committee on Health -- committee
          discharged, bill amended, ordered reprinted as amended and recommitted
          to said committee

        AN ACT to amend the public health law, in relation to the creation of  a
          research program to determine the risks posed from potential toxins in
          menstrual  products;  and  providing for the repeal of such provisions
          upon expiration thereof

          The People of the State of New York, represented in Senate and  Assem-
        bly, do enact as follows:

     1    Section  1.  Short  title. This act shall be known and may be cited as
     2  "the menstrual product safety and research act".
     3    § 2. Title 6 of article 2 of the public health law, as added by  chap-
     4  ter  342  of the laws of 2014, is amended by adding a new section 269 to
     5  read as follows:
     6    § 269. Menstrual product safety and research. 1. For purposes of  this
     7  section,  the  term  "menstrual  products"  means tampons, pads, liners,
     8  cups, sponges, douches, wipes, sprays,  and  similar  products  used  in
     9  conjunction   with   respect  to  menstruation  or  other  genital-tract
    10  secretions.
    11    2. The commissioner shall  provide  for  the  conduct  or  support  of
    12  research by the department to determine the extent to which the presence
    13  of  dioxins, synthetic fibers, chlorine, and other components (including
    14  contaminants and substances used as  fragrances,  colorants,  dyes,  and
    15  preservatives) in menstrual products:
    16    (a) poses any risks to the health of individuals who use the products,
    17  including risks relating to cervical cancer, endometriosis, infertility,
    18  ovarian  cancer,  breast  cancer,  immune  system  deficiencies,  pelvic
    19  inflammatory disease, toxic shock  syndrome,  and  bacterial  and  yeast
    20  infections; and

         EXPLANATION--Matter in italics (underscored) is new; matter in brackets
                              [ ] is old law to be omitted.
                                                                   LBD00712-02-3

        A. 512--A                           2

     1    (b) poses any risks to the health of biological children born to indi-
     2  viduals  who  used  such  products  during  or  before  the  pregnancies
     3  involved, including risks relating to fetal and childhood development.
     4    3.  Research  under  subdivision  two  of  this  section shall include
     5  research to confirm the data on  menstrual  products  submitted  to  the
     6  United  States  food  and  drug  administration by manufacturers of such
     7  products.
     8    4. Such research projects shall be completed within four years of  the
     9  effective date of this section.
    10    5.  Within  one  year  of the completion of such research, any conclu-
    11  sions, recommendations and proposals for implementing  such  recommenda-
    12  tions  shall  be transmitted to the governor, the temporary president of
    13  the senate, the speaker of the assembly, the chair of the senate  health
    14  committee,  and  the  chair  of the assembly health committee, and shall
    15  also be made available to the public.
    16    § 3. This act shall take effect on the ninetieth day  after  it  shall
    17  have  become  a  law  and shall expire and be deemed repealed five years
    18  after such date.
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