SENATE, No. 2266
STATE OF NEW JERSEY
222nd LEGISLATURE
PRE-FILED FOR INTRODUCTION IN THE 2026 SESSION
Sponsored by:
Senator M. TERESA RUIZ
District 29 (Essex and Hudson)
Senator LINDA R. GREENSTEIN
District 14 (Mercer and Middlesex)
Co-Sponsored by:
Senators Cryan, Diegnan, Singleton and Singer
SYNOPSIS
Limits perfluoroalkyl and polyfluoroalkyl substances in menstrual products.
CURRENT VERSION OF TEXT
As reported by the Senate Commerce Committee on October 5, 2026, with amendments.
An Act limiting perfluoroalkyl and polyfluoroalkyl substances in menstrual products and supplementing P.L.1960, c.39 (C.56:8-1 et seq.).
Be It Enacted by the Senate and General Assembly of the State of New Jersey:
1. a. As used in this act:
1“Intentionally added PFAS” means PFAS added to a product or a product’s components to provide a specific characteristic, appearance, or quality or to perform a specific function. The term includes any degradation byproducts of PFAS but excludes a technically unavoidable trace quantity of PFAS as measured in total organic fluorine.1
“Menstrual product” means a product manufactured for the purpose of catching menstruation and vaginal discharge, including but not limited to a tampon, sanitary pad, disc, menstrual cup, and underwear. The term shall include both disposable and reusable products.
“Perfluoroalkyl and polyfluoroalkyl substances” or “PFAS” means the same as defined in subsection k. of section 1 of P.L.2023, c.243 (C.56:8-229).
1[“Regulated perfluoroalkyl and polyfluoroalkyl substances” or “Regulated PFAS” means:
(2) The presence of PFAS in a product or product component above a technically unavoidable trace quantity, as measured in total organic fluorine.]1
b. A manufacturer of menstrual products shall not sell, distribute, or offer for sale or use in this State any menstrual product containing 1[regulated] intentionally added1 PFAS.
c. (1) The Department of Environmental Protection shall establish a system for manufacturers to periodically test for the presence of 1[regulated] intentionally added1 PFAS in menstrual products, to be conducted by a laboratory approved by the commissioner.
(2) The commissioner shall publish on the department’s Internet website a list of approved laboratories and a list of acceptable testing methods to be used to satisfy the requirements of paragraph (1) of this subsection.
d. The results of a test conducted pursuant to subsection c. of this section shall be available to the Department of Health for inspection upon request to the manufacturer or laboratory.
e. A violation of the provisions of this section shall constitute an unlawful practice for the purposes of P.L.1960, c.39 (C.56:8-1 et seq.), and the violator shall be subject to all the remedies and penalties available pursuant to P.L.1960, c.39 (C.56:8-1 et seq.).
2. This act shall take effect on the first day of the 25th month next following enactment, except that the Commissioner of Environmental Protection and the Commissioner of Health may take any anticipatory administrative action in advance as may be necessary for the implementation of this act.