Sen. Richard Durbin (D-IL) sent a letter on Oct. 16 to the U.S. Food and Drug Administration (FDA) urging the agency to publish a list of electronic nicotine delivery system (ENDS) products for which it has received a premarket tobacco product application (PMTA). Manufacturers of ENDS products were required to submit a PMTA to FDA by Sept. 9, 2020, to remain on the market. Without a publicly available list, retailers – including travel centers – will not know which products are legal for them to sell. More