Category: FDA

  • Proposed Amendment Would Provide Funds for FDA Oversight of CBD

    Rep. Jerry McNerney (D-Calif.), in partnership with the Natural Products Association, has reportedly filed an amendment to the House Agriculture appropriations bill that would give the U.S. Food and Drug Administration (FDA) funding to undertake the process to identify a safe daily intake level of cannabidiol (CBD). “Since the passage of the 2018 Farm Act…

  • FDA Issues Statement on PFAS in Food

    The U.S. Food and Drug Administration (FDA) has issued a statement on per- and polyfluoroalkyl substances (PFAS) in food following a presentation published in the media that indicated the agency found the substances in meat, fish and chocolate. “Overall, our findings did not detect PFAS in the vast majority of the foods tested,” the statement…

  • Guidance Finalized for Added Sugar Labeling in Syrups

    The U.S. Food and Drug Administration has finalized guidance on labeling for added sugars in single-ingredient packages of “pure honey, pure maple syrup, and other pure sugars and syrups, which are not required to bear the words ‘Includes Xg Added Sugars’ but must still include the percent Daily Value (DV) for added sugars on their…

  • FDA Proposes Third-Party Food Safety Certification

    The U.S. Food and Drug Administration (FDA) has indicated that it will seek public comment on a proposal that would allow the accreditation of third-party certification bodies “to conduct food safety audits of eligible foreign food facilities, and issue food and facility certifications, pursuant to the FDA Food Safety Modernization Act.” The notice responds to…

  • Dietary Guidelines Meetings Announced

    The U.S. Department of Agriculture and Health and Human Services have announced meetings to hear public comments on the 2020 dietary guidelines revisions. The 2020 Dietary Guidelines Advisory Committee will allow three-minute pre-registered comments from the public at its meetings on July 11, 2019, and January 25, 2020, and registration for the July meeting closes…

  • FDA Recommends Standardized Use of “Best If Used By”

    The U.S. Food and Drug Administration (FDA) has sent a letter to food and beverage manufacturers recommending that they primarily use “Best If Used By” on their packages to help consumers who may be confused by the use of the phrase “Sell By.” The letter explains that the Grocery Manufacturers Association and Food Marketing Institute…

  • FDA Issues Guidance on “Potassium Chloride Salt”

    The U.S. Food and Drug Administration (FDA) has issued draft guidance for industry on the use of “potassium chloride salt” on food labels as an acceptable alternative to the use of the common or usual name “potassium chloride.” The guidance indicates that the agency recognizes that food manufacturers “wishing to reduce sodium chloride in their…

  • FDA Draft Guidance Excludes Allulose from Added Sugar Disclosure

    The U.S. Food and Drug Administration (FDA) has issued draft guidance allowing food manufacturers to exclude allulose when calculating the amount of added sugars a product contains. Allulose is “approximately 70 percent as sweet as sucrose,” according to a comment FDA received, and “does not have the metabolic properties of fructose or other sugars and…