What’s Next for FDA Imports? Preparing for Policy Shifts in 2025

Episode Summary: In this episode of FDA Imports – Cross-Border Compliance, host Kevin continues the conversation with attorney Benjamin L. England on the complexities of food labeling compliance. They dive into the common mistakes companies make, misbranding risks, and the legal consequences of misleading claims. The discussion covers nutrient content claims, health claims, organic and natural labeling, and how businesses can avoid costly litigation and regulatory issues. Whether you're a food manufacturer, importer, or distributor, this episode provides crucial insights into ensuring label accuracy and compliance with FDA regulations. Timestamps: 00:00 – Introduction to the episode and guest Benjamin L. England 00:06 – Recap of the previous episode on food labeling basics 00:27 – Common mistakes in food labeling 01:09 – Technical misbranding risks: Front and side panel requirements 02:24 – Artificial flavoring, food colorings, and compliance issues 04:35 – Understanding nutrient content claims (e.g., "good source of vitamin D") 07:02 – The legal risks of false or misleading claims in food labeling 09:34 – Health claims: FDA regulation and enforcement 12:00 – What does "natural" mean? FDA policies vs. legal risks 13:58 – Organic labeling and USDA vs. FDA jurisdiction 14:09 – FDA’s enforcement at the border and compliance strategies 15:25 – How Benjamin L. England & Associates helps companies navigate compliance 16:03 – Avoiding violations and managing disputes with FDA About the Show: FDA Imports – Cross-Border Compliance is a podcast dedicated to helping businesses navigate U.S. regulatory compliance for imported foods, drugs, medical devices, and cosmetics. Hosted by industry experts, each episode provides practical insights on FDA, USDA, and CBP regulations, helping manufacturers, importers, and exporters stay compliant and competitive in the U.S. market.