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The FDA wants to remove petroleum-based synthetic dyes from food and beverages by the end of 2026, replacing them with natural alternatives. This directive, which is a voluntary program and not a ban, mirrors recent state-level legislative actions that center around a small percentage of the population who may be impacted by some synthetic dyes in high quantities. While on the surface, the move to replace artificial food dyes with natural dyes may seem straightforward, there are numerous reformulation challenges.
With the FDA’s requested transition date by the end of 2026, the countdown has now started with only 19 months for products to be identified, assessed, reformulated, and commercialized. Reformulating each product will have its own unique challenges. For example, the general rule is the more vibrant and brighter the color, the more difficult it will be to substitute.
Here are six key considerations when planning a reformulation:
From consumer expectation to product properties and price, the road to reformulation is going to be a bumpy one as companies adapt to meet the FDA’s aggressive timeline. An important stop on the road to reformulation will be IFT FIRST this summer where the food science community will gather to address the future of food additives and artificial food dyes, among other important topics. The three-day event will identify data-driven approaches to accelerate food formulation development as well as provide an in-depth examination of food additives reformulation and regulatory challenges, courtesy of a panel of top food industry leaders. Product developers seeking reformulation help beyond educational sessions will find a variety of solutions on the expo floor, which will include the unveiling of revolutionary new product development tool that will ease the burden of the 19-month deadline from the FDA.