The U.S. FDA is currently reviewing petitions for gardenia blue, safflower extract, and carrot oil as approved natural food colours. These are petitions under review — not final approvals. Here is what the filings cover and what food companies should do next.
In April 2025, the FDA announced it would support an industry-led transition away from petroleum-based synthetic food dyes and would accelerate its review of naturally derived colour additives. These three petitions are a direct result of that shift — filed by industry groups who want to expand the approved palette of natural food colours available in the United States.
The move reflects a broader pattern in food manufacturing. Consumers and regulators in multiple markets are pushing for cleaner labels, and food companies are responding. For food manufacturers sourcing food colours, the FDA's direction has practical implications for product development, ingredient sourcing, and labelling.
Each petition addresses a different colour, a different set of food categories, and a different regulatory situation. Together they reflect the range of activity happening as the food industry moves toward natural colourants.
Gardenia (genipin) blue was approved by the FDA in 2025 for use in selected drinks and confectionery. The new petition asks the FDA to permit its use at levels consistent with good manufacturing practice in a wider range of products — including confectionery, desserts, beverages, dairy products, snack foods, and chewable tablets.
The filing also proposes tightening the arsenic specification from 2 parts per million to 1 part per million. Ingredient specifications like this define the purity and quality requirements a colour additive must meet — a stricter limit is generally a positive sign for ingredient quality.
Safflower extract was provisionally listed as an exempt colour additive in 1962 — but that listing was removed just two years later in 1964. This petition is not an expansion of an existing authorisation. It is asking the FDA to reconsider safflower extract for modern food applications from the beginning.
The proposed uses include beverages, chewing gum, breakfast cereals, desserts, dairy products, candy, salad dressings, and soup broths. If approved, safflower extract could offer manufacturers a plant-based option for yellow, orange, or warm-toned product applications.
Carrot oil is already exempt from certification and may be used to colour foods generally at levels consistent with good manufacturing practice. This petition does not seek a new approval — it asks the FDA to update the existing rules to permit acetone as a solvent during carrot oil production.
The filing also proposes adding heavy-metal limits and including additional accepted names for carrot oil in the regulations. Clear specifications help suppliers and food manufacturers align production methods with regulatory requirements and support more consistent quality across the supply chain.
Moving from a synthetic food dye to a natural colour is not a simple one-for-one swap. Natural food colours can behave very differently from synthetic dyes across a range of performance factors that matter to food manufacturers.
A successful reformulation requires more than replacing one ingredient with another. Product development teams need to evaluate natural food dyes for performance, sourcing, cost, and labelling implications before committing to a switch — regardless of what the FDA eventually approves.
The FDA has not finalised any of these three petitions. Until a final rule is issued, the proposed uses are not authorised. Here is a practical approach for food manufacturers and product development teams:
The FDA is reviewing petitions for gardenia blue, safflower extract, and carrot oil — and that review reflects a clear directional shift in how the agency is approaching food colour regulation. But none of these are approved yet, and food companies should not treat the proposed uses as authorised until a final rule is in place.
What food manufacturers can do now is prepare: evaluate natural colour performance in your formulations, understand your sourcing options, and build the internal knowledge you will need to move efficiently once the FDA acts.
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