FDA moves to revoke 2 food dye authorizations

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1–2 minutes

Summary

FDA revoked Orange B’s food-use authorization and proposed doing the same for Citrus Red No. 2.

Why this matters

The actions would further narrow the use of older petroleum-based food dyes in the U.S. food supply. For companies and the public, the proposal also opens a formal comment period through Aug. 24, 2026.

The U.S. Food and Drug Administration said July 22, 2026, that it took two steps involving petroleum-based color additives used in food.

The agency issued a final order revoking the authorized use of Orange B and proposed revoking the authorized use of Citrus Red No. 2.

According to the FDA, it proposed revoking Citrus Red No. 2 because the agency tentatively concluded that industry had abandoned its use. Citrus Red No. 2 has been authorized since 1959 for coloring the skins of mature oranges.

The FDA said it also issued a final order revoking Orange B after reviewing public comments and finding no new information that changed its conclusion that industry had abandoned that use.

“The Trump Administration is taking decisive action to strengthen the safety of America’s food supply,” said Health and Human Services Secretary Robert F. Kennedy Jr. “By working to eliminate outdated authorizations for petroleum-based color additives that are no longer used, we are modernizing our food safety regulations and helping to Make America Healthy Again.”

“The FDA is committed to maintaining a science-based, modern regulatory framework that reflects current manufacturing practices and marketplace realities,” said Acting FDA Commissioner Kyle Diamantas. “By working to remove outdated and unnecessary authorizations under President Trump’s regulatory reform agenda, we are ensuring our regulations remain effective, transparent, and aligned with the agency’s public health mission.”

The FDA will accept public comments on the proposed revocation of Citrus Red No. 2 for 30 days, through Aug. 24, 2026. Comments may be submitted through the Federal eRulemaking Portal under docket FDA-2026-N-6304 or mailed to the agency’s Dockets Management Staff in Rockville, Maryland.

After reviewing comments, the agency said it will decide whether to finalize the proposed revocation.

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