Artificial flavors is an umbrella term covering over 2,000 synthetic chemical compounds used to mimic natural flavors. Under FDA regulations, manufacturers are not required to disclose which specific chemicals are used, only that 'artificial flavors' are present.
AAP raised concern about the lack of pediatric safety data for the thousands of chemicals that fall under 'artificial flavors.' The term provides zero transparency: a parent cannot determine which chemicals their child is consuming. Higher concern in beverages due to larger volumes consumed.
All children consuming products with artificial flavors. Risk assessment is impossible because specific chemical identity is not disclosed.
| Country | Status |
|---|---|
| United States | Permitted. FDA allows 'artificial flavors' as an ingredient label without disclosing specific compounds. Many flavor chemicals enter the market through the GRAS self-determination process without FDA review. |
| European Union | Permitted with more specific labeling requirements. Individual flavoring substances are evaluated by EFSA. |
| Canada | Permitted. |
| Australia | Permitted. |