The U.S. Food and Drug Administration has proposed a new definition for what constitutes "healthy" food, taking a more holistic look at nutrition and food groups instead of focusing solely on a few vitamins, minerals and nutrients.
The proposal has provoked a mixed response from nutritionists, the food industry and public health officials, highlighting the thorny task of broadly regulating something as personal as an individual diet.
Nutrition science has evolved significantly since the FDA last defined "healthy" in 1994 — and so has the prevalence of obesity and diet-related diseases.
And because food packaging can be highly influential on both consumers and food manufacturers, the FDA believes a "healthy" label will lead to better products and eating habits.
"It makes sense that they decided to update the definition and make it consistent with the science," said Marlene Schwartz, director of the Rudd Center for Food Policy and Health at the University of Connecticut. "But when you just focus on healthy and are silent on the less healthy, you're not having the impact you could if you actually communicated the whole spectrum."
The FDA's ultimate goal is to reduce the prevalence of diseases that can stem from poor diets, such as cardiovascular disease, type 2 diabetes and certain cancers, as well as obesity.
Most Americans eat far more sodium than is recommended — largely from processed food — while 80% of Americans do not eat enough fruit and 90% do not eat enough vegetables, the agency said.
And so, if the FDA's goal is to make Americans healthier, some nutritionists say the updated definition misses the mark.