WASHINGTON — If you’ve ever seen the astonishing array of infant formula sold in supermarkets, you might wonder if the stuff can really make your baby smarter, allergy-proof, or less colicky, as advertised.
The Food and Drug Administration wonders the same thing.
On Thursday, the FDA suggested that the $3 billion infant formula industry consider proving its claims before selling the products.
On supporting science journalism
If you're enjoying this article, consider supporting our award-winning journalism by subscribing. By purchasing a subscription you are helping to ensure the future of impactful stories about the discoveries and ideas shaping our world today.
In an unusual move, the agency served up a set of scientific standards for infant formula manufacturers to meet, before touting their products for treatment or prevention of certain medical conditions.
This draft proposal suggests that manufacturers conduct research trials and otherwise gather evidence to back assertions of how their products actually function in a baby’s body. Manufacturers and others have 60 days to comment, before the agency adopts a final guideline.
The move marks the first time that the FDA has proposed a standard, even a voluntary one such as this, for companies making health claims about a specific food. (The FDA did develop a standard for dietary supplements broadly.) In recent years, formula manufacturers have increasingly developed specialized products, often with vitamins, other nutrients, or additives, which they target to parents eager for their babies to have superior immune systems, digestion, or brains.
“Because infancy is a unique, vulnerable period when critical growth and development occur,” the FDA wrote, “great care is necessary to ensure the safety of all modifications to infant formula, even if the purpose of the modification is to more closely mirror the composition and health benefits of human milk.”
Agency spokeswoman Lauren Kotwicki said the FDA has seen an increase in the use of health claims on infant formula labeling and that manufacturers who want to use such claims have asked the agency how to substantiate them.
The FDA’s action follows publication of a report in the May 2016 issue of Clinical Pediatrics, which studied the labels of 22 infant formula products and found that 13 made claims about treating colic and gastrointestinal symptoms without proof.
“There is insufficient evidence to support the claims that removing or reducing lactose, using hydrolyzed or soy protein or adding pre-/probiotics to formula benefits infants with fussiness, gas, or colic,” the authors wrote. “Yet claims like ‘soy for fussiness and gas’ encourage parents who perceive their infants to be fussy to purchase modified formula. Increased regulation of infant formula claims is warranted.”
Dr. Peter Belamarich, a professor at Albert Einstein College of Medicine and the study’s lead author, welcomed the FDA’s action.
“They are trying to reign it in a little bit,” Belamarich said. “It’s an attempt to put the claims under greater scientific scrutiny. It’s a good and terrifically important development.”
Belamarich, who works at the Children’s Hospital at Montefiore, said he sees plenty of confused parents.
“We see it every day, Belamarich said. “People switching formulas in the hope that what is most often normal baby behaviors is going to be treated by switching formula. There are so many products and so many claims.”
Republished with permission from STAT. This article originally appeared on September 7, 2016
