Are you trying to avoid an unnecessary or non-consumer-friendly ingredient declaration? Are you looking to build a clean label? Or do you ever wonder if a specific ingredient falls under the definition for “incidental additives” and may be exempt from an ingredient listing?
Earlier this year, Q1 held their 6th Annual Food Labeling Conference in Arlington, Virginia, where over one hundred representatives of the food industry gathered to discuss evolving regulatory issues within the food world. In today’s fast track to launch environment and short product lifecycles, organizations are challenged by the slow movement of supporting regulations and are forced to make calculated risks to satisfy their ever-demanding consumers. There were many excellent discussions and presenters at this conference, but they all had a basic theme that can be summarized in five key takeaways: Continue Reading
Did you ever wonder why your favorite ice cream has the nutrition information for a ⅔ cup? It’s because the Food and Drug Administration (FDA) has developed serving sizes for multiple categories referred to as Reference Amounts Customarily Consumed (RACC).
The ice cream you purchase from any retailer will be using the same serving size (household measure may differ), so you’re able to easily compare the nutrition information. The FDA took a look at the RACC’s and updated them with the 2016 Nutrition Facts Label to better fit what people are actually consuming in one sitting.
The evolving regulatory and consumer demands for “healthy” products with “clean labels” are challenging food and beverage manufacturers in North America. How can sugar, sodium and fat levels be reduced in products in order to meet public health goals, yet the products still retain a “crave-able” flavor and texture to satisfy consumer expectations?
In the United States, two different regulatory organizations oversee food labeling for different product types. The first post in our blog series broke down which food products fall under the labeling jurisdiction for the United States Department of Agriculture (USDA) and the Food and Drug Administration (FDA), as well as how the above affects a product’s statement of identity. Now that we’ve established that base, we will delve deeper into the various differences between USDA and FDA food labeling, from the way nutrition claims are handled to safe handling instructions and everything in between. Below are six essential differences between food labeling guidelines for the two regulatory bodies:
The claims and information on a product’s label allow customers to make informed purchasing decisions. However, consumers may not realize when choosing between a frozen veggie or sausage pizza that the information on the labels for these two similar products is actually regulated by two different government agencies.
The United States Department of Agriculture (USDA) and the Food and Drug Administration (FDA) oversee labeling for food items sold in the United States. The labels on products regulated by these two entities do share many common features, such as a statement of identity, net quantity declaration, nutrition label, ingredient statement and responsible party information. However, there are some differences in the information found on their respective labels. As part one of our two-part series on the differences between USDA and FDA labeling requirements, let’s examine the overlapping product categories and how the statement of identity can vary based on which entity oversees your product type. Continue Reading
The old saying is to never judge a book by its cover, but consumers regularly judge a food item by its label. Increasingly, customers are spending more time reading every part of a product’s label before they buy it, from the claims on the front to the nutrition information to the ingredients list. Here at Mérieux NutriSciences, our Labeling Compliance & Nutrition Services team works to help food manufacturers create compliant food, menu and nutrition labels with federal regulations, including Food and Drug Administration (FDA), United States Department of Agriculture (USDA) and Health Canada. Continue Reading
When you go to the store and pick up a container of strawberry yogurt, you probably don’t put much thought into how it gets its strawberry flavor. Does it contain actual strawberries or does it only contain an artificial flavor? Both natural and artificial flavors are frequently used to impart or enhance specific flavors in food products.
Before we delve into how natural and artificial flavors affect labeling, let’s look at the difference between the two. The FDA considers a natural flavor to be an additive to a product, “which contains the flavoring constituents derived from a spice, fruit or fruit juice, vegetable or vegetable juice, edible yeast, herb, bark, bud, root, leaf or similar plant material, meat, seafood, poultry, eggs, dairy products, or fermentation products thereof, whose significant function in food is flavoring rather than nutritional.” So, natural flavors generally come from plant or animal sources, such as the natural strawberry flavor for a yogurt. Conversely, any substance used to flavor a product that is not derived from one of the sources listed in the natural flavors definition is considered an artificial flavor by the FDA. Continue Reading