Because the FDA generally classifies the products it regulates based on intended use and ingredients found therein, among other considerations, an initial stage in determining how a product will be regulated is by looking to the intended use. The FDA generally determines the intended use of a product based on statements, called “claims,” made about a product, i.e., what the marketer claims the product can do. In addition to intended use-type claims, certain claims are made about the ingredients found in a product, such as organic and natural claims.
By understanding the types of claims under FDA regulations and federal law, a FDA regulatory lawyer can help you avoid making improper claims that may cause your products to be subject to heightened regulation.
FDA Regulations and Organic and Natural Claims
While there are different types of claims, i.e., health claims, disease claims, structure-function claims, some claims may cause a product to be subject to heightened regulation. For example, if a product is otherwise classified as a food but its labeling contains disease claims, the FDA will classify this product as a drug. On the other hand, certain claims, called structure-function claims, may be made about dietary supplement products and, if done correctly, will not cause these products to be subject to heightened regulation. Thus, when marketing a FDA-regulated product, it is critical to understand what types of claims may be used for your particular product and to ensure that these claims are properly worded.
Organic and Natural Claims – Labeling Reviews
At Mejia Shehadeh Giannamore, PLLC, a FDA regulatory lawyer can help you ensure FDA compliance by:
- Reviewing your product labeling, including your actual product labels, websites, and other marketing materials, to determine whether your claims are in compliance with the laws and regulations enforced by the FDA and other responsible government agencies;
- Providing guidance with respect to any changes that must be made to your organic and natural claims in order for you to achieve and maintain FDA compliance;
- Suggesting alternative language that reduces the risk of FDA enforcement action, should you have problematic claims in your product labeling that may result in FDA action.