Titanium Dioxide And Zinc Oxide Sunscreen-Does The Fda Require Titanium Dioxide To Be Labeled

The U.S. Food and Drug Administration (FDA) has specific labeling requirements for food, drugs, and cosmetics, which include the use of titanium dioxide.

For food and dietary supplements, titanium dioxide is often used as a color additive. The FDA requires that all color additives, including titanium dioxide, be declared on the product label. If a food or dietary supplement contains titanium dioxide, it must be listed in the ingredient statement on the product’s label.

In the case of drugs, if titanium dioxide is used as an ingredient in a drug product, it must also be included in the labeling, typically in the list of inactive ingredients.

For cosmetics, the FDA does not have the same premarket approval process for color additives as it does for food and drugs. However, once a color additive like titanium dioxide is listed as safe for use in cosmetics (it is generally recognized as safe when used appropriately), it must be listed on the product label. This includes the name of the color additive, and in some cases, the specific color it imparts.

It’s important to note that the labeling requirements can vary depending on the context in which titanium dioxide is used and the regulations in place at the time of product manufacture. Consumers can refer to the specific product label or to the FDA’s guidelines for more detailed information.