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NotEach product sold On the shelves is sure for everyone. This is why the warning labels are extremely important, because they inform us the risks that could be associatedwith some articles- And if these risks apply to us. Unfortunately, labels can also be misleading: the United States Food and Drug Administration (FDA) alerts buyers that the supplements or the food they buy could be dangerous if the packaging includes two specific words. Read the rest to find out what you should be careful when you shop.

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In the interest of public health and security, the FDA is responsible for regulating a number of products that consumers use, including food and food supplements. But unlike most of the drugs you see on the market, the agency does not have to approve food and supplements before being sold to the general public. According to the FDA, it is nothave pre-market approval (PMA) for one or the other, except in some cases.

The PMA "is the FDA process of scientific and regulatory examination to assess the safety and efficiency" of certain products before they are marketed and sold to consumers, explains the agency. ThisFour -step approval examination process is the "most rigorous" type of the marketing application required by the FDA.

In an update of consumers of May 10, the FDABuyers alert to look outside For these two words on supplements and food products: "FDA approved". According to the agency, some companies try to use this sentence on their website, their advertisements or their packaging for a product, even when the product did not receive the approval of the FDA before being put on the market .AE0FCC31AE342FD3A1346EBB1F342FCB

"The FDA is responsible for protecting public health by regulating human drugs and organic products, animal medicines, medical devices, tobacco products, food (including animal food), cosmetics and electronic products Who emit radiation, "said the agency. "But all these products do not undergo approval before the market, that is to say that an examination of the safety, quality and efficiency of FDA experts and agency approval Before a product can be sold to consumers. In some cases, FDA application efforts are focused on products after they are already for sale. "

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Regarding food, many products do not have to obtain approval from the FDA before being sold to buyers. The agency does not approve of food products, individual food labels, medical foods or even infant preparations. "All declarations on food products must be truthful and non -misleading - and must comply with any regulatory requirement for the type of declaration, as the case may be," warned the FDA.

But there are some exceptions for additives in food. The FDA said that it had the power to approve certain ingredients before being used in food, which includes food additives and color additives. Companies seeking to add new food additives or color additives to food are responsible for providing the FDA information that shows that additives are safe, and the agency will assess this safety data for approval.

"Certain food ingredients, such as those considered" generally recognized as safe "(fat) for their conditions of use by scientific experts, do not require the prior approval of the market by the FDA", explained the agency. "The FDA has a process of voluntary notification under which a manufacturer can submit a conclusion that the use of an ingredient is fatty."

According to the FDA, companies manufacturing food supplements are responsible for ensuring that their own products are safe before marketing and selling them, but they do not have to apply for the agency beforehand. "The FDA is not authorized to approve food supplements for safety and efficiency. In fact, many food supplements can be marketed without even informing the FDA," warned the agency.

The only exception to this is that companies trying to sell supplements containing new food ingredients (NDIS) must submit a security notification prior to the FDA at least 75 days before marketing their product. Even in this case, however, the supplement cannot be considered "approved by the FDA". It is only once an additional supplement is sold that the agency can act against it if public health problems occur regarding product safety or an ingredient.

"The FDA logo is reserved for the official government.

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