Is the FDA Trying to Take Away Your Vitamins?

Written By

Published December 20, 2011

What began as a murmur last year about a possible ban on thousands of dietary supplements in the U.S. has reached cacophonous levels over the last few months, as the Food and Drug Administration indicated its intent to regulate “new dietary ingredients” in current and future products.

What does this mean? And, more importantly, how might it affect you and your health?

This past summer, the FDA issued a draft of guidelines for complying with the New Dietary Ingredient (NDI) notification protocols. Translation: Any company or individual wishing to sell or develop a supplement containing new ingredients would have to notify the FDA of their intent. A “new” ingredient is defined as one added after 1994, when Congress passed the Dietary Supplement Health and Education Act (DSHEA). If the FDA deems a new ingredient unsafe or unscientific, the entire supplement can be removed from the market.

Just. Like. That.

Think about how many different conditions, serious or not, people treat or keep in check with vitamins, minerals, herbs or other alternative therapies. Arthritis? Yup. Headaches? Check. Menstrual cramps? Absolutely. Cancer? You bet. For almost every ache, pain or illness, there is a coordinating supplement that may not necessarily cure, but offers the possibility of relief, often in a much more natural form than Western medicine.

Read entire article HERE.

Leave a Reply

Your email address will not be published. Required fields are marked *