المكملات الغذائية المصرح بها من هيئة الغذاء والدواء الأمريكية FDA

في أمريكا ليس ضروري الحصول على موافقة من ال FDA قبل طرح المكمل الغذائي بالأسواق . ال FDA دورها فقط الرقابة على أمان المنتج و مطابقته لل label بعد نزوله الأسواق

بمعنى أنه لا يوجد شئ أسمه مكمل مصرح من ال FDA . و لكن ربما تقوم ال FDA لاحقا بحظر بعض المكملات أو المكونات ..

• Federal law requires that every dietary supplement be labeled as such, either with the term "dietary supplement" or with a term that substitutes a description of the product's dietary ingredient(s) for the word "dietary" (e.g., "herbal supplement" or "calcium supplement").
• Federal law does not require dietary supplements to be proven safe to FDA's satisfaction before they are marketed.
• For most claims made in the labeling of dietary supplements, the law does not require the manufacturer or seller to prove to FDA's satisfaction that the claim is accurate or truthful before it appears on the product.
• In general, FDA's role with a dietary supplement product begins after the product enters the marketplace. That is usually the agency's first opportunity to take action against a product that presents a significant or unreasonable risk of illness or injury, or that is otherwise adulterated or misbranded.
  
  https://www.fda.gov/ForConsumers/ConsumerUpdates/ucm050803.htm
  
  
  

 

في تغييرات طفيفة كل فترة .