2022 Act: More Power to FDA to Control Dietary Supplements

an act has passed in the US Senate that gives the FDA more control over supplement companies.
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Specifically, in regard to dietary supplements, the Act would require that companies actually list their products with the FDA. The information required to be submitted in connection with the listing includes:
The name of the supplement
The name and address of the manufacturer, packer, or distributor appearing on the label
It will hopefully expose companies like Austin Nootropics, and many others, who claim to actually manufacture their own NMN in the USA, when most people know this is highly unlikely, they buy from China like all other companies, then package it in the USA and claim Made in the USA)
Contact information for the owner or operator (again this is good, I hope this as a minimum includes business address, email and phone number.
Many supplement companies limit their “contact us” to an email address, a web based instant messaging application, or even just a Facebook page).
This is usually because they are operating a drop-shipping business working out of out of their home or garage, or keep very little stock on hand, And some companies give double-speak type reasons for being allusive and difficult to track down
The FDA will also require The business name and mailing address of all locations in which the dietary supplement is manufactured, packaged, labeled, or held, Again let’s hope by manufacturer they mean the Chinese company that actually produces the Raw product, and not the US based reselling company
A list of all ingredients in each supplement
Let’s hope supplement companies don’t try to hide behind the “proprietary blend” loophole)
The FDA will also want to know
The number of servings per container; directions for use; warnings, notice, and safe handling statements; allergen statements; any health or structure/function claims; and the dietary supplement product listing number.
I agree with this, very close to what most reputable companies now do anyway.
Subject to limited exceptions, this information would be made publicly available in a searchable electronic database.
This would be a great resource, and one that I think many of the fly-by-nigh companies would not like to see come to fruition
This looks like it is only applicable to USA based companies. I would hope that those wishing to sell from abroad would have to adhere to the similar standards.
Also, there is no mention of initial testing, or random testing, so as long as a company sets up and fulfills all the criteria, they can still sell fake products, it still looks like the FDA will still reply on concerned citizens reporting nefarious company actives
The Act also proposes changes to the regulation of cosmetics.
Although not wholly applicable, there are some supplements such as NAD creams and serums that I think may fall into this category.
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