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	<title>Translations:Dietary supplement/42/en - Revision history</title>
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	<updated>2026-11-14T21:49:59Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<title>FuzzyBot: Importing a new version from external source</title>
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		<updated>2023-10-19T22:41:25Z</updated>

		<summary type="html">&lt;p&gt;Importing a new version from external source&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;In the United States and Canada, dietary supplements are considered a subset of foods, and are regulated accordingly. The U.S. Food and Drug Administration (FDA) monitors supplement products for accuracy in advertising and labeling. Dietary supplements are regulated by the FDA as [[food product]]s subject to compliance with current [[Good Manufacturing Practice]]s (CGMP) and labeling with science-based ingredient descriptions and advertising. When finding CGMP or advertising violations, [[FDA warning letter]]s are used to notify manufacturers of impending enforcement action, including [[search and seizure]], [[injunction]], and [[fine (penalty)|financial penalties]]. Examples between 2016 and 2018 of CGMP and advertising violations by dietary supplement manufacturers included several with illegal compositions or advertising of vitamins and minerals.&lt;/div&gt;</summary>
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