U.S. FDA Labeling Requirements

The U.S. Food and Drug Administration (FDA) defines “labeling” as “all labels and other written, printed, or graphic matters (1) upon any article or any of its containers or wrappers, or (2) accompanying such an article.” This may include packaging, instructions, product inserts, websites, and other promotional materials.

Labeling mistakes result in more than 22% of all detentions in the United States. Metti FDA can review your label for compliance with FDA regulations. In addition to a report of recommended changes, you will receive a print-ready graphic file of your revised label.

U.S. Food and Drug Administration

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