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FDA Response Confirms Senators On Right Trail About N.Y. Herbal Product Tests

 
• By Malcolm Spicer

“FDA does not use DNA sequencing by itself to analyze an herbal extract for phytochemicals,” Associate Commissioner for Legislation Thomas Kraus tells Senators Hatch and Heinrich. The senators gave FDA an opportunity, without asking for a comment on an ongoing New York investigation, to describe the agency’s regulation of supplement manufacturing.

FDA’s explanation to supplement industry allies in the Senate that using DNA barcoding alone is not appropriate for botanical ingredient identity testing could quiet New York officials’ allegations that herbal products sold in the state are adulterated.

The agency responded March 18 to a request from Sens. Orrin Hatch, R-Utah, and Martin Heinrich, D-N.M

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