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The Rosenstock et al

FDA guidance for RUO-labeled in vitro diagnostic products explains that RUO labeling is meant to identify materials in a laboratory research phase and distinguish them from diagnostic contexts [16]

This is directly relevant to the specific "50-100x bioavailability, 2-3x better results" figures mentioned in our intro

FDA oversight of compounded NAD+ products continues through inspections, recalls, and compliance actions

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