Code of Federal Regulations (alpha)

CFR /  Title 21  /  Part 111  /  Sec. 111.170 What requirements apply to rejected components, for packaging or labeling as a dietary supplement?

You must clearly identify, hold, and control under a quarantine system for appropriate disposition any component, packaging, and label, and any product that you receive for packaging or labeling as a dietary supplement (and for distribution rather than for return to the supplier), that is rejected and unsuitable for use in manufacturing, packaging, or labeling operations.