Title 21 Part 111 → Subpart G → §111.170

Title 21 → Chapter I → Subchapter B → Part 111 → Subpart G → §111.170

Electronic Code of Federal Regulations e-CFR

§111.170   What requirements apply to rejected components, packaging, and labels, and to rejected products that are received 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.