PART 111 SUBPART G
Subpart G - Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement
- 21 U.S.C. 321, 342, 343, 371, 374, 381, 393; 42 U.S.C. 264.
- 72 FR 34942, June 25, 2007, unless otherwise noted.
|21:184.108.40.206.220.127.116.11||SECTION 111.153||111.153 What are the requirements under this subpart G for written procedures|
|21:18.104.22.168.22.214.171.124||SECTION 111.155||111.155 What requirements apply to components of dietary supplements|
|21:126.96.36.199.188.8.131.52||SECTION 111.160||111.160 What requirements apply to packaging and labels received|
|21:184.108.40.206.220.127.116.11||SECTION 111.165||111.165 What requirements apply to a product received for packaging or labeling as a dietary supplement (and for distribution rather than for return to the supplier)|
|21:18.104.22.168.22.214.171.124||SECTION 111.170||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|
|21:126.96.36.199.188.8.131.52||SECTION 111.180||111.180 Under this subpart G, what records must you make and keep|