§111.420. What requirements apply to repackaging and relabeling?
21 C.F.R. § 111.420
You may repackage or relabel dietary supplements only after quality control personnel have approved such repackaging or relabeling.
You must examine a representative sample of each batch of repackaged or relabeled dietary supplements to determine whether the repackaged or relabeled dietary supplements meet all specifications established in accordance with § 111.70(g).
Quality control personnel must approve or reject each batch of repackaged or relabeled dietary supplement prior to its release for distribution.
Notes, amendments, and revision history
Authority
Authority: 21 U.S.C. 321, 342, 343, 371, 374, 381, 393; 42 U.S.C. 264.
Source
Source: 72 FR 34942, June 25, 2007, unless otherwise noted.