21 CFR § 111.425 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.425 What requirements apply to a packaged and labeled dietary supplement that is rejected for distribution?

Current through Sep 8, 2026 · Read all of Part 111

You must clearly identify, hold, and control under a quarantine system for appropriate disposition any packaged and labeled dietary supplement that is rejected for distribution.

← § 111.420 What requirements apply to repackaging and relabeling?§ 111.430 Under this subpart L, what records must you make and keep? →