{"data":{"id":"us/21-cfr-111.425","jurisdiction":"us","citation":"21 CFR 111.425","heading":"What requirements apply to a packaged and labeled dietary supplement that is rejected for distribution?","body":"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.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION","PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS","Subpart L—Production and Process Control System: Requirements for Packaging and Labeling Operations"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"3f92d9a3a63712e614a8cdf6e2c3b7e21d4183523e72b6b1e45f360caff00922","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-111.420","next":"us/21-cfr-111.430"},"notice":"GroundRules: Original legal text. Not legal advice."}