{"data":{"id":"us/21-cfr-111.370","jurisdiction":"us","citation":"21 CFR 111.370","heading":"What requirements apply to rejected dietary supplements?","body":"You must clearly identify, hold, and control under a quarantine system for appropriate disposition any dietary supplement that is rejected and unsuitable for use in manufacturing, packaging, or labeling operations.","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 K—Production and Process Control System: Requirements for Manufacturing 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":"1c60fee19babc07d3957dcd11202518d42c912c0ff97a0fdad33250900f53943","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-111.365","next":"us/21-cfr-111.375"},"notice":"GroundRules: Original legal text. Not legal advice."}