{"data":{"id":"us/21-cfr-1.95","jurisdiction":"us","citation":"21 CFR 1.95","heading":"Application for authorization to relabel and recondition.","body":"Application for authorization to relabel or perform other action to bring the article into compliance with the Federal Food, Drug, and Cosmetic Act or to render it other than a food, drug, device, or cosmetic may be filed only by the owner or consignee, and shall:\n(a) Contain detailed proposals for bringing the article into compliance with the act or rendering it other than a food, drug, device, or cosmetic.\n(b) Specify the time and place where such operations will be carried out and the approximate time for their completion.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER A—GENERAL","PART 1—GENERAL ENFORCEMENT REGULATIONS","Subpart E—Imports and Exports"],"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":"4a732e01630a3d61d5f68e7b30c03cf059182154e05f45b4c94dde8409b06cea","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-1.94","next":"us/21-cfr-1.96"},"notice":"GroundRules: Original legal text. Not legal advice."}