id,agency_id,title,docket_type,last_modified,object_id
FDA-1995-S-0036,FDA,Public Disclosure Materials for Emergency Research Studies Conducted Under 21 CFR 50.24,Rulemaking,2026-02-03T17:37:09Z,0b0000648055af86
FDA-2000-N-0108,FDA,Safety Reporting Requirements Human Drug/Biological Products  - CLOSED,Rulemaking,2025-12-03T18:08:26Z,0b000064804c262a
FDA-2000-N-0011,FDA,Uniform Compliance Date for Food Labeling Regulations,Rulemaking,2025-03-05T10:39:56Z,0b000064804ae7d6
FDA-1978-N-0018,FDA,Sunscreen Drug Products -OPEN,Rulemaking,2025-01-22T08:25:01Z,0b00006480559264
FDA-1975-N-0012,FDA,Health Care Antiseptic Drug Products for Over-the-Counter (OTC) Human Use; CLOSED,Rulemaking,2024-05-24T10:11:19Z,0b000064805c1903
FDA-2006-N-0239,FDA,Index of Legally Marketed Unapproved New Animal Drugs for Minor Species,Rulemaking,2024-05-15T09:29:00Z,0b00006480456e9e
FDA-2003-F-0321,FDA,Creamers for Use in Alcoholic Beverages,Rulemaking,2023-10-13T14:23:03Z,0b00006480495779
FDA-1992-S-0039,FDA,Public Docket to Provide Information on Submissions the Agency is Prepared to Accept Electronically,Rulemaking,2023-07-21T16:50:48Z,0b00006480528808
FDA-2000-P-0126,FDA,Revision of Yogurt Standards,Rulemaking,2023-05-19T08:27:18Z,0b000064804cf4c3
FDA-1998-N-0051,FDA,Over the Counter Human Drugs Labeling Requirements,Rulemaking,2023-04-17T17:42:05Z,0b0000648056e834
FDA-2001-N-0178,FDA,Performance Standard for Diagnostic X-Ray Systems and Their Major Components,Rulemaking,2023-02-22T09:25:21Z,0b000064804e14e6
FDA-1997-N-0020,FDA,Substances Generally Recognized as Safe (GRAS) - Closed,Rulemaking,2022-01-05T01:02:36Z,0b000064805ca0a0
FDA-1975-N-0016,FDA,OTC Topical Antimicrobial Drug Products - OPEN,Rulemaking,2022-01-05T01:02:28Z,0b000064805c1f98
FDA-1975-N-0013,FDA,First Aid; Topical Antimicrobial Drug Products for Over-the-Counter (OTC) Human Use (OPEN),Rulemaking,2022-01-05T01:02:27Z,0b000064805c1d37
FDA-1995-N-0063,FDA,CGMPs for the Production of Infant Formula,Rulemaking,2022-01-05T01:02:26Z,0b0000648056ca61
FDA-2003-N-0196,FDA,Over-the-Counter Drug Products; Safety and Efficacy Review;  Additional Sunscreen Ingredients,Rulemaking,2022-01-05T01:02:18Z,0b0000648048b48b
FDA-2005-N-0345,FDA,"Distribution of Blood Derivatives by Registered Blood Establishments that Qualify as Health Care Entities; Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; Policies, Requirements and Administrative Procedures (Section 610 Review)",Rulemaking,2022-01-05T01:02:18Z,0b00006480449858
FDA-2005-N-0404,FDA,Food Labeling; Gluten-Free Labeling of Foods-CLOSED,Rulemaking,2022-01-05T01:02:18Z,0b0000648044d3d3
FDA-1988-N-0019,FDA,Prescription Drug Marketing Act of 1987,Rulemaking,2022-01-05T01:02:16Z,0b00006480475d46
FDA-1996-N-0006,FDA,Eligibility Criteria for Considering Additional Conditions in the Over-the-Counter Drug Monograph System,Rulemaking,2022-01-05T01:01:55Z,0b000064804f9917
FDA-1992-N-0407,FDA,Prescription Drug Amendments of 1992; Ltr to Regulated Industy,Rulemaking,2022-01-05T01:01:39Z,0b00006480532581
FDA-1977-N-0320,FDA,Protein Supplements-RETIRED,Rulemaking,2021-09-01T18:06:30Z,0b000064805ee043
FDA-1977-N-0259,FDA,"Cultured & Acidified Buttermilk, Yogurts, Milks & Eggnog - OPEN",Rulemaking,2021-09-01T18:06:29Z,0b000064805ed178
FDA-1997-D-0494,FDA,Direct Final Rule Procedures,Rulemaking,2021-09-01T18:06:15Z,0b000064805d46c6
FDA-1980-N-0004,FDA,Over-the-Counter Ophthalmic Drug Products for Emergency First Aid Use; Proposed Amendment of Final Monograph for Over-the-Counter Opthalmic Drug Products,Rulemaking,2021-09-01T18:05:33Z,0b000064805b9002
FDA-1985-C-0553,FDA,Canthaxanthin; Color Additive Exemtp From Ccertification,Rulemaking,2021-09-01T18:05:32Z,0b000064805b7c5a
FDA-1981-N-0293,FDA,"Standards of Identity for Milk, Lowfat Milk & Skim Milk Pasteurized",Rulemaking,2021-09-01T18:05:12Z,0b000064805b0e91
FDA-1981-N-0114,FDA,Topical Acne Drug Product For Over-the-Counter Human Use,Rulemaking,2021-09-01T18:05:07Z,0b000064805b0529
FDA-1978-N-1975,FDA,Red Cell Lysing Reagents -RETIRED,Rulemaking,2021-09-01T18:04:31Z,0b000064805a1aa4
FDA-1978-N-1713,FDA,Blood & Plasma Warming Devices-RETIRED,Rulemaking,2021-09-01T18:04:17Z,0b0000648059cab9
FDA-1978-N-1451,FDA,Blood Cell Diluents-RETIRED,Rulemaking,2021-09-01T18:04:04Z,0b0000648059b436
FDA-1978-N-1463,FDA,Processing Systems for Frozen Blood-RETIRED,Rulemaking,2021-09-01T18:04:04Z,0b0000648059b4f7
FDA-1978-N-1177,FDA,Calibrators for Platelet Counting-RETIRED,Rulemaking,2021-09-01T18:03:42Z,0b000064805984f6
FDA-1978-N-0924,FDA,Thrombin Time Test-RETIRED,Rulemaking,2021-09-01T18:03:29Z,0b0000648058dadc
FDA-1978-N-0925,FDA,Calibrators for Cell Indices-RETIRED,Rulemaking,2021-09-01T18:03:29Z,0b0000648058dbd3
FDA-1998-N-0155,FDA,Treatment of Narcotic Dependence,Rulemaking,2021-09-01T18:03:27Z,0b0000648058b15e
FDA-1978-N-0635,FDA,Empty Containers for the Collection & Processing of Blood-RETIRED,Rulemaking,2021-09-01T18:03:18Z,0b00006480579244
FDA-1978-N-0622,FDA,Calibrators for Red Cell & White Cell Counting,Rulemaking,2021-09-01T18:03:17Z,0b00006480578721
FDA-1978-N-0624,FDA,Medical Devices Classification of Prothrombin-Proconvertin Tests and Thrombotests-RETIRED,Rulemaking,2021-09-01T18:03:17Z,0b0000648057895b
FDA-1978-N-0625,FDA,Partial Thromboplastin Time Tests-RETIRED,Rulemaking,2021-09-01T18:03:17Z,0b00006480578a8f
FDA-1978-N-0632,FDA,Thromboplastin Generation Test-RETIRED,Rulemaking,2021-09-01T18:03:17Z,0b00006480579019
FDA-1978-N-0633,FDA,Automated Blood Grouping & Antibody Test Systems-RETIRED,Rulemaking,2021-09-01T18:03:17Z,0b00006480579087
FDA-1995-N-0259,FDA,Regulations Restricting the Sale & Distribution of Cigarettes & Smokeless Tobacco to Protect Children & Adolescents,Rulemaking,2021-09-01T18:03:13Z,0b00006480571c9d
FDA-1978-N-0375,FDA,Medical Devices Classification of Prothrombin Time Tests-RETIRED,Rulemaking,2021-09-01T18:03:06Z,0b0000648056e729
FDA-1978-N-0379,FDA,Classification of Blood Mixing Devices & Blood Weighing Devices-RETIRED,Rulemaking,2021-09-01T18:03:06Z,0b0000648056e7dd
FDA-1978-N-0380,FDA,Automated Blood Cell Separators-RETIRED,Rulemaking,2021-09-01T18:03:06Z,0b0000648056e7f7
FDA-1978-N-0381,FDA,Automated Cell Washing Centrifuges for Immuno-Hematology-RETIRED,Rulemaking,2021-09-01T18:03:06Z,0b0000648056e829
FDA-1978-N-0382,FDA,Automated Coombs Test Systems-RETIRED,Rulemaking,2021-09-01T18:03:06Z,0b0000648056e83b
FDA-1978-N-0368,FDA,Hematology Stains-RETIRED,Rulemaking,2021-09-01T18:03:05Z,0b0000648056e64a
FDA-1978-N-0123,FDA,Hematology Quality Control Mixtures,Rulemaking,2021-09-01T18:02:55Z,0b00006480564674
FDA-1978-N-0124,FDA,Russell Viper Venom Reagent - RETIRED,Rulemaking,2021-09-01T18:02:55Z,0b00006480564725
FDA-1978-N-0115,FDA,Calibrators for Hemoglobin & Hematocrit Measurement-RETIRED,Rulemaking,2021-09-01T18:02:54Z,0b00006480564113
FDA-1978-N-0061,FDA,Hematology and Pathology Devices Classification of Sickle Cell Tests-RETIRED,Rulemaking,2021-09-01T18:02:53Z,0b000064805622ba
FDA-1978-N-0023,FDA,Skin Bleaching Drug Products- OPEN,Rulemaking,2021-09-01T18:02:51Z,0b0000648055ed99
FDA-1995-G-0034,FDA,Hydrophobic Silica for Animal Feeds-CLOSED,Rulemaking,2021-09-01T18:02:51Z,0b0000648055add9
FDA-1979-N-0424,FDA,Labels of Drug & Cosmetic Products-RETIRED,Rulemaking,2021-09-01T18:02:48Z,0b0000648055648a
FDA-1979-N-0028,FDA,Lakes of Color Additives,Rulemaking,2021-09-01T18:02:36Z,0b0000648055395f
FDA-1992-N-0190,FDA,Standard Identity for Cheese Product FD&C Yellow No. 6 & 5,Rulemaking,2021-09-01T18:02:09Z,0b0000648052f609
FDA-1992-N-0049,FDA,Topical Drug Containing Benzoyl Peroxide; Additional Labeling,Rulemaking,2021-09-01T18:01:56Z,0b0000648052bcdf
FDA-1990-N-0025,FDA,"Food Labeling, Declaration of Ingredients",Rulemaking,2021-09-01T18:01:53Z,0b0000648052957f
FDA-1982-F-0155,FDA,Direct Food Additives: Food Additives Permitted for Direct Addition to Food for Human Consuption; Dimethyl Dicarbonate,Rulemaking,2021-09-01T18:01:19Z,0b0000648050f5f7
FDA-1996-N-0027,FDA,National Environmental Policy Act Proposed Revision of Policies and Procedures,Rulemaking,2021-09-01T18:00:26Z,0b000064804fb548
FDA-2000-N-0044,FDA,Labeling for Human Prescription Drug/Biologic Products-CLOSED,Rulemaking,2021-09-01T02:00:37Z,0b000064804aefdb
FDA-2002-N-0323,FDA,Bioterrorism Preparedness; Registration of Food Facilities,Rulemaking,2021-09-01T01:03:15Z,0b000064804a02e5
FDA-2002-N-0031,FDA,Animal Proteins Prohibited in Ruminant Feed,Rulemaking,2021-09-01T01:02:59Z,0b00006480489512
FDA-2004-N-0188,FDA,BSE Risk Materials in Foods and Cosmetics,Rulemaking,2021-09-01T01:02:13Z,0b000064804702a2
FDA-2006-N-0422,FDA,"Agency Information Collection Activities; Proposed Collection; Comment Request; Irradiation in the Production, Processing, and Handling of Food",Rulemaking,2021-09-01T01:01:38Z,0b00006480461819
FDA-2006-N-0370,FDA,Agency Information Collection Activities; Proposed Collection; Comment Request; Registration of Food Facilities Under the Public Health Security and Bioterrorism Preparedness and Response Act of 2002,Rulemaking,2021-09-01T01:01:37Z,0b0000648045fdf8