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1,150 rows where agency_id = "FDA" and document_type = "Proposed Rule" sorted by posted_date descending
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| id | agency_id | docket_id | title | document_type | subtype | posted_date ▲ | posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2023-F-5684-0063 | FDA | Filing of Food Additive Petition from Environmental Defense Fund, et al.; Request to Amend the Food Additive Regulations to Remove the Solvents Benzene, Ethylene Dichloride, Methylene Chloride, and Trichloroethylene FDA-2023-F-5684 | Food Additive Petition From Environmental Defense Fund, et al.; Request To Amend the Food Additive Regulations To Remove the Solvents Benzene, Ethylene Dichloride, Methylene Chloride, and Trichloroethylene; Reopening of the Comment Period | Proposed Rule | Reopening of Comment Period | 2026-05-28T04:00:00Z | 2026 | 5 | 2026-05-28T04:00:00Z | 2026-05-28T17:35:28Z | 2026-10615 | 0 | 0 | 09000064b92f8742 | |
| FDA-2023-C-5679-0036 | FDA | Filing of Color Additive Petition from Environmental Defense Fund, et al.; Request to Amend the Color Additive Regulations to Remove the Solvents Ethylene Dichloride, Methylene Chloride, and Trichloroethylene FDA-2023-C-5679 | Color Additive Petition from Environmental Defense Fund, et al.; Request To Amend the Color Additive Regulations To Remove the Solvents Ethylene Dichloride, Methylene Chloride, and Trichloroethylene; Reopening of the Comment Period | Proposed Rule | Reopening of Comment Period | 2026-05-28T04:00:00Z | 2026 | 5 | 2026-05-28T04:00:00Z | 2026-05-28T17:27:49Z | 2026-10614 | 0 | 0 | 09000064b92f881c | |
| FDA-2026-C-3071-0001 | FDA | Filing of Color Additive Petition from the International Association of Color Manufacturers; Request to Amend the Color Additive Regulations to Remove the Solvents Methylene Chloride, Trichloroethylene, and Ethylene Dichloride FDA-2026-C-3071 | Filing of Color Additive Petition: International Association of Color Manufacturers; Request to Amend the Color Additive Regulations to Remove the Solvents Methylene Chloride, Trichloroethylene, and Ethylene Dichloride | Proposed Rule | Petition | 2026-04-01T04:00:00Z | 2026 | 4 | 2026-04-01T04:00:00Z | 2026-06-02T03:59:59Z | 2026-05-28T09:00:14Z | 2026-06295 | 0 | 0 | 09000064b9249960 |
| FDA-2026-N-2590-0001 | FDA | Microbiology Devices; Reclassification of Mycobacterium tuberculosis Cell-Mediated Immunity Tests and Immune Response Enzyme-Linked Immunospot Tests FDA-2026-N-2590 | Microbiology Devices; Reclassification of Mycobacterium Tuberculosis Cell-Mediated Immunity Tests and Immune Response Enzyme-Linked Immunospot Tests | Proposed Rule | Request for Comment | 2026-03-30T04:00:00Z | 2026 | 3 | 2026-03-30T04:00:00Z | 2026-05-30T03:59:59Z | 2026-05-30T09:00:24Z | 2026-06064 | 0 | 0 | 09000064b92437b6 |
| FDA-2025-N-5995-0001 | FDA | Effective Date of Requirement for Premarket Approval Applications for Blood Irradiators Intended to Prevent Metastasis FDA-2025-N-5995 | Effective Date of Requirement for Premarket Approval Applications for Blood Irradiators Intended To Prevent Metastasis | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2026-03-18T04:00:00Z | 2026 | 3 | 2026-03-18T04:00:00Z | 2026-05-19T03:59:59Z | 2026-05-19T09:00:11Z | 2026-05322 | 0 | 0 | 09000064b92215cb |
| FDA-2025-N-5996-0001 | FDA | Medical Devices; Radiology Devices; Classification of Blood Irradiators FDA-2025-N-5996 | Medical Devices; Radiology Devices; Classification of Blood Irradiators | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2026-03-18T04:00:00Z | 2026 | 3 | 2026-03-18T04:00:00Z | 2026-05-19T03:59:59Z | 2026-05-19T09:00:12Z | 2026-05320 | 0 | 0 | 09000064b92216a5 |
| FDA-2015-N-1765-8195 | FDA | General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products FDA-2015-N-1765 | General and Plastic Surgery Devices: Restricted Sale, Distribution, and Use of Sunlamp Products; Withdrawal of Proposed Rule | Proposed Rule | Withdrawal | 2026-03-16T04:00:00Z | 2026 | 3 | 2026-03-16T17:21:55Z | 2026-05103 | 0 | 0 | 09000064b9219c27 | ||
| FDA-2026-C-2014-0001 | FDA | Ecoflora Cares; Filing of Color Additive Petition FDA-2026-C-2014 | Ecoflora Cares; Filing of Color Additive Petition | Proposed Rule | Petition | 2026-03-04T05:00:00Z | 2026 | 3 | 2026-03-04T05:00:00Z | 2026-03-04T20:17:15Z | 2026-04288 | 0 | 0 | 09000064b91eefa8 | |
| FDA-2026-F-2048-0001 | FDA | Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use) FDA-2026-F-2048 | Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2026-03-04T05:00:00Z | 2026 | 3 | 2026-03-04T05:00:00Z | 2026-04-04T03:59:59Z | 2026-03-24T09:00:27Z | 2026-04284 | 0 | 0 | 09000064b91ef081 |
| FDA-1991-N-0191-0001 | FDA | Civil money penalties:biologics, drugs and medical devices FDA-1991-N-0191 | CIVIL MONEY PENALTIES: BIOLOGICS, DRUGS, AND MEDICAL DEVICES | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2026-02-27T05:00:00Z | 2026 | 2 | 2026-02-27T05:00:00Z | 1993-07-27T03:59:59Z | 2026-02-28T01:41:45Z | 93-12314 | 0 | 0 | 090000648052de75 |
| FDA-2023-N-4225-0133 | FDA | Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products FDA-2023-N-4225 | Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products; Withdrawal | Proposed Rule | Withdrawal | 2025-11-28T05:00:00Z | 2025 | 11 | 2025-11-28T05:00:00Z | 2025-11-28T19:47:58Z | 2025-21407 | 0 | 0 | 09000064b90a1ed0 | |
| FDA-2025-F-6173-0001 | FDA | Green Innovation GmbH; Filing of Food Additive Petition (Animal Use) FDA-2025-F-6173 | Green Innovation GmbH; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2025-11-26T05:00:00Z | 2025 | 11 | 2025-11-26T19:23:46Z | 2025-21226 | 0 | 0 | 09000064b909e9fc | ||
| FDA-2025-N-4622-0001 | FDA | Immunology and Microbiology Devices; Reclassification of Nucleic Acid-Based Test Systems for Use with a Corresponding Approved Oncology Therapeutic Product FDA-2025-N-4622 | Immunology and Microbiology Devices; Reclassification of Nucleic Acid-Based Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product; Proposed Amendment; Proposed Order; Request for Comments | Proposed Rule | Request for Comment | 2025-11-25T05:00:00Z | 2025 | 11 | 2025-11-25T05:00:00Z | 2026-01-27T04:59:59Z | 2026-01-31T13:10:53Z | 2025-21071 | 0 | 0 | 09000064b9098c69 |
| FDA-2025-C-3543-0001 | FDA | Proposal to Remove the Color Additive Listing for Use of Orange B on Casings or Surfaces of Frankfurters and Sausages FDA-2025-C-3543 | Proposal To Remove the Color Additive Listing for Use of Orange B on Casings or Surfaces of Frankfurters and Sausages | Proposed Rule | Amendment | 2025-09-17T04:00:00Z | 2025 | 9 | 2025-09-17T04:00:00Z | 2025-10-18T03:59:59Z | 2025-10-16T09:00:27Z | 2025-18023 | 0 | 0 | 09000064b8fa6149 |
| FDA-2025-F-3179-0001 | FDA | Biomin GmbH; Filing of Food Additive Petition (Animal Use) FDA-2025-F-3179 | Biomin GmbH; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2025-09-03T04:00:00Z | 2025 | 9 | 2025-09-03T04:00:00Z | 2025-09-03T18:20:13Z | 2025-16859 | 0 | 0 | 09000064b8f32933 | |
| FDA-2025-F-3070-0001 | FDA | Evonik Corporation; Filing of Food Additive Petition (Animal Use) FDA-2025-F-3070 | Evonik Corporation; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2025-08-19T04:00:00Z | 2025 | 8 | 2025-08-19T04:00:00Z | 2025-08-19T16:25:10Z | 2025-15792 | 0 | 0 | 09000064b8f0711c | |
| FDA-2022-P-1668-0035 | FDA | Request that the FDA amend the standard of identity for Pasteurized Orange Juice to reduce the minimum Brix level FDA-2022-P-1668 | Food Standards of Identity Modernization; Pasteurized Orange Juice; Proposed Rule; Correction | Proposed Rule | Correction | 2025-08-14T04:00:00Z | 2025 | 8 | 2025-08-14T04:00:00Z | 2025-08-14T16:38:08Z | 2025-15473 | 0 | 0 | 09000064b8efd9ce | |
| FDA-2014-N-0053-1330 | FDA | Designation of High-Risk Foods for Tracing; Request for Comments and for Scientific Data and Information FDA-2014-N-0053 | Requirements for Additional Traceability Records for Certain Foods: Compliance Date Extension | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-08-07T04:00:00Z | 2025 | 8 | 2025-08-07T04:00:00Z | 2025-09-09T03:59:59Z | 2025-09-11T09:00:20Z | 2025-14967 | 0 | 0 | 09000064b8eec2b5 |
| FDA-2022-P-1668-0016 | FDA | Request that the FDA amend the standard of identity for Pasteurized Orange Juice to reduce the minimum Brix level FDA-2022-P-1668 | Food Standards of Identity Modernization; Pasteurized Orange Juice | Proposed Rule | Request for Comment | 2025-08-06T04:00:00Z | 2025 | 8 | 2025-08-06T04:00:00Z | 2025-11-05T04:59:59Z | 2025-11-07T10:00:06Z | 2025-14949 | 0 | 0 | 09000064b8ee592e |
| FDA-2025-F-2423-0001 | FDA | APIX Biosciences US LLC; Filing of Food Additive Petition (Animal Use) FDA-2025-F-2423 | APIX Biosciences US LLC; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2025-07-29T04:00:00Z | 2025 | 7 | 2025-07-29T04:00:00Z | 2025-07-29T16:28:33Z | 2025-14335 | 0 | 0 | 09000064b8eb6a13 | |
| FDA-2025-F-2137-0001 | FDA | Spoonbill Foundation; Filing of Food Additive Petition FDA-2025-F-2137 | Spoonbill Foundation; Filing of Food Additive Petition | Proposed Rule | Petition | 2025-07-29T04:00:00Z | 2025 | 7 | 2025-07-29T04:00:00Z | 2025-07-29T16:53:39Z | 2025-14339 | 0 | 0 | 09000064b8eb69a0 | |
| FDA-2025-N-1307-0001 | FDA | Proposal to Revoke 23 Standards of Identity for Foods FDA-2025-N-1307 | Proposal to Revoke 23 Standards of Identity for Foods | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-07-17T04:00:00Z | 2025 | 7 | 2025-07-17T04:00:00Z | 2025-09-16T03:59:59Z | 2025-09-16T09:00:28Z | 2025-13420 | 0 | 0 | 09000064b8e7edb6 |
| FDA-2025-N-1184-0001 | FDA | Revocation of Food Standards for 11 Products Not Currently Sold FDA-2025-N-1184 | Revocation of Food Standards for 11 Products Not Currently Sold | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-07-17T04:00:00Z | 2025 | 7 | 2025-07-17T04:00:00Z | 2025-08-19T03:59:59Z | 2025-08-02T09:00:21Z | 2025-13423 | 0 | 0 | 09000064b8e7ef53 |
| FDA-2025-N-1225-0001 | FDA | Proposal to Revoke 21 Standards of Identity for Dairy Products FDA-2025-N-1225 | Proposal to Revoke 18 Standards of Identity for Dairy Products | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-07-17T04:00:00Z | 2025 | 7 | 2025-07-17T04:00:00Z | 2025-09-16T03:59:59Z | 2025-09-16T09:00:28Z | 2025-13424 | 0 | 0 | 09000064b8e7ee89 |
| FDA-2025-N-1243-0001 | FDA | Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use with a Corresponding Approved Oncology Therapeutic Product FDA-2025-N-1243 | Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product | Proposed Rule | Request for Comment | 2025-06-11T04:00:00Z | 2025 | 6 | 2025-06-11T04:00:00Z | 2025-08-12T03:59:59Z | 2025-08-12T09:00:21Z | 2025-10549 | 0 | 0 | 09000064b8ded24e |
| FDA-2024-D-2604-0059 | FDA | Establishing Sanitation Programs for Low-Moisture Ready-to-Eat Human Foods and Taking Corrective Actions Following a Pathogen Contamination Event; Draft Guidance for Industry; Availability FDA-2024-D-2604 | Establishing Sanitation Programs for Low-Moisture Ready-to-Eat Human Foods and Taking Corrective Actions Following a Pathogen Contamination Event: Draft Guidance for Industry; Reopening of Comment Period | Proposed Rule | Reopening of Comment Period | 2025-05-29T00:00:00Z | 2025 | 5 | 2025-05-29T00:00:00Z | 2025-05-29T18:20:10Z | 2025-09653 | 0 | 0 | 09000064b8dc7731 | |
| FDA-2024-N-2910-4124 | FDA | Food Labeling: Front-of-Package Nutrition Information FDA-2024-N-2910 | Food Labeling: Front-of-Package Nutrition Information; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2025-05-09T00:00:00Z | 2025 | 5 | 2025-05-09T00:00:00Z | 2025-05-21T19:36:24Z | 2025-08204 | 0 | 0 | 09000064b8d1fe08 | |
| FDA-2025-C-0380-0001 | FDA | Impossible Foods, Inc.; Filing of Color Additive Petition FDA-2025-C-0380 | Impossible Foods, Inc.; Filing of Color Additive Petition | Proposed Rule | Petition | 2025-03-14T04:00:00Z | 2025 | 3 | 2025-03-14T04:00:00Z | 2025-03-14T12:47:30Z | 2025-04034 | 0 | 0 | 09000064869f02ca | |
| FDA-2024-N-2910-0001 | FDA | Food Labeling: Front-of-Package Nutrition Information FDA-2024-N-2910 | Food Labeling: Front-of-Package Nutrition Information | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-01-16T05:00:00Z | 2025 | 1 | 2025-01-16T05:00:00Z | 2025-07-16T03:59:59Z | 2025-09-06T09:00:11Z | 2025-00778 | 0 | 0 | 09000064868c5a35 |
| FDA-2024-N-5471-0001 | FDA | Tobacco Product Standard for Nicotine Yield of Cigarettes and Certain Other Combusted FDA-2024-N-5471 | Tobacco Product Standard for Nicotine Yield of Cigarettes and Certain Other Combusted Tobacco Products | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-01-16T05:00:00Z | 2025 | 1 | 2025-01-16T05:00:00Z | 2025-09-16T03:59:59Z | 2025-09-18T09:00:20Z | 2025-00397 | 0 | 0 | 09000064868c5f95 |
| FDA-2024-D-2604-0001 | FDA | Establishing Sanitation Programs for Low-Moisture Ready-to-Eat Human Foods and Taking Corrective Actions Following a Pathogen Contamination Event; Draft Guidance for Industry; Availability FDA-2024-D-2604 | Establishing Sanitation Programs for Low-Moisture Ready-To-Eat Human Foods and Taking Corrective Actions Following a Pathogen Contamination Event; Draft Guidance for Industry; Availability | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2025-01-07T00:00:00Z | 2025 | 1 | 2025-05-29T18:19:55Z | 2024-31528 | 0 | 0 | 09000064868a34d4 | ||
| FDA-2023-N-4225-0001 | FDA | Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products FDA-2023-N-4225 | Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2024-12-27T05:00:00Z | 2024 | 12 | 2024-12-27T05:00:00Z | 2025-03-28T03:59:59Z | 2025-03-29T01:00:19Z | 2024-30544 | 0 | 0 | 090000648689150a |
| FDA-2024-F-5640-0001 | FDA | Monterey Mushrooms, LLC; Filing of Food Additive Petition FDA-2024-F-5640 | Monterey Mushrooms, LLC; Filing of Food Additive Petition | Proposed Rule | Petition | 2024-12-26T05:00:00Z | 2024 | 12 | 2024-12-26T05:00:00Z | 2024-12-26T15:35:48Z | 2024-30362 | 0 | 0 | 090000648688c059 | |
| FDA-2024-F-5467-0001 | FDA | Leprino Nutrition; Filing of Food Additive Petition FDA-2024-F-5467 | Leprino Nutrition; Filing of Food Additive Petition | Proposed Rule | Petition | 2024-12-12T05:00:00Z | 2024 | 12 | 2024-12-12T14:33:28Z | 2024-29248 | 0 | 0 | 09000064868662e0 | ||
| FDA-2016-F-1253-0468 | FDA | Filing of Food Additive Petition: Breast Cancer Fund, Center for Environmental Health, Center for Food Safety, Center for Science In The Public Interest, Clean Water Action, Consumer Federation of America, Earthjustice, Environmental Defense Fund, Improving Kids' Environment, Learning Disabilities Association of America, and Natural Resources Defense Council; Filing of Food Additive Petition FDA-2016-F-1253 | Environmental Defense Fund, et al.; Response to Objections and Requests for a Public Hearing | Proposed Rule | Denial | 2024-10-30T04:00:00Z | 2024 | 10 | 2024-10-30T04:00:00Z | 2024-10-30T13:34:43Z | 2024-25120 | 0 | 0 | 09000064867ebe52 | |
| FDA-2023-F-2319-0004 | FDA | PHM Brands; Filing of Food Additive Petition FDA-2023-F-2319 | PHM Brands; Withdrawal of Food Additive Petition | Proposed Rule | Withdrawal | 2024-09-26T04:00:00Z | 2024 | 9 | 2024-09-26T04:00:00Z | 2024-09-26T13:12:16Z | 2024-21934 | 0 | 0 | 090000648678e405 | |
| FDA-2024-N-3533-0001 | FDA | Microbiology Devices; Reclassification of Antigen, Antibody, and Nucleic Acid-Based Hepatitis B Virus Assay Device FDA-2024-N-3533 | Microbiology Devices; Reclassification of Antigen, Antibody, and Nucleic Acid-Based Hepatitis B Virus Assay Devices | Proposed Rule | Request for Comment | 2024-09-25T04:00:00Z | 2024 | 9 | 2024-09-25T04:00:00Z | 2024-11-26T04:59:59Z | 2024-11-26T02:00:30Z | 2024-21932 | 0 | 0 | 0900006486782c1a |
| FDA-2024-C-4339-0001 | FDA | DSM Biomedical; Filing of Color Additive Petition FDA-2024-C-4339 | DSM Biomedical; Filing of Color Additive Petition | Proposed Rule | Petition | 2024-09-23T04:00:00Z | 2024 | 9 | 2024-09-23T04:00:00Z | 2024-09-23T13:33:12Z | 2024-21684 | 0 | 0 | 0900006486769ff4 | |
| FDA-2024-N-3654-0001 | FDA | Regulatory Hearing Before the Food and Drug Administration; General Provisions; Amendments FDA-2024-N-3654 | Regulatory Hearing Before the Food and Drug Administration; General Provisions; Amendments | Proposed Rule | Amendment | 2024-09-20T04:00:00Z | 2024 | 9 | 2024-09-20T04:00:00Z | 2024-12-05T04:59:59Z | 2024-12-06T02:01:06Z | 2024-21232 | 0 | 0 | 090000648675ecd2 |
| FDA-2024-N-4016-0001 | FDA | Revocation of Regulations Regarding the Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and The European Community FDA-2024-N-4016 | Revocation of Regulations Regarding the Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and The European Community | Proposed Rule | Request for Comment | 2024-09-20T04:00:00Z | 2024 | 9 | 2024-09-20T04:00:00Z | 2024-11-20T04:59:59Z | 2024-11-21T02:00:56Z | 2024-21559 | 0 | 0 | 090000648675ec71 |
| FDA-2024-N-1111-0001 | FDA | Submission of Food and Drug Administration Import Data in the Automated Commercial Environment for Certain Tobacco Products FDA-2024-N-1111 | Submission of Food and Drug Administration Import Data in the Automated Commercial Environment for Certain Tobacco Products | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2024-08-16T04:00:00Z | 2024 | 8 | 2024-08-16T04:00:00Z | 2024-10-16T03:59:59Z | 2024-10-17T01:01:14Z | 2024-18343 | 0 | 0 | 090000648664dc6c |
| FDA-2024-D-2977-0001 | FDA | FDA Enforcement Policy for AAFCO-Defined Animal Feed Ingredients; Draft Guidance for Industry; Availability FDA-2024-D-2977 | Food and Drug Administration Enforcement Policy for Association of American Feed Control Officials— Defined Animal Feed Ingredients; Draft Guidance for Industry; Availability | Proposed Rule | GDL Guidance | 2024-08-09T04:00:00Z | 2024 | 8 | 2024-08-09T04:00:00Z | 2024-08-19T14:37:03Z | 2024-17781 | 0 | 0 | 090000648662856d | |
| FDA-2024-C-3384-0001 | FDA | GNT USA, LLC; Filing of Color Additive Petition FDA-2024-C-3384 | GNT USA, LLC; Filing of Color Additive Petition | Proposed Rule | Petition | 2024-08-05T04:00:00Z | 2024 | 8 | 2024-08-05T04:00:00Z | 2024-10-05T03:59:59Z | 2026-02-06T20:14:47Z | 2024-17090 | 0 | 0 | 090000648661bdf1 |
| FDA-2024-F-1912-0019 | FDA | Filing of Food Additive Petition from Environmental Defense Fund, Breast Cancer Prevention Partners, Center for Food Safety, Environmental Working group, Tom Neltner, and Maricel Maffini; Request to Amend the Food Additive Regulations to Remove Authorization of Fluorinated Polyethylene FDA-2024-F-1912 | Filing of Food Additive Petition From Environmental Defense Fund, Breast Cancer Prevention Partners, Center for Food Safety, Environmental Working Group, Tom Neltner, and Maricel Maffini; Request To Amend the Food Additive Regulations To Remove Authorization of Fluorinated Polyethylene; Reopening of the Comment Period; Correction | Proposed Rule | Reopening of Comment Period | 2024-07-25T04:00:00Z | 2024 | 7 | 2024-07-25T04:00:00Z | 2024-07-29T15:28:15Z | 2024-16337 | 0 | 0 | 0900006486605030 | |
| FDA-2024-C-3229-0001 | FDA | Phytolon Ltd.; Filing of Color Additive Petition FDA-2024-C-3229 | Phytolon Ltd.; Filing of Color Additive Petition | Proposed Rule | Petition | 2024-07-18T04:00:00Z | 2024 | 7 | 2024-07-18T14:07:09Z | 2024-15892 | 0 | 0 | 09000064865f8135 | ||
| FDA-2024-N-1939-0001 | FDA | Requirements for Additional Traceability Records for Certain Foods; Proposed Exemption for Cottage Cheese Regulated by the National Conference on Interstate Milk Shipments Grade A Pasteurized Milk Ordinance FDA-2024-N-1939 | Requirements for Additional Traceability Records for Certain Foods; Proposed Exemption for Cottage Cheese Regulated by the National Conference on Interstate Milk Shipments Grade ‘‘A’’ Pasteurized Milk Ordinance | Proposed Rule | Request for Comment | 2024-06-17T04:00:00Z | 2024 | 6 | 2024-06-17T04:00:00Z | 2024-09-17T03:59:59Z | 2024-09-15T01:00:46Z | 2024-13236 | 0 | 0 | 09000064865b9d8c |
| FDA-2016-D-2343-3131 | FDA | Hazard Analysis and Risk-Based Preventive Controls for Human Food FDA-2016-D-2343 | Hazard Analysis and Risk-Based Preventive Controls for Human Food; Draft Guidance for Industry; Appendix 1; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2024-05-31T04:00:00Z | 2024 | 5 | 2024-05-31T04:00:00Z | 2024-05-31T13:19:17Z | 2024-11987 | 0 | 0 | 090000648658e1c0 | |
| FDA-2022-N-1635-0014 | FDA | Color Additive Certification; Increase in Fees for Certification Services FDA-2022-N-1635 | Color Additive Certification; Increase in Fees for Certification Services; Extension of the Comment Period | Proposed Rule | Extension of Comment Period | 2024-05-28T04:00:00Z | 2024 | 5 | 2024-05-28T04:00:00Z | 2024-05-28T16:36:53Z | 2024-11639 | 0 | 0 | 0900006486587641 | |
| FDA-2023-N-5160-0011 | FDA | Labeling Requirements for Approved or Conditionally Approved New Animal Drugs FDA-2023-N-5160 | Labeling Requirements for Approved or Conditionally Approved New Animal Drugs; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2024-05-22T04:00:00Z | 2024 | 5 | 2024-05-22T04:00:00Z | 2024-05-22T15:13:20Z | 2024-11229 | 0 | 0 | 0900006486579492 | |
| FDA-2024-C-2295-0001 | FDA | Lonza Greenwood LLC; Filing of Color Additive Petition FDA-2024-C-2295 | Lonza Greenwood LLC; Filing of Color Additive Petition | Proposed Rule | Petition | 2024-05-17T04:00:00Z | 2024 | 5 | 2024-05-17T04:00:00Z | 2024-05-17T17:02:03Z | 2024-10888 | 0 | 0 | 090000648656bbd5 | |
| FDA-2024-D-0083-0001 | FDA | Enforcement Policy for Certain In Vitro Diagnostic Devices for Immediate Public Health Response in the Absence of a Declaration under Section 564; Draft Guidance for Laboratory Manufacturers and Food and Drug Administration Staff; Availability FDA-2024-D-0083 | Enforcement Policy for Certain In Vitro Diagnostic Devices for Immediate Public Health Response in the Absence of a Declaration Under Section 564; Draft Guidance for Laboratory Manufacturers and Food and Drug Administration Staff; Availability | Proposed Rule | GDL Guidance | 2024-05-06T04:00:00Z | 2024 | 5 | 2024-05-06T04:00:00Z | 2024-05-06T14:30:21Z | 2024-08934 | 0 | 0 | 09000064865425b3 | |
| FDA-2024-F-1912-0001 | FDA | Filing of Food Additive Petition from Environmental Defense Fund, Breast Cancer Prevention Partners, Center for Food Safety, Environmental Working group, Tom Neltner, and Maricel Maffini; Request to Amend the Food Additive Regulations to Remove Authorization of Fluorinated Polyethylene FDA-2024-F-1912 | Filing of Food Additive Petition From Environmental Defense Fund, Breast Cancer Prevention Partners, Center for Food Safety, Environmental Working Group, Tom Neltner, and Maricel Maffini; Request To Amend the Food Additive Regulations To Remove Authorization of Fluorinated Polyethylene | Proposed Rule | Petition | 2024-04-26T04:00:00Z | 2024 | 4 | 2024-04-26T04:00:00Z | 2024-09-24T03:59:59Z | 2024-09-24T01:01:08Z | 2024-09027 | 0 | 0 | 09000064864f275e |
| FDA-2022-N-1635-0008 | FDA | Color Additive Certification; Increase in Fees for Certification Services FDA-2022-N-1635 | Color Additive Certification; Increase in Fees for Certification Services; Reopening of the Comment Period | Proposed Rule | Reopening of Comment Period | 2024-04-26T04:00:00Z | 2024 | 4 | 2024-04-26T04:00:00Z | 2024-06-28T03:59:59Z | 2024-06-28T01:00:42Z | 2024-08950 | 0 | 0 | 09000064864f28cf |
| FDA-2023-N-3902-0001 | FDA | Banned Devices; Proposal to Ban Electrical Stimulation Devices for Self-Injurious or Aggressive Behavior Center: Center for Devices and Radiological Health FDA-2023-N-3902 | Banned Devices; Proposal To Ban Electrical Stimulation Devices for Self- Injurious or Aggressive Behavior | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2024-03-26T04:00:00Z | 2024 | 3 | 2024-03-26T04:00:00Z | 2024-05-29T03:59:59Z | 2024-06-29T01:00:33Z | 2024-06037 | 0 | 0 | 0900006486498a82 |
| FDA-2023-N-0061-0001 | FDA | Drug Products or Categories of Drug Products That Present Demonstrable Difficulties for Compounding Under Sections 503A or 503B of the Federal Food, Drug, and Cosmetic Act FDA-2023-N-0061 | Drug Products or Categories of Drug Products That Present Demonstrable Difficulties for Compounding Under Sections 503A or 503B of the Federal Food, Drug, and Cosmetic Act | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2024-03-20T04:00:00Z | 2024 | 3 | 2024-03-20T04:00:00Z | 2024-06-19T03:59:59Z | 2024-06-20T01:00:32Z | 2024-05801 | 0 | 0 | 090000648648745b |
| FDA-2024-C-1085-0001 | FDA | Phytolon Ltd; Filing of Color Additive Petition FDA-2024-C-1085 | Filing of Color Additive Petition From Phytolon Ltd. | Proposed Rule | Petition | 2024-03-12T04:00:00Z | 2024 | 3 | 2024-03-12T04:00:00Z | 2026-02-06T20:44:21Z | 2024-05216 | 0 | 0 | 09000064864747b7 | |
| FDA-2023-N-5160-0001 | FDA | Labeling Requirements for Approved or Conditionally Approved New Animal Drugs FDA-2023-N-5160 | Labeling Requirements for Approved or Conditionally Approved New Animal Drugs | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2024-03-12T04:00:00Z | 2024 | 3 | 2024-03-12T04:00:00Z | 2024-08-10T03:59:59Z | 2024-08-10T01:01:02Z | 2024-04840 | 0 | 0 | 090000648647460c |
| FDA-2022-D-2997-0001 | FDA | Key Information and Facilitating Understanding in Informed Consent for FDA-Regulated Clinical Investigations; Draft Guidance for Sponsors, Clinical Investigators, and Institutional Review Boards; Availability FDA-2022-D-2997 | Key Information and Facilitating Understanding in Informed Consent; Draft Guidance for Sponsors, Investigators, and Institutional Review Boards; Availability | Proposed Rule | GDL Guidance | 2024-03-01T05:00:00Z | 2024 | 3 | 2024-03-01T05:00:00Z | 2024-03-01T16:26:43Z | 2024-04377 | 0 | 0 | 0900006486448247 | |
| FDA-2016-D-2343-0090 | FDA | Hazard Analysis and Risk-Based Preventive Controls for Human Food FDA-2016-D-2343 | Hazard Analysis and Risk-Based Preventive Controls for Human Food; Draft Guidance for Industry; Availability | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2024-02-02T05:00:00Z | 2024 | 2 | 2024-05-31T13:17:55Z | 2024-01911 | 0 | 0 | 09000064863d7b13 | ||
| FDA-2023-C-5679-0001 | FDA | Filing of Color Additive Petition from Environmental Defense Fund, et al.; Request to Amend the Color Additive Regulations to Remove the Solvents Ethylene Dichloride, Methylene Chloride, and Trichloroethylene FDA-2023-C-5679 | Filing of Color Additive Petition From Environmental Defense Fund, et al.; Request To Amend the Color Additive Regulations To Remove the Solvents Ethylene Dichloride, Methylene Chloride, and Trichloroethylene | Proposed Rule | Petition | 2024-01-11T05:00:00Z | 2024 | 1 | 2024-01-11T05:00:00Z | 2024-03-12T03:59:59Z | 2024-03-12T01:02:14Z | 2024-00410 | 0 | 0 | 0900006486392343 |
| FDA-2023-F-5684-0001 | FDA | Filing of Food Additive Petition from Environmental Defense Fund, et al.; Request to Amend the Food Additive Regulations to Remove the Solvents Benzene, Ethylene Dichloride, Methylene Chloride, and Trichloroethylene FDA-2023-F-5684 | Filing of Food Additive Petition From Environmental Defense Fund, et al.; Request To Amend the Food Additive Regulations To Remove the Solvents Benzene, Ethylene Dichloride, Methylene Chloride, and Trichloroethylene | Proposed Rule | Petition | 2024-01-11T05:00:00Z | 2024 | 1 | 2024-01-11T05:00:00Z | 2024-03-12T03:59:59Z | 2024-05-24T01:00:56Z | 2024-00411 | 0 | 0 | 0900006486392265 |
| FDA-2023-F-5500-0003 | FDA | Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use); Chromium Propionate; Correction FDA-2023-F-5500 | Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2023-12-27T05:00:00Z | 2023 | 12 | 2023-12-27T05:00:00Z | 2023-12-29T15:40:02Z | 2023-15913 | 0 | 0 | 090000648635d670 | |
| FDA-2011-F-0172-2907 | FDA | Nutrition Labeling of Standard Menu Items in Restaurants and Similar Retail Food Establishments FDA-2011-F-0172 | Menu Labeling: Supplemental Guidance for Industry (Edition 2); Draft Guidance for Industry; Availability | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-12-14T05:00:00Z | 2023 | 12 | 2023-12-14T05:00:00Z | 2024-02-13T04:59:59Z | 2024-02-14T02:00:30Z | 2023-27450 | 0 | 0 | 0900006486339900 |
| FDA-2023-N-3392-0001 | FDA | Medical Devices; General and Plastic Surgery Devices; Classification of Certain Solid Wound Dressings, Wound Dressings Formulated as a Gel, Creams, or Ointment, and Liquid Wound Washes FDA-2023-N-3392 | Medical Devices; General and Plastic Surgery Devices; Classification of Certain Solid Wound Dressings; Wound Dressings Formulated as a Gel, Creams, or Ointment; and Liquid Wound Washes | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-11-30T05:00:00Z | 2023 | 11 | 2023-11-30T05:00:00Z | 2024-02-29T04:59:59Z | 2024-03-19T01:03:58Z | 2023-26209 | 0 | 0 | 09000064862c31a9 |
| FDA-2023-N-3275-0001 | FDA | Effective Date of Requirement for Premarket Approval Applications for Certain Solid Wound Dressings, Wound Dressings Formulated as a Gel, Cream, or Ointment, and Liquid Wound Washes Containing Medically Important Antimicrobials FDA-2023-N-3275 | Effective Date of Requirement for Premarket Approval Applications for Certain Solid Wound Dressings; Wound Dressings Formulated as a Gel, Cream, or Ointment; and Liquid Wound Washes Containing Medically Important Antimicrobials | Proposed Rule | Amendment | 2023-11-30T05:00:00Z | 2023 | 11 | 2023-11-30T05:00:00Z | 2024-02-29T04:59:59Z | 2024-02-29T02:00:22Z | 2023-26208 | 0 | 0 | 09000064862c3354 |
| FDA-2023-N-0937-0001 | FDA | Revocation of Authorization for Use of Brominated Vegetable Oil in Food FDA-2023-N-0937 | Revocation of Authorization for Use of Brominated Vegetable Oil in Food | Proposed Rule | Supplemental Notice of Proposed Rulemaking (SNPRM) | 2023-11-03T04:00:00Z | 2023 | 11 | 2023-11-03T04:00:00Z | 2024-01-18T04:59:59Z | 2024-03-11T16:49:19Z | 2023-24084 | 0 | 0 | 09000064861df978 |
| FDA-2011-N-0179-0034 | FDA | Information Required in Prior Notice of Imported Food FDA-2011-N-0179 | Prior Notice: Adding Requirement to Submit Mail Tracking Number for Articles of Food Arriving by International Mail and Timeframe for Post-Refusal and Post-Hold Submissions | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-11-01T04:00:00Z | 2023 | 11 | 2023-11-01T04:00:00Z | 2024-01-31T04:59:59Z | 2024-02-01T02:00:17Z | 2023-24086 | 0 | 0 | 09000064861bdec9 |
| FDA-2003-F-0321-0003 | FDA | Creamers for Use in Alcoholic Beverages FDA-2003-F-0321 | Kerry Inc.; Filing of Food Additive Petition | Proposed Rule | Petition | 2023-10-13T04:00:00Z | 2023 | 10 | 2023-10-13T04:00:00Z | 2023-10-13T13:16:03Z | 2023-22637 | 0 | 0 | 09000064860cdca8 | |
| FDA-2023-F-4332-0001 | FDA | Kerry Inc.; Filing of Food Additive Petition FDA-2023-F-4332 | Kerry Ingredients and Flavours Ltd.; Filing of Food Additive Petition | Proposed Rule | Petition | 2023-10-13T04:00:00Z | 2023 | 10 | 2023-10-13T04:00:00Z | 2023-10-13T13:20:34Z | 2023-22613 | 0 | 0 | 09000064860cdcee | |
| FDA-2023-N-2177-0001 | FDA | Medical Devices; Laboratory Developed Tests FDA-2023-N-2177 | Medical Devices; Laboratory Developed Tests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-10-03T04:00:00Z | 2023 | 10 | 2023-10-03T04:00:00Z | 2023-12-05T04:59:59Z | 2023-12-15T02:01:05Z | 2023-21662 | 0 | 0 | 09000064860248ba |
| FDA-2013-N-0227-0359 | FDA | Tobacco Product Manufacturing Practice; Establishment of a Public Docket FDA-2013-N-0227 | Proposed Requirements for Tobacco Product Manufacturing Practice; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2023-08-29T04:00:00Z | 2023 | 8 | 2023-08-29T04:00:00Z | 2023-08-29T14:06:31Z | 2023-18625 | 0 | 0 | 0900006485f09717 | |
| FDA-2016-P-0147-0009 | FDA | Petitioner requests that the FDA amend regulations in accordance with the initiatives set forth in this petition. FDA-2016-P-0147 | Fish and Shellfish; Canned Tuna Standard of Identity and Standard of Fill of Container | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-08-25T04:00:00Z | 2023 | 8 | 2023-08-25T04:00:00Z | 2023-11-25T04:59:59Z | 2023-11-25T02:04:25Z | 2023-17916 | 0 | 0 | 0900006485eea43b |
| FDA-2023-N-2632-0001 | FDA | Food Standards of Identity Modernization; Pasteurized Orange Juice; Request for Information FDA-2023-N-2632 | Food Standards of Identity Modernization; Pasteurized Orange Juice; Request for Information | Proposed Rule | Request for Information | 2023-08-16T04:00:00Z | 2023 | 8 | 2023-08-16T04:00:00Z | 2023-10-17T03:59:59Z | 2023-10-17T01:04:05Z | 2023-17453 | 0 | 0 | 0900006485e54476 |
| FDA-2019-N-4750-0001 | FDA | Revocation of Uses of Partially Hydrogenated Oils in Foods FDA-2019-N-4750 | Revocation of Uses of Partially Hydrogenated Oils in Foods; Companion Document to Direct Final Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-08-09T04:00:00Z | 2023 | 8 | 2023-08-09T04:00:00Z | 2023-10-24T03:59:59Z | 2023-10-24T01:03:11Z | 2023-16724 | 0 | 0 | 0900006485e046fb |
| FDA-2023-C-1487-0013 | FDA | Filing of Color Additive Petition From Environmental Defense Fund, et al.; Request To Revoke Color Additive Listing for Use of Titanium Dioxide in Food FDA-2023-C-1487 | Filing of Color Additive Petition From Environmental Defense Fund, et al.; Request To Revoke Color Additive Listing for Use of Titanium Dioxide in Food; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2023-06-28T04:00:00Z | 2023 | 6 | 2023-06-28T04:00:00Z | 2023-09-02T03:59:59Z | 2023-09-02T01:01:15Z | 2023-13773 | 0 | 0 | 0900006485c04ee7 |
| FDA-2023-F-2415-0001 | FDA | Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use) FDA-2023-F-2415 | Kemin Industries, Inc.; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2023-06-27T04:00:00Z | 2023 | 6 | 2023-06-27T04:00:00Z | 2023-06-27T13:48:37Z | 2023-13545 | 0 | 0 | 0900006485bfd0c6 | |
| FDA-2023-F-2319-0001 | FDA | PHM Brands; Filing of Food Additive Petition FDA-2023-F-2319 | PHM Brands; Filing of Food Additive Petition | Proposed Rule | Petition | 2023-06-21T04:00:00Z | 2023 | 6 | 2023-06-21T04:00:00Z | 2023-07-22T03:59:59Z | 2024-09-26T13:12:04Z | 2023-13120 | 0 | 0 | 0900006485b9161f |
| FDA-2019-N-5959-0001 | FDA | Medication Guides: Patient Medication Information; Proposed Rule FDA-2019-N-5959 | Medication Guides: Patient Medication Information | Proposed Rule | Amendment | 2023-05-31T04:00:00Z | 2023 | 5 | 2023-05-31T04:00:00Z | 2023-11-28T04:59:59Z | 2024-09-05T01:00:43Z | 2023-11354 | 0 | 0 | 0900006485a9510f |
| FDA-2023-C-1487-0003 | FDA | Filing of Color Additive Petition From Environmental Defense Fund, et al.; Request To Revoke Color Additive Listing for Use of Titanium Dioxide in Food FDA-2023-C-1487 | Filing of Color Additive Petition From Environmental Defense Fund, et al.; Request To Revoke Color Additive Listing for Use of Titanium Dioxide in Food | Proposed Rule | Petition | 2023-05-03T04:00:00Z | 2023 | 5 | 2023-05-03T04:00:00Z | 2023-09-02T03:59:59Z | 2023-09-02T01:04:20Z | 2023-09366 | 0 | 0 | 09000064859c16ca |
| FDA-2022-N-2226-0001 | FDA | Use of Salt Substitutes to Reduce the Sodium Content in Standardized Foods FDA-2022-N-2226 | Use of Salt Substitutes To Reduce the Sodium Content in Standardized Foods | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-04-10T04:00:00Z | 2023 | 4 | 2023-04-10T04:00:00Z | 2023-08-09T03:59:59Z | 2023-08-18T01:02:51Z | 2023-06456 | 0 | 0 | 090000648591b92d |
| FDA-2023-N-0437-5004 | FDA | Filing of Color Additive Petition from Center for Science in the Public Interest, et al.; Request to Revoke Color Additive Listing for Use of FD&C Red No. 3 in Food and Ingested Drugs. FDA-2023-N-0437 | Filing of Color Additive Petition From Center for Science in the Public Interest, et al.; Request To Revoke Color Additive Listing for Use of FD&C Red No. 3 in Food and Ingested Drugs; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2023-03-30T04:00:00Z | 2023 | 3 | 2023-03-30T04:00:00Z | 2023-06-05T21:42:29Z | 2023-06579 | 0 | 0 | 0900006485892879 | |
| FDA-2013-N-0227-0067 | FDA | Tobacco Product Manufacturing Practice; Establishment of a Public Docket FDA-2013-N-0227 | Proposed Requirements for Tobacco Product Manufacturing Practice; Public Hearing; Request for Comments | Proposed Rule | Request for Comment | 2023-03-10T05:00:00Z | 2023 | 3 | 2023-03-10T05:00:00Z | 2023-09-07T03:59:59Z | 2023-10-21T01:00:27Z | 2023-04592 | 0 | 0 | 090000648578c58b |
| FDA-2013-N-0227-0068 | FDA | Tobacco Product Manufacturing Practice; Establishment of a Public Docket FDA-2013-N-0227 | Proposed Requirements for Tobacco Products Manufacturing Practice; Tobacco Products Scientific Advisory Committee; Notice of Meeting; Request for Comments | Proposed Rule | Request for Comment | 2023-03-10T05:00:00Z | 2023 | 3 | 2023-03-10T05:00:00Z | 2023-05-12T03:59:59Z | 2023-05-12T01:00:43Z | 2023-04593 | 0 | 0 | 090000648578c5c6 |
| FDA-2013-N-0227-0066 | FDA | Tobacco Product Manufacturing Practice; Establishment of a Public Docket FDA-2013-N-0227 | Requirements for Tobacco Product Manufacturing Practice | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2023-03-10T05:00:00Z | 2023 | 3 | 2023-03-10T05:00:00Z | 2023-10-07T03:59:59Z | 2023-11-03T01:03:25Z | 2023-04591 | 0 | 0 | 090000648578b4f7 |
| FDA-1995-N-0062-0196 | FDA | Quality/fill Container; Common or Unusual Name Regulations FDA-1995-N-0062 | Food Standards; General Principles and Food Standards Modernization; Withdrawal of Proposed Rule | Proposed Rule | Withdrawal | 2023-03-01T05:00:00Z | 2023 | 3 | 2023-03-01T05:00:00Z | 2023-03-01T16:19:21Z | 2023-04114 | 0 | 0 | 09000064857323da | |
| FDA-2023-C-0544-0001 | FDA | Innophos, Inc.; Filing of Color Additive Petition FDA-2023-C-0544 | Innophos, Inc.; Filing of Color Additive Petition | Proposed Rule | Petition | 2023-02-27T05:00:00Z | 2023 | 2 | 2023-02-27T05:00:00Z | 2023-02-27T19:06:34Z | 2023-03955 | 0 | 0 | 090000648571b8c0 | |
| FDA-2023-N-0437-0001 | FDA | Filing of Color Additive Petition from Center for Science in the Public Interest, et al.; Request to Revoke Color Additive Listing for Use of FD&C Red No. 3 in Food and Ingested Drugs. FDA-2023-N-0437 | Filing of Color Additive Petition From Center for Science in the Public Interest, et al.; Request To Revoke Color Additive Listing for Use of FD&C Red No. 3 in Food and Ingested Drugs | Proposed Rule | Petition | 2023-02-17T05:00:00Z | 2023 | 2 | 2023-02-17T05:00:00Z | 2023-05-19T03:59:59Z | 2023-11-21T02:00:44Z | 2023-03391 | 0 | 0 | 09000064856b6eab |
| FDA-2023-F-0147-0001 | FDA | Micro-Tracers, Inc; Filing of Food Additive Petition FDA-2023-F-0147 | Micro-Tracers, Inc.; Filing of Food Additive Petition | Proposed Rule | Petition | 2023-02-06T05:00:00Z | 2023 | 2 | 2023-02-06T05:00:00Z | 2024-06-07T12:41:04Z | 2023-02449 | 0 | 0 | 0900006485633e2c | |
| FDA-2022-D-0278-0001 | FDA | Action Levels for Lead in Food Intended for Babies and Young Children; Draft Guidance for Industry; Availability FDA-2022-D-0278 | Action Levels for Lead in Food Intended for Babies and Young Children; Draft Guidance for Industry; Availability | Proposed Rule | Advance Notice of Proposed Rulemaking (ANPRM) | 2023-01-25T05:00:00Z | 2023 | 1 | 2023-04-10T15:08:38Z | 2023-01384 | 0 | 0 | 0900006485608b76 | ||
| FDA-2022-N-1635-0005 | FDA | Color Additive Certification; Increase in Fees for Certification Services FDA-2022-N-1635 | Color Additive Certification; Increase in Fees for Certification Services; Reopening of the Comment Period | Proposed Rule | Reopening of Comment Period | 2023-01-24T05:00:00Z | 2023 | 1 | 2023-01-24T05:00:00Z | 2023-01-24T20:20:06Z | 2023-01361 | 0 | 0 | 0900006485605f46 | |
| FDA-2019-N-2650-0001 | FDA | Investigational New Drug Applications; Exemptions for Clinical Investigations to Evaluate a Drug Use of a Product Lawfully Marketed as a Conventional Food, Dietary Supplement, or Cosmetic FDA-2019-N-2650 | Investigational New Drug Applications; Exemptions for Clinical Investigations To Evaluate a Drug Use of a Product Lawfully Marketed as a Conventional Food, Dietary Supplement, or Cosmetic | Proposed Rule | Amendment | 2022-12-09T05:00:00Z | 2022 | 12 | 2022-12-09T05:00:00Z | 2023-03-10T04:59:59Z | 2023-03-11T02:00:26Z | 2022-26728 | 0 | 0 | 090000648552a62c |
| FDA-2020-N-0258-0001 | FDA | Investigational New Drug Application Annual Reporting FDA-2020-N-0258 | Investigational New Drug Application Annual Reporting | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2022-12-09T05:00:00Z | 2022 | 12 | 2022-12-09T05:00:00Z | 2023-03-10T04:59:59Z | 2023-03-31T01:01:11Z | 2022-26731 | 0 | 0 | 090000648552a78a |
| FDA-2016-D-2335-1318 | FDA | Use of the Term “Healthy” in the Labeling of Human Food Products FDA-2016-D-2335 | Food Labeling: Nutrient Content Claims; Definition of Term ‘‘Healthy;’’ Extension of Comment Period | Proposed Rule | Notice of Extension | 2022-11-29T05:00:00Z | 2022 | 11 | 2022-11-29T05:00:00Z | 2022-12-28T15:08:12Z | 2022-26002 | 0 | 0 | 0900006485507b82 | |
| FDA-2022-F-2725-0001 | FDA | Cargill, Incorporated; Filing of Food Additive Petition FDA-2022-F-2725 | Cargill, Inc.; Filing of Food Additive Petition | Proposed Rule | Petition | 2022-11-21T05:00:00Z | 2022 | 11 | 2022-11-21T05:00:00Z | 2022-12-22T04:59:59Z | 2025-09-03T16:25:02Z | 2022-25310 | 0 | 0 | 09000064854f8572 |
| FDA-2019-N-2175-0042 | FDA | Institutional Review Boards; Cooperative Research FDA-2019-N-2175 | Protection of Human Subjects and Institutional Review Boards, and Institutional Review Boards; Cooperative Research; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2022-11-14T05:00:00Z | 2022 | 11 | 2022-11-14T05:00:00Z | 2022-11-28T19:58:49Z | 2022-24689 | 0 | 0 | 09000064854ab725 | |
| FDA-2021-N-0286-0030 | FDA | Part 50 Protection of Human Subjects and Part 56 Institutional Review Boards FDA-2021-N-0286 | Protection of Human Subjects and Institutional Review Boards, and Institutional Review Boards; Cooperative Research; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2022-11-14T05:00:00Z | 2022 | 11 | 2022-11-14T05:00:00Z | 2023-05-20T23:41:26Z | 2022-24689 | 0 | 0 | 09000064854aac1e | |
| FDA-2022-N-1635-0001 | FDA | Color Additive Certification; Increase in Fees for Certification Services FDA-2022-N-1635 | Color Additive Certification; Increase in Fees for Certification Services | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2022-11-02T04:00:00Z | 2022 | 11 | 2022-11-02T04:00:00Z | 2024-05-29T03:59:59Z | 2024-05-29T01:01:00Z | 2022-23844 | 0 | 0 | 090000648547b387 |
| FDA-2022-F-1108-0011 | FDA | Environmental Defense Fund, Maricel Maffini, Breast Cancer Prevention Partners, Clean Water Action/Clean Water Fund, Consumer Reports, Endocrine Society, Environmental Working Group, Healthy Babies Bright Futures, and the Nicholas School of the Environment at Duke University; Filing of Food Additive Petition FDA-2022-F-1108 | Environmental Defense Fund, Maricel Maffini, Breast Cancer Prevention Partners, Clean Water Action/Clean Water Fund, Consumer Reports, Endocrine Society, Environmental Working Group, Healthy Babies Bright Futures, Linda Birnbaum, and the Nicholas School of the Environment at Duke University; Filing of Food Additive Petition; Correction | Proposed Rule | Correction | 2022-10-27T04:00:00Z | 2022 | 10 | 2022-10-27T04:00:00Z | 2024-10-08T15:34:12Z | 2022-23384 | 0 | 0 | 09000064854626b3 | |
| FDA-2021-N-0862-0140 | FDA | Nonprescription Drug Product With an Additional Condition for Nonprescription Use; Proposed Rule FDA-2021-N-0862 | Nonprescription Drug Product With an Additional Condition for Nonprescription Use; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2022-10-24T04:00:00Z | 2022 | 10 | 2022-10-24T04:00:00Z | 2022-11-22T18:58:05Z | 2022-23033 | 0 | 0 | 090000648544cb97 | |
| FDA-2021-N-1348-0001 | FDA | Administrative Destruction of Certain Devices Refused Admission to the United States; Notice of Procedure for Administrative Destruction of Certain Refused Drugs and Devices FDA-2021-N-1348 | Administrative Destruction | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2022-10-07T04:00:00Z | 2022 | 10 | 2022-10-07T04:00:00Z | 2022-12-07T04:59:59Z | 2022-12-07T02:00:33Z | 2022-21809 | 0 | 0 | 09000064853d3855 |
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docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
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posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
open_for_comment INTEGER,
withdrawn INTEGER,
object_id TEXT
);
CREATE INDEX idx_docs_agency ON documents(agency_id);
CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);
CREATE INDEX idx_docs_comment_end ON documents(comment_end_date) WHERE comment_end_date IS NOT NULL AND withdrawn = 0;