dockets: FDA-1998-N-0009
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | agency_id | title | docket_type | last_modified | object_id | rin | dkabstract | category | subtype | keywords | program | short_title | effective_date | organization | attrs_raw | attr_source |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-1998-N-0009 | FDA | Definition and Option of Alternative Labeling Requirements for Convenience Size OTC Drug Packages | Nonrulemaking | 2021-09-01T18:02:50Z | 0b00006480558e3e | Docket Status: OPEN | ["OTC Drug Packages", "Convenience-Size", "Requirements", "ALTERNATIVE LABELING", "Option", "Definition", "21 CFR 201.66", "TEA TREE OIL", "EXEMPTION", "READING SAFETY", "ACTIVE INGREDIENTS", "WARNING", "LABELING", "DRUG FACTS", "ASSIST CONSUMERS", "OTC DRUG PRODUCTS", "OPEN"] | CDER | Definition and Option of Alternative Labeling Requirements for Convenience Size OTC Drug Packages | {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "legacyId", "label": "Legacy ID", "tooltip": "A pre-FDMS agency specific identifier migrated from a legacy system."}, {"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}, {"name": "field2", "label": "Docket Status", "tooltip": "Used to Identity that a Docket's Status is Open or Closed"}, {"name": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["OTC Drug Packages", "Convenience-Size", "Requirements", "ALTERNATIVE LABELING", "Option", "Definition", "21 CFR 201.66", "TEA TREE OIL", "EXEMPTION", "READING SAFETY", "ACTIVE INGREDIENTS", "WARNING", "LABELING", "DRUG FACTS", "ASSIST CONSUMERS", "OTC DRUG PRODUCTS", "OPEN"], "modifyDate": "2021-09-01T18:02:50Z", "dkAbstract": "Docket Status: OPEN", "agencyId": "FDA", "program": "CDER", "shortTitle": "Definition and Option of Alternative Labeling Requirements for Convenience Size OTC Drug Packages", "subType2": null, "title": "Definition and Option of Alternative Labeling Requirements for Convenience Size OTC Drug Packages", "generic": "N", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "1998N-0337C", "subType": null, "category": null, "field2": "OPEN", "effectiveDate": null, "objectId": "0b00006480558e3e"} | single_get |
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