federal_register: E6-21019

All Federal Register documents (rules, proposed rules, notices, presidential documents) from 1994 to present. Nearly 1M documents with full-text search.

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
E6-21019 Over-the-Counter Human Drugs; Labeling Requirements; Proposed Rule Proposed Rule The Food and Drug Administration (FDA) is proposing to amend its final rule that established standardized format and content requirements for the labeling of over-the-counter (OTC) drug products (Drug Facts Rule, codified at 21 CFR 201.66). This amendment proposes a definition and the option of alternative labeling requirements for "convenience-size" OTC drug packages. 2006-12-12 2006 12 https://www.federalregister.gov/documents/2006/12/12/E6-21019/over-the-counter-human-drugs-labeling-requirements-proposed-rule https://www.govinfo.gov/content/pkg/FR-2006-12-12/pdf/E6-21019.pdf Health and Human Services Department; Food and Drug Administration 221,199 The Food and Drug Administration (FDA) is proposing to amend its final rule that established standardized format and content requirements for the labeling of over-the-counter (OTC) drug products (Drug Facts Rule, codified at 21 CFR 201.66). This...

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