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HHS/FDA | RIN: 0910-AG59 | Publication ID: 2012 |
Title: Requirements for the Testing and Reporting of Tobacco Product Constituents, Ingredients, and Additives | |
Abstract: The Federal Food, Drug, and Cosmetic Act, as amended by the Family Smoking Prevention and Tobacco Control Act, requires the Food and Drug Administration to promulgate regulations that require the testing and reporting of tobacco product constituents, ingredients, and additives, including smoke constituents, that the agency determines should be tested to protect the public health. | |
Agency: Department of Health and Human Services(HHS) | Priority: Other Significant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Proposed Rule Stage |
Major: Undetermined | Unfunded Mandates: Undetermined |
CFR Citation: Not Yet Determined (To search for a specific CFR, visit the Code of Federal Regulations.) | |
Legal Authority: 21 USC 301 et seq, 21 USC 387, The Family Smoking Prevention and Tobacco Control Act |
Legal Deadline:
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Overall Description of Deadline: Final rule must issue no later than 36 months after April 1, 2010--see section 915(a) of the Federal Food, Drug, and Cosmetic Act and section 6 of the Family Smoking Prevention and Tobacco Control Act. |
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Timetable:
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Regulatory Flexibility Analysis Required: Yes | Government Levels Affected: Undetermined |
Small Entities Affected: Businesses | Federalism: Undetermined |
Included in the Regulatory Plan: No | |
RIN Data Printed in the FR: Yes | |
Agency Contact: Carol Drew Regulatory Counsel Department of Health and Human Services Food and Drug Administration Office of Good Clinical Practice, WO 32, Room 5105, 10903 New Hampshire Avenue, Silver Spring, MD 20993 Phone:301 796-3505 Email: carol.drew@fda.hhs.gov |