Regulation of Tobacco Products; Extension of Comment Period, 50810 [E9-23607]

Download as PDF 50810 Federal Register / Vol. 74, No. 189 / Thursday, October 1, 2009 / Notices expansion supplement to the National Association for State Community Services Programs (NASCSP), located in Washington, DC, to support performance training and technical assistance on data collection, analysis and dissemination issues faced by state community services programs within the Community Services Block Grant (CSBG) Network; develop performance based reporting tools for ARRA CSBG funded activities; develop and maintain a catalog of innovative programs and practices related to the American Recovery and Reinvestment Act of 2009 (ARRA). The project activities are designed to support and strengthen the ability of the CSBG Network to comply with and carry out CSBG activities funded by ARRA. The training projects and resources developed under the award will include analysis and explanation of the practical impact of ARRA for States and CSBG-eligible entities so that they can work more effectively to reach the ARRA goals and document how they have in fact reached those goals and used the ARRA funds. Contact for Further Information: Danielle Williams, U.S. Department of Health and Human Services, Office of Community Services, Administration for Children and Families, 370 L’Enfant Promenade, SW., Washington, DC 20047, Telephone: (202) 205–4717, Email: Danielle.Williams@acf.hhs.gov. Dated: September 25, 2009. Yolanda J. Butler, Acting Director, Office of Community Services. [FR Doc. E9–23726 Filed 9–30–09; 8:45 am] BILLING CODE P DEPARTMENT OF HEALTH AND HUMAN SERVICES allow interested persons additional time to submit comments. DATES: Submit electronic and written comments by December 28, 2009. Submit electronic comments to https:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA– 305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Erik Mettler, Center for Tobacco Products, Food and Drug Administration, 9200 Corporate Blvd., Rockville, MD, 20850– 3229, 301–796–4830, Erik.Mettler@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background In the Federal Register of July 1, 2009 (74 FR 31457), FDA published a notice with a 90-day comment period to request comments on the implementation of the Tobacco Act. Comments from the public will inform FDA’s actions implementing the Tobacco Act. The agency has received a request for an extension of the comment period for the notice. This request conveyed concern that the current 90-day comment period does not allow sufficient time to develop a meaningful or thoughtful response to the notice. FDA has considered the request and is extending the comment period for the notice for 90 days, until December 28, 2009. The agency believes that a 90-day extension allows adequate time for interested persons to submit comments without significantly delaying rulemaking on these important issues. II. Request for Comments [Docket No. FDA–2009–N–0294] Interested persons may submit to the Division of Dockets Management (see ADDRESSES) electronic or written comments on this document. Submit a single copy of electronic comments or two paper copies of any mailed comments, except that individuals may submit one paper copy. Comments are to be identified with the docket number found in brackets in the heading of this document. Received comments may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. AGENCY: Food and Drug Administration, HHS. PWALKER on DSK8KYBLC1PROD with NOTICES ACTION: Notice; extension of comment period. SUMMARY: The Food and Drug Administration (FDA) is extending to December 28, 2009, the comment period for the notice that appeared in the Federal Register of July 1, 2009 (74 FR 31457). In the notice, FDA requested comments on the implementation of the Family Smoking Prevention and Tobacco Control Act (the Tobacco Act). The agency is taking this action in response to a request for an extension to VerDate Nov<24>2008 19:32 Sep 30, 2009 Jkt 217001 U.S. Citizenship and Immigration Services ADDRESSES: Food and Drug Administration Regulation of Tobacco Products; Extension of Comment Period DEPARTMENT OF HOMELAND SECURITY Dated: September 25, 2009. David Horowitz, Assistant Commissioner for Policy. [FR Doc. E9–23607 Filed 9–28–09; 11:15 am] BILLING CODE 4160–01–S PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 Agency Information Collection Activities: Form N–600; Extension of an Existing Information Collection; Comment Request ACTION: 30-Day Notice of Information Collection Under Review: Form N–600, Application for Certificate of Citizenship; OMB Control Number 1615–0057. The Department of Homeland Security, U.S. Citizenship and Immigration Services (USCIS) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act of 1995. The information collection was previously published in the Federal Register on June 25, 2009, at 74 FR 30315, allowing for a 60-day public comment period. USCIS did not receive any comments. The purpose of this notice is to allow an additional 30 days for public comments. Comments are encouraged and will be accepted until November 2, 2009. This process is conducted in accordance with 5 CFR 1320.10. Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the Department of Homeland Security (DHS), and to the Office of Information and Regulatory Affairs, Office of Management and Budget (OMB), USCIS Desk Officer. Comments may be submitted to: USCIS, Chief, Regulatory Products Division, Clearance Office, 111 Massachusetts Avenue, Washington, DC 20529–2210. Comments may also be submitted to DHS via facsimile to 202– 272–8352 or via e-mail at rfs.regs@dhs.gov, and to the OMB USCIS Desk Officer via facsimile at 202–395– 5806 or via e-mail at oira_submission@omb.eop.gov. When submitting comments by email, please make sure to add OMB Control No. 1615–0057 in the subject box. Written comments and suggestions from the public and affected agencies should address one or more of the following four points: (1) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; E:\FR\FM\01OCN1.SGM 01OCN1

Agencies

[Federal Register Volume 74, Number 189 (Thursday, October 1, 2009)]
[Notices]
[Page 50810]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-23607]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2009-N-0294]


Regulation of Tobacco Products; Extension of Comment Period

AGENCY:  Food and Drug Administration, HHS.

ACTION:  Notice; extension of comment period.

-----------------------------------------------------------------------

SUMMARY:  The Food and Drug Administration (FDA) is extending to 
December 28, 2009, the comment period for the notice that appeared in 
the Federal Register of July 1, 2009 (74 FR 31457). In the notice, FDA 
requested comments on the implementation of the Family Smoking 
Prevention and Tobacco Control Act (the Tobacco Act). The agency is 
taking this action in response to a request for an extension to allow 
interested persons additional time to submit comments.

DATES:  Submit electronic and written comments by December 28, 2009.

ADDRESSES:  Submit electronic comments to https://www.regulations.gov.
    Submit written comments to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, 
Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT:  Erik Mettler, Center for Tobacco 
Products, Food and Drug Administration, 9200 Corporate Blvd., 
Rockville, MD, 20850-3229, 301-796-4830, Erik.Mettler@fda.hhs.gov.

SUPPLEMENTARY INFORMATION:

I. Background

    In the Federal Register of July 1, 2009 (74 FR 31457), FDA 
published a notice with a 90-day comment period to request comments on 
the implementation of the Tobacco Act. Comments from the public will 
inform FDA's actions implementing the Tobacco Act.
    The agency has received a request for an extension of the comment 
period for the notice. This request conveyed concern that the current 
90-day comment period does not allow sufficient time to develop a 
meaningful or thoughtful response to the notice.
    FDA has considered the request and is extending the comment period 
for the notice for 90 days, until December 28, 2009. The agency 
believes that a 90-day extension allows adequate time for interested 
persons to submit comments without significantly delaying rulemaking on 
these important issues.

II. Request for Comments

    Interested persons may submit to the Division of Dockets Management 
(see ADDRESSES) electronic or written comments on this document. Submit 
a single copy of electronic comments or two paper copies of any mailed 
comments, except that individuals may submit one paper copy. Comments 
are to be identified with the docket number found in brackets in the 
heading of this document. Received comments may be seen in the Division 
of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.

    Dated: September 25, 2009.
David Horowitz,
Assistant Commissioner for Policy.
[FR Doc. E9-23607 Filed 9-28-09; 11:15 am]
BILLING CODE 4160-01-S

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.