Advisory Committees; Filing of Closed Meeting Reports, 5380 [2011-1992]
Download as PDF
<![CDATA[
5380
Federal Register / Vol. 76, No. 20 / Monday, January 31, 2011 / Notices
Dated: January 25, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–1998 Filed 1–28–11; 8:45 am]
BILLING CODE 4163–18–P
Dated: January 26, 2011.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2011–1992 Filed 1–28–11; 8:45 am]
Food and Drug Administration
BILLING CODE 4160–01–P
[Docket No. FDA 2011–N–0002]
Advisory Committees; Filing of Closed
Meeting Reports
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
The Food and Drug
Administration (FDA) is announcing
that, as required by the Federal
Advisory Committee Act, the Agency
has filed with the Library of Congress
the annual reports of those FDA
advisory committees that held closed
meetings during fiscal year 2010.
ADDRESSES: Copies are available from
the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852, 301–827–
6860.
SUMMARY:
jlentini on DSKJ8SOYB1PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
Teresa L. Hays, Committee Management
Officer, Advisory Committee and
Oversight Management Staff, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 32, rm. 5290,
Silver Spring, MD 20993–0002, 301–
796–8220.
SUPPLEMENTARY INFORMATION: Under
section 10(d) of the Federal Advisory
Committee Act (5 U.S.C. app.1) and 21
CFR 14.60(d), FDA has filed with the
Library of Congress the annual reports
for the following FDA advisory
committees that held closed meetings
during the period October 1, 2009,
through September 30, 2010:
Center for Biologics Evaluation and
Research:
Blood Products Advisory Committee,
Vaccines and Related Biological
Products Advisory Committee.
National Center for Toxicological
Research:
Science Board to the National Center
for Toxicological Research.
Annual reports are available for
public inspections between 9 a.m. and
4 p.m., Monday through Friday at the
following locations:
1. The Library of Congress, Madison
Bldg., Newspaper and Current
16:38 Jan 28, 2011
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0567]
Notice.
VerDate Mar<15>2010
Periodical Reading Room, 101
Independence Ave., SE., rm. 133,
Washington, DC; and
2. The Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
Jkt 223001
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Restaurant Menu
and Vending Machine Labeling:
Recordkeeping and Mandatory Third
Party Disclosure Under Section 4205 of
the Patient Protection and Affordable
Care Act of 2010
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by March 2,
2011.
SUMMARY:
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or e-mailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0665. Also
include the FDA docket number found
in brackets in the heading of this
document.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3793.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
collection of information to OMB for
review and clearance.
Restaurant Menu and Vending Machine
Labeling: Recordkeeping and
Mandatory Third Party Disclosure
Under Section 4205 of the Patient
Protection and Affordable Care Act of
2010—(OMB Control Number 0910–
0665)—Revision
On March 23, 2010, the President
signed into law the Patient Protection
and Affordable Care Act of 2010
(‘‘Affordable Care Act’’) (Pub. L. 111–
148). Section 4205 of the legislation,
which principally amends sections 403
and 403A of the Federal Food, Drug,
and Cosmetic Act (the FD&C Act) (21
U.S.C. 343 and 343–1), requires chain
restaurants and similar retail food
establishments (SRFE) with 20 or more
locations doing business under the same
name and offering for sale substantially
the same menu items (hereinafter ‘‘chain
retail food establishments’’), as well as
operators of 20 or more vending
machines (hereinafter ‘‘chain vending
machine operators’’), to disclose certain
nutrition information for certain food
items offered for sale so that consumers
can make more informed choices about
the food they purchase. Section 4205 of
the Affordable Care Act preempts State
and local governments from establishing
menu labeling requirements for chain
retail food establishments and vending
machine nutrition labeling requirements
that are not ‘‘identical to’’ the section
4205 requirements.
Section 4205 became effective on the
date the law was signed, March 23,
2010. The provisions that went into
immediate effect are as follows:
For chain retail food establishments:
• Disclosing the number of calories in
each standard menu item on menus and
menu boards,
• Making additional written nutrition
information available to consumers
upon request,
• Providing a statement on menus
and menu boards about the availability
of the written nutrition information, and
• Providing calorie information (per
serving or per food item) for self-service
items and food on display, in a sign
adjacent to each food item.
For chain vending machine operators:
• Providing a sign in close proximity
to each article of food (or the selection
button) that discloses the number of
calories contained in the article, unless
a prospective purchaser is able to
examine the Nutrition Facts Panel
before purchasing the article, or visible
nutrition information is otherwise
provided at the point of purchase.
E:\FR\FM\31JAN1.SGM
31JAN1
]]>Agencies
[Federal Register Volume 76, Number 20 (Monday, January 31, 2011)]
[Notices]
[Page 5380]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-1992]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA 2011-N-0002]
Advisory Committees; Filing of Closed Meeting Reports
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that, as
required by the Federal Advisory Committee Act, the Agency has filed
with the Library of Congress the annual reports of those FDA advisory
committees that held closed meetings during fiscal year 2010.
ADDRESSES: Copies are available from the Division of Dockets Management
(HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852, 301-827-6860.
FOR FURTHER INFORMATION CONTACT: Teresa L. Hays, Committee Management
Officer, Advisory Committee and Oversight Management Staff, Food and
Drug Administration, 10903 New Hampshire Ave., Bldg. 32, rm. 5290,
Silver Spring, MD 20993-0002, 301-796-8220.
SUPPLEMENTARY INFORMATION: Under section 10(d) of the Federal Advisory
Committee Act (5 U.S.C. app.1) and 21 CFR 14.60(d), FDA has filed with
the Library of Congress the annual reports for the following FDA
advisory committees that held closed meetings during the period October
1, 2009, through September 30, 2010:
Center for Biologics Evaluation and Research:
Blood Products Advisory Committee,
Vaccines and Related Biological Products Advisory Committee.
National Center for Toxicological Research:
Science Board to the National Center for Toxicological Research.
Annual reports are available for public inspections between 9 a.m.
and 4 p.m., Monday through Friday at the following locations:
1. The Library of Congress, Madison Bldg., Newspaper and Current
Periodical Reading Room, 101 Independence Ave., SE., rm. 133,
Washington, DC; and
2. The Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Dated: January 26, 2011.
Jill Hartzler Warner,
Acting Associate Commissioner for Special Medical Programs.
[FR Doc. 2011-1992 Filed 1-28-11; 8:45 am]
BILLING CODE 4160-01-P
