Food Labeling; Nutrition Labeling of Standard Menu Items in Restaurants and Similar Retail Food Establishments; Extension of Compliance Date, 39675-39676 [2015-16865]
Download as PDF
Federal Register / Vol. 80, No. 132 / Friday, July 10, 2015 / Rules and Regulations
safety data, go to
productdata.aphis.usda.gov.
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3. Section 112.5 is amended as
follows:
■ a. In the introductory text, by
removing the words ‘‘paragraph (c) of
this section and under the master label
system provided in paragraph (d)’’ and
adding the words ‘‘paragraph (d) of this
section and under the master label
system provided in paragraph (e)’’ in
their place.
■ b. In paragraph (a), by removing the
words ‘‘(https://www.aphis.usda.gov/
animal_health/vet_biologics/vb_
forms.shtml)’’ and adding the words
‘‘(productdata.aphis.usda.gov)’’ in their
place.
■ c. By redesignating paragraphs (b)
through (g) as paragraphs (c) through
(h).
■ d. By adding a new paragraph (b).
■ e. In newly redesignated paragraph
(d)(1), by removing the citation
‘‘§ 112.5(d)’’ and adding the words
‘‘paragraph (e) of this section’’ in its
place.
■ f. In newly redesignated paragraph
(e)(1)(ii), by removing the citation
‘‘§ 112.5(d)(1)(iii)’’ and adding the
words ‘‘paragraph (e)(1)(iii) of this
section’’ in its place.
■ g. In newly redesignated paragraph
(e)(1)(iii), by removing the citation
‘‘§ 112.5(d)(1)(i)’’ and adding the words
‘‘paragraph (e)(1)(i) of this section’’ in
its place.
■ h. In newly redesignated paragraph
(e)(1)(iv), by removing the citation
‘‘§ 112.5(d)(1)(ii)’’ and adding the words
‘‘paragraph (e)(1)(ii) of this section’’ in
its place.
■ i. In newly redesignated paragraph (h),
by removing the citation ‘‘§ 112.5(c)’’
and adding the words ‘‘paragraph (d) of
this section’’ in its place.
The addition reads as follows:
■
§ 112.5
Review and approval of labeling.
mstockstill on DSK4VPTVN1PROD with RULES
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(b) A data summary, available on the
Internet at productdata.aphis.usda.gov,
shall be used with each submission of
efficacy and safety data in support of a
label claim. Manufacturers will submit
the efficacy and safety data information
with either the efficacy and safety
studies or at the time of label
submission. This information will be
posted at productdata.aphis.usda.gov to
allow public disclosure of product
performance.
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VerDate Sep<11>2014
16:28 Jul 09, 2015
Jkt 235001
Done in Washington, DC, this 6th day of
July 2015.
Kevin Shea,
Administrator, Animal and Plant Health
Inspection Service.
[FR Doc. 2015–16898 Filed 7–9–15; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 11 and 101
[Docket No. FDA–2011–F–0172]
RIN 0910–AG57
Food Labeling; Nutrition Labeling of
Standard Menu Items in Restaurants
and Similar Retail Food
Establishments; Extension of
Compliance Date
AGENCY:
Food and Drug Administration,
HHS.
Final rule; extension of
compliance date.
ACTION:
The Food and Drug
Administration (FDA or we) is
extending the compliance date for the
final rule requiring disclosure of certain
nutrition information for standard menu
items in certain restaurants and retail
food establishments. The final rule
appeared in the Federal Register of
December 1, 2014. We are taking this
action in response to requests for an
extension and for further clarification of
the rule’s requirements.
DATES:
Effective date: This final rule is
effective December 1, 2015.
Compliance date: Covered
establishments must comply with the
rule published December 1, 2014 (79 FR
71156) by December 1, 2016.
FOR FURTHER INFORMATION CONTACT:
Ashley Rulffes, Center for Food Safety
and Applied Nutrition (HFS–820), Food
and Drug Administration, 5100 Paint
Branch Pkwy., College Park, MD 20740,
240–402–2371, email: ashley.rulffes@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Background
In the Federal Register of December 1,
2014 (79 FR 71156), we published a
final rule requiring disclosure of certain
nutrition information for standard menu
items in certain restaurants and retail
food establishments. The final rule
implements provisions of section
403(q)(5)(H) of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C.
343(q)(5)(H)) and:
PO 00000
Frm 00007
Fmt 4700
Sfmt 4700
39675
• Defines terms, including terms that
describe criteria for determining
whether an establishment is subject to
the rule;
• establishes which foods are subject
to the nutrition labeling requirements
and which foods are not subject to these
requirements;
• requires that calories for standard
menu items be declared on menus and
menu boards that list such foods for
sale;
• requires that calories for standard
menu items that are self-service or on
display be declared on signs adjacent to
such foods;
• requires that written nutrition
information for standard menu items be
available to consumers who ask to see
it;
• requires, on menus and menu
boards, a succinct statement concerning
suggested daily caloric intake (succinct
statement), designed to help the public
understand the significance of the
calorie declarations;
• requires, on menus and menu
boards, a statement regarding the
availability of the written nutrition
information (statement of availability);
• establishes requirements for
determination of nutrient content of
standard menu items;
• establishes requirements for
substantiation of nutrient content
determined for standard menu items,
including requirements for records that
a covered establishment must make
available to FDA within a reasonable
period of time upon request; and
• establishes terms and conditions
under which restaurants and similar
retail food establishments not otherwise
subject to the rule could elect to be
subject to the requirements by
registering with FDA.
In the preamble to the final rule (79
FR 71156 at 71239 through 71241), we
stated that the rule would be effective
on December 1, 2015, and also provided
a compliance date of December 1, 2015,
for covered establishments. The final
rule (at 21 CFR 101.11(a)) defines
‘‘covered establishment’’ as a restaurant
or similar retail food establishment that
is a part of a chain with 20 or more
locations doing business under the same
name (regardless of the type of
ownership, e.g., individual franchises)
and offering for sale substantially the
same menu items, as well as a restaurant
or similar retail food establishment that
is voluntarily registered to be covered
under 21 CFR 101.11(d).
II. Extending the Compliance Date
Since we published the final rule in
the Federal Register, we have received
numerous requests asking us to further
E:\FR\FM\10JYR1.SGM
10JYR1
39676
Federal Register / Vol. 80, No. 132 / Friday, July 10, 2015 / Rules and Regulations
mstockstill on DSK4VPTVN1PROD with RULES
interpret portions of the final rule or to
respond to questions asking whether
specific practices would be acceptable
for purposes of complying with the rule.
We issued a document in the Federal
Register (80 FR 13225, March 13, 2015)
announcing the availability of a ‘‘Small
Entity Compliance Guide’’ for the rule,
and are considering what additional
guidance might be helpful.
Since February 2015, we have
received four requests asking us to
extend the compliance date of the final
rule based on concerns that covered
establishments do not have adequate
time to fully implement the
requirements of the rule by the
compliance date. These requests were
submitted by a large retailer and trade
and other associations, and they provide
information regarding steps involved in
implementation of the requirements.
More specifically, the requests describe
steps involved in developing software,
information systems, and other
technologies for providing nutrition
information in ways that better
correspond to how foods are offered for
sale in covered establishments and
allow for more efficient and productspecific nutrition labeling. In addition,
the requests describe steps involved in
training staff, implementing standard
operating procedures, and developing
and installing updated and consistent
menu boards across all locations within
a chain. Most requests sought to extend
the compliance date by 1 year.
In light of these requests, we have
decided to extend the compliance date
for the final rule to December 1, 2016.
The final rule requirements are intended
to ensure that consumers are provided
accurate, clear, and consistent nutrition
information for foods sold in covered
establishments in a direct and accessible
manner to enable consumers to make
informed and healthful dietary choices.
Therefore, allowing adequate time for
covered establishments to fully
implement the final rule’s requirements,
as described in the requests, helps
accomplish the primary objective of the
final rule and is in the public interest.
and safety, and other advantages;
distributive impacts; and equity). FDA
has developed a regulatory impact
analysis that presents the benefits and
costs of this final rule (Ref. 1). The
Agency believes that this final rule is
not a significant regulatory action under
Executive Order 12866.
The Regulatory Flexibility Act
requires Agencies to analyze regulatory
options that would minimize any
significant impact of a rule on small
entities. Because the final rule changes
the compliance date from December 1,
2015, to December 1, 2016, the Agency
certifies that the final rule will not have
a significant economic impact on a
substantial number of small entities.
Section 202(a) of the Unfunded
Mandates Reform Act of 1995 requires
that Agencies prepare a written
statement, which includes an
assessment of anticipated costs and
benefits, before proposing ‘‘any rule that
includes any Federal mandate that may
result in the expenditure by State, local,
and tribal governments, in the aggregate,
or by the private sector, of $100,000,000
or more (adjusted annually for inflation)
in any one year.’’ The current threshold
after adjustment for inflation is $144
million, using the most current (2014)
Implicit Price Deflator for the Gross
Domestic Product. FDA does not expect
this final rule to result in any 1-year
expenditure that would meet or exceed
this amount.
III. Economic Analysis of Impacts
FDA has examined the impacts of the
final rule under Executive Order 12866,
Executive Order 13563, the Regulatory
Flexibility Act (5 U.S.C. 601–612), and
the Unfunded Mandates Reform Act of
1995 (Pub. L. 104–4). Executive Orders
12866 and 13563 direct Agencies to
assess all costs and benefits of available
regulatory alternatives and, when
regulation is necessary, to select
regulatory approaches that maximize
net benefits (including potential
economic, environmental, public health
VI. Reference
The following reference has been
placed on display in the Division of
Dockets Management (see ADDRESSES)
and may be seen by interested persons
between 9 a.m. and 4 p.m., Monday
through Friday, and is available
electronically at https://
www.regulations.gov. (FDA has verified
the Web site address in this reference
section, but we are not responsible for
any subsequent changes to the Web site
after this document publishes in the
Federal Register.)
VerDate Sep<11>2014
16:28 Jul 09, 2015
Jkt 235001
IV. Paperwork Reduction Act
This final rule contains no collection
of information. Therefore, clearance by
the Office of Management and Budget
under the Paperwork Reduction Act of
1995 is not required.
V. Environmental Impact
We have determined under 21 CFR
25.30(k) that this action is of a type that
does not individually or cumulatively
have a significant effect on the human
environment. Therefore, neither an
environmental assessment nor an
environmental impact statement is
required.
PO 00000
Frm 00008
Fmt 4700
Sfmt 4700
1. FDA, ‘‘Food Labeling; Nutrition Labeling
of Standard Menu Items in Restaurants and
Similar Retail Food Establishments;
Extension of Compliance Date,’’ 2015.
Available at: https://www.fda.gov/AboutFDA/
ReportsManualsForms/Reports/
EconomicAnalyses/.
Dated: July 6, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015–16865 Filed 7–9–15; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF THE TREASURY
Office of Foreign Assets Control
31 CFR Part 591
Venezuela Sanctions Regulations
Office of Foreign Assets
Control, Treasury.
ACTION: Final rule.
AGENCY:
The Department of the
Treasury’s Office of Foreign Assets
Control (OFAC) is issuing regulations to
implement the Venezuela Defense of
Human Rights and Civil Society Act of
2014 (Pub. L. 113–278) and Executive
Order 13692 of March 8, 2015
(‘‘Blocking Property and Suspending
Entry of Certain Persons Contributing to
the Situation in Venezuela’’). OFAC
intends to supplement this part 591
with a more comprehensive set of
regulations, which may include
additional interpretive and definitional
guidance and additional general
licenses and statements of licensing
policy.
SUMMARY:
DATES:
Effective: July 10, 2015.
FOR FURTHER INFORMATION CONTACT:
Assistant Director for Licensing, tel.:
202/622–2480, Assistant Director for
Policy, tel.: 202/622–6746, Assistant
Director for Regulatory Affairs, tel.: 202/
622–4855, Assistant Director for
Sanctions Compliance & Evaluation,
tel.: 202/622–2490, OFAC, or Chief
Counsel (Foreign Assets Control), tel.:
202/622–2410, Office of the General
Counsel, Department of the Treasury
(not toll free numbers).
SUPPLEMENTARY INFORMATION:
Electronic and Facsimile Availability
This document and additional
information concerning OFAC are
available from OFAC’s Web site
(www.treasury.gov/ofac). Certain general
information pertaining to OFAC’s
sanctions programs also is available via
facsimile through a 24-hour fax-ondemand service, tel.: 202/622–0077.
E:\FR\FM\10JYR1.SGM
10JYR1
Agencies
[Federal Register Volume 80, Number 132 (Friday, July 10, 2015)]
[Rules and Regulations]
[Pages 39675-39676]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-16865]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 11 and 101
[Docket No. FDA-2011-F-0172]
RIN 0910-AG57
Food Labeling; Nutrition Labeling of Standard Menu Items in
Restaurants and Similar Retail Food Establishments; Extension of
Compliance Date
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; extension of compliance date.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is extending the
compliance date for the final rule requiring disclosure of certain
nutrition information for standard menu items in certain restaurants
and retail food establishments. The final rule appeared in the Federal
Register of December 1, 2014. We are taking this action in response to
requests for an extension and for further clarification of the rule's
requirements.
DATES:
Effective date: This final rule is effective December 1, 2015.
Compliance date: Covered establishments must comply with the rule
published December 1, 2014 (79 FR 71156) by December 1, 2016.
FOR FURTHER INFORMATION CONTACT: Ashley Rulffes, Center for Food Safety
and Applied Nutrition (HFS-820), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740, 240-402-2371, email:
ashley.rulffes@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of December 1, 2014 (79 FR 71156), we
published a final rule requiring disclosure of certain nutrition
information for standard menu items in certain restaurants and retail
food establishments. The final rule implements provisions of section
403(q)(5)(H) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C.
343(q)(5)(H)) and:
Defines terms, including terms that describe criteria for
determining whether an establishment is subject to the rule;
establishes which foods are subject to the nutrition
labeling requirements and which foods are not subject to these
requirements;
requires that calories for standard menu items be declared
on menus and menu boards that list such foods for sale;
requires that calories for standard menu items that are
self-service or on display be declared on signs adjacent to such foods;
requires that written nutrition information for standard
menu items be available to consumers who ask to see it;
requires, on menus and menu boards, a succinct statement
concerning suggested daily caloric intake (succinct statement),
designed to help the public understand the significance of the calorie
declarations;
requires, on menus and menu boards, a statement regarding
the availability of the written nutrition information (statement of
availability);
establishes requirements for determination of nutrient
content of standard menu items;
establishes requirements for substantiation of nutrient
content determined for standard menu items, including requirements for
records that a covered establishment must make available to FDA within
a reasonable period of time upon request; and
establishes terms and conditions under which restaurants
and similar retail food establishments not otherwise subject to the
rule could elect to be subject to the requirements by registering with
FDA.
In the preamble to the final rule (79 FR 71156 at 71239 through
71241), we stated that the rule would be effective on December 1, 2015,
and also provided a compliance date of December 1, 2015, for covered
establishments. The final rule (at 21 CFR 101.11(a)) defines ``covered
establishment'' as a restaurant or similar retail food establishment
that is a part of a chain with 20 or more locations doing business
under the same name (regardless of the type of ownership, e.g.,
individual franchises) and offering for sale substantially the same
menu items, as well as a restaurant or similar retail food
establishment that is voluntarily registered to be covered under 21 CFR
101.11(d).
II. Extending the Compliance Date
Since we published the final rule in the Federal Register, we have
received numerous requests asking us to further
[[Page 39676]]
interpret portions of the final rule or to respond to questions asking
whether specific practices would be acceptable for purposes of
complying with the rule. We issued a document in the Federal Register
(80 FR 13225, March 13, 2015) announcing the availability of a ``Small
Entity Compliance Guide'' for the rule, and are considering what
additional guidance might be helpful.
Since February 2015, we have received four requests asking us to
extend the compliance date of the final rule based on concerns that
covered establishments do not have adequate time to fully implement the
requirements of the rule by the compliance date. These requests were
submitted by a large retailer and trade and other associations, and
they provide information regarding steps involved in implementation of
the requirements. More specifically, the requests describe steps
involved in developing software, information systems, and other
technologies for providing nutrition information in ways that better
correspond to how foods are offered for sale in covered establishments
and allow for more efficient and product-specific nutrition labeling.
In addition, the requests describe steps involved in training staff,
implementing standard operating procedures, and developing and
installing updated and consistent menu boards across all locations
within a chain. Most requests sought to extend the compliance date by 1
year.
In light of these requests, we have decided to extend the
compliance date for the final rule to December 1, 2016. The final rule
requirements are intended to ensure that consumers are provided
accurate, clear, and consistent nutrition information for foods sold in
covered establishments in a direct and accessible manner to enable
consumers to make informed and healthful dietary choices. Therefore,
allowing adequate time for covered establishments to fully implement
the final rule's requirements, as described in the requests, helps
accomplish the primary objective of the final rule and is in the public
interest.
III. Economic Analysis of Impacts
FDA has examined the impacts of the final rule under Executive
Order 12866, Executive Order 13563, the Regulatory Flexibility Act (5
U.S.C. 601-612), and the Unfunded Mandates Reform Act of 1995 (Pub. L.
104-4). Executive Orders 12866 and 13563 direct Agencies to assess all
costs and benefits of available regulatory alternatives and, when
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety, and other advantages; distributive impacts; and
equity). FDA has developed a regulatory impact analysis that presents
the benefits and costs of this final rule (Ref. 1). The Agency believes
that this final rule is not a significant regulatory action under
Executive Order 12866.
The Regulatory Flexibility Act requires Agencies to analyze
regulatory options that would minimize any significant impact of a rule
on small entities. Because the final rule changes the compliance date
from December 1, 2015, to December 1, 2016, the Agency certifies that
the final rule will not have a significant economic impact on a
substantial number of small entities.
Section 202(a) of the Unfunded Mandates Reform Act of 1995 requires
that Agencies prepare a written statement, which includes an assessment
of anticipated costs and benefits, before proposing ``any rule that
includes any Federal mandate that may result in the expenditure by
State, local, and tribal governments, in the aggregate, or by the
private sector, of $100,000,000 or more (adjusted annually for
inflation) in any one year.'' The current threshold after adjustment
for inflation is $144 million, using the most current (2014) Implicit
Price Deflator for the Gross Domestic Product. FDA does not expect this
final rule to result in any 1-year expenditure that would meet or
exceed this amount.
IV. Paperwork Reduction Act
This final rule contains no collection of information. Therefore,
clearance by the Office of Management and Budget under the Paperwork
Reduction Act of 1995 is not required.
V. Environmental Impact
We have determined under 21 CFR 25.30(k) that this action is of a
type that does not individually or cumulatively have a significant
effect on the human environment. Therefore, neither an environmental
assessment nor an environmental impact statement is required.
VI. Reference
The following reference has been placed on display in the Division
of Dockets Management (see ADDRESSES) and may be seen by interested
persons between 9 a.m. and 4 p.m., Monday through Friday, and is
available electronically at https://www.regulations.gov. (FDA has
verified the Web site address in this reference section, but we are not
responsible for any subsequent changes to the Web site after this
document publishes in the Federal Register.)
1. FDA, ``Food Labeling; Nutrition Labeling of Standard Menu
Items in Restaurants and Similar Retail Food Establishments;
Extension of Compliance Date,'' 2015. Available at: https://www.fda.gov/AboutFDA/ReportsManualsForms/Reports/EconomicAnalyses/.
Dated: July 6, 2015.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2015-16865 Filed 7-9-15; 8:45 am]
BILLING CODE 4164-01-P