82_FR_10899 82 FR 10868 - Use of the Term “Healthy” in the Labeling of Human Food Products; Public Meeting; Request for Comments

82 FR 10868 - Use of the Term “Healthy” in the Labeling of Human Food Products; Public Meeting; Request for Comments

DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration

Federal Register Volume 82, Issue 31 (February 16, 2017)

Page Range10868-10870
FR Document2017-03117

The Food and Drug Administration (FDA or we) is announcing the following public meeting entitled ``Use of the Term `Healthy' in the Labeling of Human Food Products.'' The purpose of the public meeting is to give interested persons an opportunity to discuss the use of the term ``healthy'' in the labeling of human food.

Federal Register, Volume 82 Issue 31 (Thursday, February 16, 2017)
[Federal Register Volume 82, Number 31 (Thursday, February 16, 2017)]
[Proposed Rules]
[Pages 10868-10870]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2017-03117]


========================================================================
Proposed Rules
                                                Federal Register
________________________________________________________________________

This section of the FEDERAL REGISTER contains notices to the public of 
the proposed issuance of rules and regulations. The purpose of these 
notices is to give interested persons an opportunity to participate in 
the rule making prior to the adoption of the final rules.

========================================================================


Federal Register / Vol. 82, No. 31 / Thursday, February 16, 2017 / 
Proposed Rules

[[Page 10868]]



DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 101

[Docket No. FDA-2016-D-2335]


Use of the Term ``Healthy'' in the Labeling of Human Food 
Products; Public Meeting; Request for Comments

AGENCY: Food and Drug Administration, HHS.

ACTION: Notification of public meeting; request for comments.

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

SUMMARY: The Food and Drug Administration (FDA or we) is announcing the 
following public meeting entitled ``Use of the Term `Healthy' in the 
Labeling of Human Food Products.'' The purpose of the public meeting is 
to give interested persons an opportunity to discuss the use of the 
term ``healthy'' in the labeling of human food.

DATES: The public meeting will be held on March 9, 2017, from 8:30 a.m. 
until 5:30 p.m. See section III ``How to Participate in the Public 
Meeting'' in the SUPPLEMENTARY INFORMATION section of this document for 
dates and times of the public meetings, closing dates for advance 
registration, requesting special accommodations due to disability, and 
other information regarding meeting participation.

ADDRESSES: The public meeting will be held at the Hilton Washington DC/
Rockville Hotel, 1750 Rockville Pike, Rockville, MD 20852.
    You may submit comments as follows:

Electronic Submissions

    Submit electronic comments in the following way:
     Federal eRulemaking Portal: https://www.regulations.gov. 
Follow the instructions for submitting comments. Comments submitted 
electronically, including attachments, to https://www.regulations.gov 
will be posted to the docket unchanged. Because your comment will be 
made public, you are solely responsible for ensuring that your comment 
does not include any confidential information that you or a third party 
may not wish to be posted, such as medical information, your or anyone 
else's Social Security number, or confidential business information, 
such as a manufacturing process. Please note that if you include your 
name, contact information, or other information that identifies you in 
the body of your comments, that information will be posted on https://www.regulations.gov.
     If you want to submit a comment with confidential 
information that you do not wish to be made available to the public, 
submit the comment as a written/paper submission and in the manner 
detailed (see ``Written/Paper Submissions'' and ``Instructions'').

Written/Paper Submissions

    Submit written/paper submissions as follows:
     Mail/Hand delivery/Courier (for written/paper 
submissions): Division of Dockets Management (HFA-305), Food and Drug 
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
     For written/paper comments submitted to the Division of 
Dockets Management, FDA will post your comment, as well as any 
attachments, except for information submitted, marked and identified, 
as confidential, if submitted as detailed in ``Instructions.''
    Instructions: All submissions received must include the Docket No. 
FDA-2016-D-2335 for ``Use of the Term `Healthy' in the Labeling of 
Human Food Products; Request for Information and Comments.'' Received 
comments will be placed in the docket and, except for those submitted 
as ``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Division of Dockets Management between 9 
a.m. and 4 p.m., Monday through Friday.
     Confidential Submissions--To submit a comment with 
confidential information that you do not wish to be made publicly 
available, submit your comments only as a written/paper submission. You 
should submit two copies total. One copy will include the information 
you claim to be confidential with a heading or cover note that states 
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' We will review 
this copy, including the claimed confidential information, in our 
consideration of comments. The second copy, which will have the claimed 
confidential information redacted/blacked out, will be available for 
public viewing and posted on https://www.regulations.gov. Submit both 
copies to the Division of Dockets Management. If you do not wish your 
name and contact information to be made publicly available, you can 
provide this information on the cover sheet and not in the body of your 
comments and you must identify this information as ``confidential.'' 
Any information marked as ``confidential'' will not be disclosed except 
in accordance with 21 CFR 10.20 and other applicable disclosure law. 
For more information about FDA's posting of comments to public dockets, 
see 80 FR 56469, September 18, 2015, or access the information at: 
http://www.fda.gov/regulatoryinformation/dockets/default.htm.
    Docket: For access to the docket to read background documents or 
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in 
the heading of this document, into the ``Search'' box and follow the 
prompts and/or go to the Division of Dockets Management, 5630 Fishers 
Lane, Rm. 1061, Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: 
    For questions about registering for the meeting or to register by 
phone: Jim Nakayama, The Nakamoto Group, Inc., 11820 Parklawn Dr., 
Suite 240, Rockville, MD 20852, 301-468-6535, ext. 212, FAX: 301-468-
6536, email: events@nakamotogroup.com.
    For general questions about the meeting or for special 
accommodations due to a disability: Juanita Yates, Center for Food 
Safety and Applied Nutrition (HFS-009), Food and Drug Administration, 
5001 Campus Dr., College Park, MD 20740, 240-402-1731, email: 
Juanita.yates@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: 

I. Background

    In the Federal Register of September 28, 2016, we published a 
document inviting public comment on the possibility of redefining the 
``healthy'' nutrient content claim for food labeling (81 FR 66562). 
This action was

[[Page 10869]]

consistent with our recently released 2016-2025 Foods and Veterinary 
Medicine (FVM) Program's strategic plan with specific goals for 
nutrition and other planned and recent activity including the issuance 
of final rules updating certain of our nutrition labeling regulations. 
The document also contained several specific questions on which we 
sought input (81 FR 66562 at 66564 to 66565). In the Federal Register 
of December 30, 2016, we published a document extending the comment 
period for the docket to receive information and comments on the use of 
the term ``healthy'' in the labeling of human food (81 FR 96404); the 
comment period, which was originally scheduled to end on January 26, 
2017, was extended to April 26, 2017.
    We also recently announced the availability of a guidance for 
industry entitled ``Use of the Term `Healthy' in the Labeling of Human 
Food Products: Guidance to Industry'' (81 FR 66527). The guidance 
advises manufacturers who wish to use the implied nutrient content 
claim ``healthy'' to label their food products as provided by our 
regulations. More specifically, the guidance advises food manufacturers 
of FDA's intent to exercise enforcement discretion with respect to the 
implied nutrient content claim ``healthy'' on foods that have a fat 
profile of predominantly mono and polyunsaturated fats, but do not meet 
the regulatory definition of ``low fat,'' or that contain at least 10 
percent of the Daily Value (DV) per reference amount customarily 
consumed (RACC) of potassium or vitamin D.
    In addition, we received a citizen petition asking that we update, 
among other things, our nutrient content claim regulations to be 
consistent with current federal dietary guidance (see Docket No. FDA-
2015-P-4564 (citizen petition from KIND LLC)). In particular, the 
petitioners requested that FDA amend the regulation defining the 
nutrient content claim ``healthy'' with respect to total fat intake and 
amend the regulation to emphasize whole foods and dietary patterns 
rather than specific nutrients.

II. Purpose and Format of the Public Meeting

    We are holding the public meeting to give interested parties an 
opportunity to discuss the use of the term ``healthy'' in the labeling 
of human food. At the meeting, following introductory presentations, 
parties will have an opportunity to participate in their choice of 
breakout sessions on topics referenced in the notice and related 
documents and engage in an open comment and question and answer 
session. We invite interested parties to provide information, share 
experiences, and raise issues specifically related to the nutrient 
content claim ``healthy,'' including (but not limited to): ``healthy'' 
as a nutrient-based claim, food component-based claim, or both; 
``healthy'' single definition or definition by category; consumer 
understanding of and responses to the term ``healthy''; and when, if 
ever, the use of the term ``healthy'' may be false or misleading. 
Interested parties may also submit electronic or written comments to 
the docket by April 26, 2017. The agenda and other documents will be 
accessible on our FDA public meetings Web site at http://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm before the 
public meeting.
    In general, the meeting format will include introductory 
presentations, perspectives panels, and multiple opportunities for 
individuals to express their opinions at the meeting through oral 
presentations, participation in breakout sessions, and submission of 
electronic or written comments (see ADDRESSES for information on 
submitting comments). There will be an opportunity for parties who are 
unable to participate in person to join the meeting via Webcast. (See 
section III for more information on the Webcast option.)

III. How To Participate in the Public Meeting

    Due to limited space and time, we encourage all persons who wish to 
attend the meeting to register in advance. There is no fee to register 
for the public meeting, and registration will be on a first-come, 
first-served basis. Early registration is recommended because seating 
is limited. Onsite registration will be accepted, if space permits, 
after all preregistered attendees are seated.
    Those requesting an opportunity to make an oral presentation during 
the time allotted for public comment at the meeting should submit a 
request in advance (see table 1 for details) and provide the specific 
topic or issue to be addressed. Due to the anticipated high level of 
interest in presenting public comment and the limited time available, 
we are allocating 3 minutes to each speaker to make an oral 
presentation. Speakers will be limited to making oral remarks; there 
will not be an opportunity to display materials such as slide shows, 
videos, or other media during the meeting. If time permits, individuals 
or organizations that did not register in advance may be granted the 
opportunity to make an oral presentation. We would like to maximize the 
number of individuals who make a presentation at the meeting and will 
do our best to accommodate all persons who wish to make a presentation 
or express their opinions at the meeting.
    We encourage persons and groups who have similar interests to 
consolidate their information for presentation by a single 
representative. After reviewing the presentation requests, we will 
notify each participant before the meeting of the approximate time 
their presentation is scheduled to begin, and remind them of the 
presentation format (i.e., 3-minute oral presentation without visual 
media).
    Table 1 of this document provides information on participation in 
the public meeting.

          Table 1--Information on Participation in the Meeting and on Submitting Comments to the Docket
----------------------------------------------------------------------------------------------------------------
            Activity                    Date         Electronic addresses        Address       Other information
----------------------------------------------------------------------------------------------------------------
Attend public meeting..........  March 9, 2017,      Preregister at http:/ ..................  Registration
                                  from 8:30 a.m. to   /www.fda.gov/Food/                        check-in begins
                                  5:30 p.m.           NewsEvents/                               at 8 a.m.
                                                      WorkshopsMeetingsCo
                                                      nferences/
                                                      default.htm.
View Webcast...................  March 9, 2017,      Webcast participants  ..................  The Webcast will
                                  from 8:30 a.m. to   are asked to                              have closed
                                  5:30 p.m.           preregister at                            captioning.
                                                      http://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm.

[[Page 10870]]

 
Advance registration...........  Register by March   To participate in     We encourage the    There is no
                                  2, 2017.            person preregister    use of electronic   registration fee
                                                      at http://            registration, if    for the public
                                                      www.fda.gov/Food/     possible \1\.       meeting.
                                                      NewsEvents/
                                                      WorkshopsMeetingsCo
                                                      nferences/
                                                      default.htm.
Request to make an oral          By February 21,     To request to make
 presentation.                    2017.               an oral
                                                      presentation sign-
                                                      up at http://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm.
Submit either electronic or      Submit comments by  http://               Division of         See ADDRESSES for
 written comments.                April 26, 2017.     www.regulations.gov.  Dockets             information on
                                                                            Management (HFA-    submitting
                                                                            305), Food and      comments.
                                                                            Drug
                                                                            Administration,
                                                                            5630 Fishers
                                                                            Lane, Rm. 1061,
                                                                            Rockville, MD
                                                                            20852.
Request special accommodations   Request by          Juanita Yates,        See FOR FURTHER
 due to a disability.             February 21, 2017.  email:                INFORMATION
                                                      Juanita.yates@fda.h   CONTACT.
                                                      hs.gov.
----------------------------------------------------------------------------------------------------------------
\1\ You may also register via email, mail, or fax. Please include your name, title, firm name, address, and
  phone and fax numbers in your registration information and send to: Jim Nakayama (see FOR FURTHER INFORMATION
  CONTACT).

IV. Transcripts and Recorded Video

    Please be advised that as soon as a transcript of the public 
meeting is available, it will be accessible at https://www.regulations.gov. The transcript will also be accessible at the 
Division of Dockets Management (see ADDRESSES) and FDA public meetings 
Web site at http://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm.
    Additionally, we will be video recording the public meeting. Once 
the recorded video is available, it will be accessible on our FDA 
public meetings Web site at http://www.fda.gov/Food/NewsEvents/WorkshopsMeetingsConferences/default.htm.

    Dated: February 10, 2017.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2017-03117 Filed 2-15-17; 8:45 am]
BILLING CODE 4164-01-P



                                                10868

                                                Proposed Rules                                                                                                Federal Register
                                                                                                                                                              Vol. 82, No. 31

                                                                                                                                                              Thursday, February 16, 2017



                                                This section of the FEDERAL REGISTER                    the docket unchanged. Because your                    will review this copy, including the
                                                contains notices to the public of the proposed          comment will be made public, you are                  claimed confidential information, in our
                                                issuance of rules and regulations. The                  solely responsible for ensuring that your             consideration of comments. The second
                                                purpose of these notices is to give interested          comment does not include any                          copy, which will have the claimed
                                                persons an opportunity to participate in the            confidential information that you or a                confidential information redacted/
                                                rule making prior to the adoption of the final
                                                                                                        third party may not wish to be posted,                blacked out, will be available for public
                                                rules.
                                                                                                        such as medical information, your or                  viewing and posted on https://
                                                                                                        anyone else’s Social Security number, or              www.regulations.gov. Submit both
                                                DEPARTMENT OF HEALTH AND                                confidential business information, such               copies to the Division of Dockets
                                                HUMAN SERVICES                                          as a manufacturing process. Please note               Management. If you do not wish your
                                                                                                        that if you include your name, contact                name and contact information to be
                                                Food and Drug Administration                            information, or other information that                made publicly available, you can
                                                                                                        identifies you in the body of your                    provide this information on the cover
                                                21 CFR Part 101                                         comments, that information will be                    sheet and not in the body of your
                                                                                                        posted on https://www.regulations.gov.                comments and you must identify this
                                                [Docket No. FDA–2016–D–2335]                              • If you want to submit a comment                   information as ‘‘confidential.’’ Any
                                                                                                        with confidential information that you                information marked as ‘‘confidential’’
                                                Use of the Term ‘‘Healthy’’ in the
                                                                                                        do not wish to be made available to the               will not be disclosed except in
                                                Labeling of Human Food Products;
                                                                                                        public, submit the comment as a                       accordance with 21 CFR 10.20 and other
                                                Public Meeting; Request for Comments
                                                                                                        written/paper submission and in the                   applicable disclosure law. For more
                                                AGENCY:    Food and Drug Administration,                manner detailed (see ‘‘Written/Paper                  information about FDA’s posting of
                                                HHS.                                                    Submissions’’ and ‘‘Instructions’’).                  comments to public dockets, see 80 FR
                                                ACTION: Notification of public meeting;                 Written/Paper Submissions                             56469, September 18, 2015, or access
                                                request for comments.                                                                                         the information at: http://www.fda.gov/
                                                                                                           Submit written/paper submissions as
                                                                                                                                                              regulatoryinformation/dockets/
                                                SUMMARY:   The Food and Drug                            follows:
                                                                                                           • Mail/Hand delivery/Courier (for                  default.htm.
                                                Administration (FDA or we) is                                                                                    Docket: For access to the docket to
                                                announcing the following public                         written/paper submissions): Division of
                                                                                                                                                              read background documents or the
                                                meeting entitled ‘‘Use of the Term                      Dockets Management (HFA–305), Food
                                                                                                                                                              electronic and written/paper comments
                                                ‘Healthy’ in the Labeling of Human                      and Drug Administration, 5630 Fishers
                                                                                                        Lane, Rm. 1061, Rockville, MD 20852.                  received, go to https://
                                                Food Products.’’ The purpose of the                                                                           www.regulations.gov and insert the
                                                public meeting is to give interested                       • For written/paper comments
                                                                                                        submitted to the Division of Dockets                  docket number, found in brackets in the
                                                persons an opportunity to discuss the                                                                         heading of this document, into the
                                                use of the term ‘‘healthy’’ in the labeling             Management, FDA will post your
                                                                                                        comment, as well as any attachments,                  ‘‘Search’’ box and follow the prompts
                                                of human food.                                                                                                and/or go to the Division of Dockets
                                                                                                        except for information submitted,
                                                DATES: The public meeting will be held                                                                        Management, 5630 Fishers Lane, Rm.
                                                                                                        marked and identified, as confidential,
                                                on March 9, 2017, from 8:30 a.m. until                  if submitted as detailed in                           1061, Rockville, MD 20852.
                                                5:30 p.m. See section III ‘‘How to                      ‘‘Instructions.’’                                     FOR FURTHER INFORMATION CONTACT:
                                                Participate in the Public Meeting’’ in the                 Instructions: All submissions received                For questions about registering for the
                                                SUPPLEMENTARY INFORMATION section of                    must include the Docket No. FDA–                      meeting or to register by phone: Jim
                                                this document for dates and times of the                2016–D–2335 for ‘‘Use of the Term                     Nakayama, The Nakamoto Group, Inc.,
                                                public meetings, closing dates for                      ‘Healthy’ in the Labeling of Human                    11820 Parklawn Dr., Suite 240,
                                                advance registration, requesting special                Food Products; Request for Information                Rockville, MD 20852, 301–468–6535,
                                                accommodations due to disability, and                   and Comments.’’ Received comments                     ext. 212, FAX: 301–468–6536, email:
                                                other information regarding meeting                     will be placed in the docket and, except              events@nakamotogroup.com.
                                                participation.                                          for those submitted as ‘‘Confidential                    For general questions about the
                                                ADDRESSES:   The public meeting will be                 Submissions,’’ publicly viewable at                   meeting or for special accommodations
                                                held at the Hilton Washington DC/                       https://www.regulations.gov or at the                 due to a disability: Juanita Yates, Center
                                                Rockville Hotel, 1750 Rockville Pike,                   Division of Dockets Management                        for Food Safety and Applied Nutrition
                                                Rockville, MD 20852.                                    between 9 a.m. and 4 p.m., Monday                     (HFS–009), Food and Drug
                                                  You may submit comments as                            through Friday.                                       Administration, 5001 Campus Dr.,
                                                follows:                                                   • Confidential Submissions—To                      College Park, MD 20740, 240–402–1731,
                                                                                                        submit a comment with confidential                    email: Juanita.yates@fda.hhs.gov.
                                                Electronic Submissions                                  information that you do not wish to be                SUPPLEMENTARY INFORMATION:
                                                  Submit electronic comments in the                     made publicly available, submit your
jstallworth on DSK7TPTVN1PROD with RULES




                                                following way:                                          comments only as a written/paper                      I. Background
                                                  • Federal eRulemaking Portal:                         submission. You should submit two                        In the Federal Register of September
                                                https://www.regulations.gov. Follow the                 copies total. One copy will include the               28, 2016, we published a document
                                                instructions for submitting comments.                   information you claim to be confidential              inviting public comment on the
                                                Comments submitted electronically,                      with a heading or cover note that states              possibility of redefining the ‘‘healthy’’
                                                including attachments, to https://                      ‘‘THIS DOCUMENT CONTAINS                              nutrient content claim for food labeling
                                                www.regulations.gov will be posted to                   CONFIDENTIAL INFORMATION.’’ We                        (81 FR 66562). This action was


                                           VerDate Sep<11>2014   11:27 Feb 15, 2017   Jkt 241001   PO 00000   Frm 00001   Fmt 4702   Sfmt 4702   E:\FR\FM\16FEP1.SGM   16FEP1


                                                                        Federal Register / Vol. 82, No. 31 / Thursday, February 16, 2017 / Proposed Rules                                                                  10869

                                                consistent with our recently released                     to emphasize whole foods and dietary                        III. How To Participate in the Public
                                                2016–2025 Foods and Veterinary                            patterns rather than specific nutrients.                    Meeting
                                                Medicine (FVM) Program’s strategic                                                                                       Due to limited space and time, we
                                                plan with specific goals for nutrition                    II. Purpose and Format of the Public
                                                                                                          Meeting                                                     encourage all persons who wish to
                                                and other planned and recent activity                                                                                 attend the meeting to register in
                                                including the issuance of final rules                        We are holding the public meeting to                     advance. There is no fee to register for
                                                updating certain of our nutrition                         give interested parties an opportunity to                   the public meeting, and registration will
                                                labeling regulations. The document also                                                                               be on a first-come, first-served basis.
                                                                                                          discuss the use of the term ‘‘healthy’’ in
                                                contained several specific questions on                                                                               Early registration is recommended
                                                                                                          the labeling of human food. At the
                                                which we sought input (81 FR 66562 at                                                                                 because seating is limited. Onsite
                                                                                                          meeting, following introductory
                                                66564 to 66565). In the Federal Register                                                                              registration will be accepted, if space
                                                of December 30, 2016, we published a                      presentations, parties will have an
                                                                                                          opportunity to participate in their                         permits, after all preregistered attendees
                                                document extending the comment                                                                                        are seated.
                                                period for the docket to receive                          choice of breakout sessions on topics
                                                                                                          referenced in the notice and related                           Those requesting an opportunity to
                                                information and comments on the use of                                                                                make an oral presentation during the
                                                the term ‘‘healthy’’ in the labeling of                   documents and engage in an open
                                                                                                          comment and question and answer                             time allotted for public comment at the
                                                human food (81 FR 96404); the                                                                                         meeting should submit a request in
                                                comment period, which was originally                      session. We invite interested parties to
                                                                                                                                                                      advance (see table 1 for details) and
                                                scheduled to end on January 26, 2017,                     provide information, share experiences,
                                                                                                                                                                      provide the specific topic or issue to be
                                                was extended to April 26, 2017.                           and raise issues specifically related to
                                                                                                                                                                      addressed. Due to the anticipated high
                                                   We also recently announced the                         the nutrient content claim ‘‘healthy,’’
                                                                                                                                                                      level of interest in presenting public
                                                availability of a guidance for industry                   including (but not limited to): ‘‘healthy’’                 comment and the limited time available,
                                                entitled ‘‘Use of the Term ‘Healthy’ in                   as a nutrient-based claim, food                             we are allocating 3 minutes to each
                                                the Labeling of Human Food Products:                      component-based claim, or both;                             speaker to make an oral presentation.
                                                Guidance to Industry’’ (81 FR 66527).                     ‘‘healthy’’ single definition or definition                 Speakers will be limited to making oral
                                                The guidance advises manufacturers                        by category; consumer understanding of                      remarks; there will not be an
                                                who wish to use the implied nutrient                      and responses to the term ‘‘healthy’’;                      opportunity to display materials such as
                                                content claim ‘‘healthy’’ to label their                  and when, if ever, the use of the term                      slide shows, videos, or other media
                                                food products as provided by our                          ‘‘healthy’’ may be false or misleading.                     during the meeting. If time permits,
                                                regulations. More specifically, the                       Interested parties may also submit                          individuals or organizations that did not
                                                guidance advises food manufacturers of                    electronic or written comments to the                       register in advance may be granted the
                                                FDA’s intent to exercise enforcement                      docket by April 26, 2017. The agenda                        opportunity to make an oral
                                                discretion with respect to the implied                    and other documents will be accessible                      presentation. We would like to
                                                nutrient content claim ‘‘healthy’’ on                     on our FDA public meetings Web site at                      maximize the number of individuals
                                                foods that have a fat profile of                          http://www.fda.gov/Food/NewsEvents/                         who make a presentation at the meeting
                                                predominantly mono and                                    WorkshopsMeetingsConferences/                               and will do our best to accommodate all
                                                polyunsaturated fats, but do not meet                     default.htm before the public meeting.                      persons who wish to make a
                                                the regulatory definition of ‘‘low fat,’’ or                                                                          presentation or express their opinions at
                                                that contain at least 10 percent of the                      In general, the meeting format will
                                                                                                                                                                      the meeting.
                                                Daily Value (DV) per reference amount                     include introductory presentations,                            We encourage persons and groups
                                                customarily consumed (RACC) of                            perspectives panels, and multiple                           who have similar interests to
                                                potassium or vitamin D.                                   opportunities for individuals to express                    consolidate their information for
                                                   In addition, we received a citizen                     their opinions at the meeting through                       presentation by a single representative.
                                                petition asking that we update, among                     oral presentations, participation in                        After reviewing the presentation
                                                other things, our nutrient content claim                  breakout sessions, and submission of                        requests, we will notify each participant
                                                regulations to be consistent with current                 electronic or written comments (see                         before the meeting of the approximate
                                                federal dietary guidance (see Docket No.                  ADDRESSES for information on                                time their presentation is scheduled to
                                                FDA–2015–P–4564 (citizen petition                         submitting comments). There will be an                      begin, and remind them of the
                                                from KIND LLC)). In particular, the                       opportunity for parties who are unable                      presentation format (i.e., 3-minute oral
                                                petitioners requested that FDA amend                      to participate in person to join the                        presentation without visual media).
                                                the regulation defining the nutrient                      meeting via Webcast. (See section III for                      Table 1 of this document provides
                                                content claim ‘‘healthy’’ with respect to                 more information on the Webcast                             information on participation in the
                                                total fat intake and amend the regulation                 option.)                                                    public meeting.

                                                        TABLE 1—INFORMATION ON PARTICIPATION IN THE MEETING AND ON SUBMITTING COMMENTS TO THE DOCKET
                                                        Activity                        Date                       Electronic addresses                                  Address                                Other information

                                                Attend public meeting        March 9, 2017, from          Preregister at http://www.fda.gov/           ....................................................   Registration check-in
                                                                              8:30 a.m. to 5:30             Food/NewsEvents/                                                                                    begins at 8 a.m.
                                                                              p.m.                          WorkshopsMeetingsConferences/
                                                                                                            default.htm.
jstallworth on DSK7TPTVN1PROD with RULES




                                                View Webcast ............    March 9, 2017, from          Webcast participants are asked to            ....................................................   The Webcast will
                                                                              8:30 a.m. to 5:30             preregister at http://www.fda.gov/                                                                  have closed cap-
                                                                              p.m.                          Food/NewsEvents/                                                                                    tioning.
                                                                                                            WorkshopsMeetingsConferences/
                                                                                                            default.htm.




                                           VerDate Sep<11>2014     11:27 Feb 15, 2017   Jkt 241001   PO 00000   Frm 00002   Fmt 4702   Sfmt 4702   E:\FR\FM\16FEP1.SGM            16FEP1


                                                10870                   Federal Register / Vol. 82, No. 31 / Thursday, February 16, 2017 / Proposed Rules

                                                      TABLE 1—INFORMATION ON PARTICIPATION IN THE MEETING AND ON SUBMITTING COMMENTS TO THE DOCKET—
                                                                                                  Continued
                                                        Activity                        Date                       Electronic addresses                              Address                     Other information

                                                Advance registration ..      Register by March 2,         To participate in person preregister          We encourage the use of elec-          There is no registra-
                                                                              2017.                          at         http://www.fda.gov/Food/         tronic registration, if possible 1.     tion fee for the
                                                                                                             NewsEvents/                                                                         public meeting.
                                                                                                             WorkshopsMeetingsConferences/
                                                                                                             default.htm.
                                                Request to make an           By February 21, 2017         To request to make an oral presen-
                                                  oral presentation.                                         tation     sign-up      at     http://
                                                                                                             www.fda.gov/Food/NewsEvents/
                                                                                                             WorkshopsMeetingsConferences/
                                                                                                             default.htm.
                                                Submit either elec-          Submit comments by           http://www.regulations.gov ................   Division of Dockets Manage-            See ADDRESSES
                                                  tronic or written            April 26, 2017.                                                            ment (HFA–305), Food and               for information on
                                                  comments.                                                                                               Drug Administration, 5630              submitting com-
                                                                                                                                                          Fishers Lane, Rm. 1061,                ments.
                                                                                                                                                          Rockville, MD 20852.
                                                Request special ac-          Request by February          Juanita Yates, email: Juanita.yates@          See FOR FURTHER INFORMA-
                                                  commodations due             21, 2017.                    fda.hhs.gov.                                  TION CONTACT.
                                                  to a disability.
                                                   1 You may also register via email, mail, or fax. Please include your name, title, firm name, address, and phone and fax numbers in your reg-
                                                istration information and send to: Jim Nakayama (see FOR FURTHER INFORMATION CONTACT).


                                                IV. Transcripts and Recorded Video                        http://www.fda.gov/Food/NewsEvents/                      NewsEvents/
                                                                                                          WorkshopsMeetingsConferences/                            WorkshopsMeetingsConferences/
                                                   Please be advised that as soon as a                    default.htm.                                             default.htm.
                                                transcript of the public meeting is
                                                available, it will be accessible at https://                Additionally, we will be video                           Dated: February 10, 2017.
                                                www.regulations.gov. The transcript                       recording the public meeting. Once the                   Leslie Kux,
                                                will also be accessible at the Division of                recorded video is available, it will be                  Associate Commissioner for Policy.
                                                Dockets Management (see ADDRESSES)                        accessible on our FDA public meetings                    [FR Doc. 2017–03117 Filed 2–15–17; 8:45 am]
                                                and FDA public meetings Web site at                       Web site at http://www.fda.gov/Food/                     BILLING CODE 4164–01–P
jstallworth on DSK7TPTVN1PROD with RULES




                                           VerDate Sep<11>2014     11:27 Feb 15, 2017   Jkt 241001   PO 00000   Frm 00003   Fmt 4702   Sfmt 9990   E:\FR\FM\16FEP1.SGM     16FEP1



Document Created: 2018-02-01 15:02:08
Document Modified: 2018-02-01 15:02:08
CategoryRegulatory Information
CollectionFederal Register
sudoc ClassAE 2.7:
GS 4.107:
AE 2.106:
PublisherOffice of the Federal Register, National Archives and Records Administration
SectionProposed Rules
ActionNotification of public meeting; request for comments.
DatesThe public meeting will be held on March 9, 2017, from 8:30 a.m. until 5:30 p.m. See section III ``How to Participate in the Public Meeting'' in the SUPPLEMENTARY INFORMATION section of this document for dates and times of the public meetings, closing dates for advance registration, requesting special accommodations due to disability, and other information regarding meeting participation.
ContactFor questions about registering for the meeting or to register by phone: Jim Nakayama, The Nakamoto Group, Inc., 11820 Parklawn Dr., Suite 240, Rockville, MD 20852, 301-468-6535, ext. 212, FAX: 301-468- 6536, email: [email protected]
FR Citation82 FR 10868 

2025 Federal Register | Disclaimer | Privacy Policy
USC | CFR | eCFR