Request for Comment on Implementation of the Family Smoking Prevention and Tobacco Control Act, 13241-13243 [2010-6086]
Download as PDF
Federal Register / Vol. 75, No. 53 / Friday, March 19, 2010 / Proposed Rules
FAA AD Differences
Note: This AD differs from the MCAI and/
or service information as follows: No
differences.
Other FAA AD Provisions
(g) The following provisions also apply to
this AD:
(1) Alternative Methods of Compliance
(AMOCs): The Manager, Standards Office,
FAA, has the authority to approve AMOCs
for this AD, if requested using the procedures
found in 14 CFR 39.19. Send information to
Attn: Albert Mercado, Aerospace Engineer,
FAA, Small Airplane Directorate, 901 Locust,
Room 301, Kansas City, Missouri 64106;
telephone: (816) 329–4119; fax: (816) 329–
4090. Before using any approved AMOC on
any airplane to which the AMOC applies,
notify your appropriate principal inspector
(PI) in the FAA Flight Standards District
Office (FSDO), or lacking a PI, your local
FSDO.
(2) Airworthy Product: For any requirement
in this AD to obtain corrective actions from
a manufacturer or other source, use these
actions if they are FAA-approved. Corrective
actions are considered FAA-approved if they
are approved by the State of Design Authority
(or their delegated agent). You are required
to assure the product is airworthy before it
is returned to service.
(3) Reporting Requirements: For any
reporting requirement in this AD, under the
provisions of the Paperwork Reduction Act
(44 U.S.C. 3501 et seq.), the Office of
Management and Budget (OMB) has
approved the information collection
requirements and has assigned OMB Control
Number 2120–0056.
Related Information
(h) Refer to MCAI EASA AD No.: 2010–
0012, dated February 5, 2010; DAHER–
SOCATA TBM Aircraft Service Bulletin SB
70–183, dated January 2010; and L’Hotellier
Service Bulletin 863520–26–001, dated
December 21, 2009, for related information.
Issued in Kansas City, Missouri, on March
15, 2010.
James E. Jackson,
Acting Manager, Small Airplane Directorate,
Aircraft Certification Service.
[FR Doc. 2010–6091 Filed 3–18–10; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
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21 CFR Part 1140
[Docket No. FDA–2010–N–0136]
RIN 0910–AG33
Request for Comment on
Implementation of the Family Smoking
Prevention and Tobacco Control Act
AGENCY:
Food and Drug Administration,
HHS.
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ACTION: Advance notice of proposed
rulemaking.
SUMMARY: The Food and Drug
Administration (FDA) is issuing this
advance notice of proposed rulemaking
to obtain information related to the
regulation of outdoor advertising of
cigarettes and smokeless tobacco.
Elsewhere in this issue of the Federal
Register, FDA is reissuing a final rule
restricting the sale, distribution, and use
of cigarettes and smokeless tobacco to
protect children and adolescents as
required by the Family Smoking
Prevention and Tobacco Control Act
(Tobacco Control Act). FDA has
reserved a section of that final rule for
future rulemaking on restrictions related
to the outdoor advertising of cigarettes
and smokeless tobacco. FDA is
requesting comments, data, research, or
other information on the regulation of
outdoor advertising of cigarettes and
smokeless tobacco.
DATES: Submit electronic or written
comments by May 18, 2010.
ADDRESSES: You may submit comments,
identified by Docket No. FDA–2010–N–
0136 and/or RIN number 0910–AG33,
by any of the following methods:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Written Submissions
Submit written submissions in the
following ways:
• FAX: 301–827–6870.
• Mail/Hand delivery/Courier (for
paper, disk, or CD–ROM submissions):
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
Instructions: All submissions received
must include the agency name and
docket number and Regulatory
Information Number (RIN) for this
rulemaking. All comments received may
be posted without change to https://
www.regulations.gov, including any
personal information provided. For
additional information on submitting
comments, see the ‘‘Comments’’ heading
of the SUPPLEMENTARY INFORMATION
section of this document.
Docket: For access to the docket to
read background documents or
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.
PO 00000
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13241
FOR FURTHER INFORMATION CONTACT:
Annette Marthaler, Center for Tobacco
Products, Food and Drug
Administration, 9200 Corporate Blvd.,
Rockville, MD 20850–3229, 1–877–287–
1373, annette.marthaler@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Elsewhere in this issue of the Federal
Register, FDA is reissuing a 1996 final
rule that restricts the sale, distribution,
and use of cigarettes and smokeless
tobacco. The reissuance of the final rule
is required under section 102 of the
Tobacco Control Act (Public Law 111–
31). More specifically, section 102
requires FDA to publish a final rule
regarding cigarettes and smokeless
tobacco identical in its provisions to the
regulation promulgated by FDA in 1996
(61 FR 44396, August 28, 1996) (1996
final rule), with certain specified
exceptions. Section 102 provides that
the reissued 1996 final rule shall
‘‘include such modifications to section
897.30(b), if any, that the Secretary
determines are appropriate in light of
governing First Amendment case law,
including the decision of the Supreme
Court of the United States in Lorillard
Tobacco Co. v. Reilly (533 U.S. 525
(2001)).’’
As published in 1996, § 897.30(b)
stated that ‘‘[n]o outdoor advertising for
cigarettes or smokeless tobacco,
including billboards, posters, or
placards, may be placed within 1,000
feet of the perimeter of any public
playground or playground area in a
public park (e.g., a public park with
equipment such as swings and seesaws,
baseball diamonds, or basketball courts),
elementary school, or secondary
school.’’ In Lorillard the Supreme Court
struck down as violative of the First
Amendment regulations promulgated by
Massachusetts that, among other things,
banned outdoor tobacco advertisements
within 1,000 feet of any school or
playground. The Supreme Court
concluded that Massachusetts had a
substantial state interest in protecting
children and adolescents from the
harms of tobacco use and that the
outdoor advertising restriction advanced
that interest. However, the Court ruled
that the regulation violated the First
Amendment because it was not
adequately tailored to achieve the
substantial state interest of protecting
children and adolescents from tobacco
products.
To best determine what modifications
to § 897.30(b), if any, are appropriate in
light of governing First Amendment
case law, FDA has determined that
§ 897.30(b) (now renumbered as
§ 1140.30(b)) should be reserved in the
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Federal Register / Vol. 75, No. 53 / Friday, March 19, 2010 / Proposed Rules
final rule published elsewhere in this
issue of the Federal Register and that
the agency should request the
submission of any comments, data,
research, or other information
pertaining to potential outdoor
advertising restrictions for tobacco
products that may have developed since
the 1996 issuance of § 897.30(b). This
approach enables the agency to
implement a regulatory approach to
outdoor advertising that reflects careful
consideration of the U.S. Supreme
Court’s decision in Lorillard, other
provisions in the Tobacco Control Act,
and other developments and
information, such as the Master
Settlement Agreement between the State
Attorneys General and the tobacco
industry, that have occurred since the
original publication of the 1996 final
rule. FDA intends to use the information
submitted in response to this document,
along with information in the existing
record and other information developed
since the publication of the 1996 final
rule, to inform its regulation of outdoor
advertising of cigarettes and smokeless
tobacco.
For example, since the publication of
the 1996 rule, the U.S. National Cancer
Institute (NCI) published its 19th
monograph in the Tobacco Control
Monograph Series, The Role of the
Media in Promoting and Reducing
Tobacco Use (Monograph 19).
Monograph 19 is a ‘‘comprehensive
distillation of the scientific literature on
media communications in tobacco
promotion and tobacco control.’’ In
examining tobacco advertising,
Monograph 19 stated that ‘‘tobacco
advertising forms part of an integrated
marketing communications strategy
combining sponsorship, brand
merchandising, brand stretching,
packaging, point-of-sale promotions,
and product placement.’’ The major
conclusions of Monograph 19 included
the following: (1) Cigarettes are among
the most heavily marketed products in
the United States; (2) the targeting of
various population groups, including
youth and young adults, ‘‘has been
strategically important to the tobacco
industry’’; and (3) the weight of the
evidence demonstrates a causal
relationship between tobacco
advertising and promotion and
increased tobacco use. With respect to
marketing of tobacco to children and
adolescents, Monograph 19 concluded,
among other things, that: (1) Tobacco
advertising targets the psychological
needs of adolescents (e.g., popularity)
and ‘‘adolescents who believe that
smoking can satisfy their psychological
needs, or whose desired image of
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14:13 Mar 18, 2010
Jkt 220001
themselves is similar to their image of
smokers, are more likely to smoke
cigarettes’’; and (2) even brief exposure
to tobacco advertising influences
adolescents’ intentions to smoke.
Monograph 19 stated that ‘‘cigarette
advertising and promotion are heavy in
volume and high in visibility at the
point of sale, particularly in
convenience stores.’’ Monograph 19 also
stated ‘‘[i]n 2001, a cross-section of 586
California retailers was found to have
more than 17 tobacco point-of-purchase
ads, on average, in or around the store
* * * 11% had large exterior signs—in
violation of the [Master Settlement
Agreement].’’ In addition, Monograph 19
cited a study involving 3,000 students
in grades 9 to 12 who smoked, which
found ‘‘their cigarette brand preferences
correlated with the brands most heavily
advertised in the convenience stores
within a one-mile radius of their
schools.’’
Monograph 19 contained an extensive
discussion of the colors and symbols
associated with cigarette brands and
found that colors and symbols can be
used in ways that facilitate the
circumvention of tobacco advertising
restrictions. Monograph 19 found that
the ‘‘brand image of most tobacco
products represents the end result of a
multifaceted marketing effort involving
brand identity * * * and the use of
color. The development, enhancement,
and reinforcement of this brand imagery
are primary objectives of tobacco
promotion.’’
II. Restrictions Under Consideration
The agency is considering several
options, including a regulation
proposing to (1) Prohibit or otherwise
limit billboards located within 1,000
feet of any elementary or secondary
school (k-12) and (2) prohibit or
otherwise limit large signs or collections
of advertisements greater than 14 square
feet at retail establishments located in
close proximity to any elementary or
secondary school (e.g., within 350 feet
or approximately one city block). As
required by Lorillard and the governing
First Amendment case law, any
proposed restrictions would be more
narrowly tailored than § 897.30(b), as
published in 1996. The agency is
considering whether the restrictions
under consideration in this advance
notice of proposed rulemaking that
would differentiate between large and
small advertisements would
appropriately tailor the rule. For
example, we are considering tailoring
the distance requirement by leaving the
1,000 foot restriction for the largest and
most prominent advertisements
(billboards) and narrowing the distance
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Fmt 4702
Sfmt 4702
to 350 feet (approximately one city
block) for smaller advertisements that
are not as prominent. Under this
approach, the restrictions would limit
advertising near schools only, rather
than schools and playgrounds.
III. Request for Comments and
Information
FDA is seeking data, research,
information, and comments on whether
restrictions on outdoor advertising of
tobacco products are necessary to
protect children and adolescents from
the harms caused by tobacco use and, if
they are, whether the restrictions under
consideration, or close variations would
be justified, lawful, and appropriate.
FDA is also seeking data, research,
information, and comments on other
restrictions on outdoor advertising that,
either in addition to or instead of the
specific restrictions under
consideration, would advance the
public health goal of protecting children
and adolescents from the harms caused
by tobacco use.
FDA is seeking data, research,
information, and comments related to
the following:
• Would restrictions advance the
public health goal of protecting children
and adolescents from the harms caused
by tobacco use?
• If so, could this public health goal
be achieved with narrower restrictions?
For example,
» by prohibiting billboards located at
some distance less than 1,000 feet of an
elementary or secondary school?
» by prohibiting signs or collections
of advertisements that are larger than
some size greater than 14 square feet at
retail establishments located within 350
feet of an elementary or secondary
school?
» by prohibiting signs or collections
of advertisements greater than 14 square
feet at retail establishments located
within some distance less than within
350 feet of an elementary or secondary
school?
• Or would a broader prohibition be
necessary to achieve the public health
goal? For example,
» by prohibiting other outdoor
advertisements in addition to those
described in section II of this document?
» by prohibiting smaller notices on
store windows?
» by prohibiting advertisements, not
only near schools, but also near
playgrounds (and, if so, how should
‘‘playgrounds’’ be defined)?
• Should FDA consider requiring
stores that sell tobacco products to post
graphic anti-tobacco messages in order
to counter the effects of advertisements
on children?
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Federal Register / Vol. 75, No. 53 / Friday, March 19, 2010 / Proposed Rules
FDA is also seeking data, research,
information, and comments—not
limited to the specific restrictions under
consideration—related to the following:
• The impact and/or effect(s) of
outdoor advertising restrictions on
youth smoking behavior;
• The increased or decreased
likelihood that persons exposed to
outdoor advertising will start using
tobacco products;
• The increased or decreased
likelihood that persons exposed to
outdoor advertising will continue to use
tobacco products or will be less likely
to stop using tobacco products;
• The impact of outdoor advertising
restrictions based upon distance from
schools in major metropolitan areas;
• The impact of outdoor advertising
restrictions based upon distance from
schools in rural, suburban, and urban
areas and how the impact may differ in
such areas;
• The impact of outdoor advertising
restrictions based upon the size, type, or
other characteristic of the
advertisement;
• The impact of warnings included in
promotional materials, including
outdoor advertising;
• The impact of outdoor advertising
restrictions on tobacco manufacturers or
other sellers’ ability to communicate
with adult smokers;
• Restrictions on outdoor advertising
that, either in addition to or instead of
the specific restrictions under
consideration, would advance the
public health goal of protecting children
and adolescents from the harms caused
by tobacco use.
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IV. Comments
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) electronic or written
comments regarding 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: March 11, 2010.
Margaret A. Hamburg,
Commissioner of Food and Drugs.
Dated: March 11, 2010.
Kathleen Sebelius,
Secretary of Health and Human Services.
[FR Doc. 2010–6086 Filed 3–18–10; 8:45 am]
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DEPARTMENT OF HOUSING AND
URBAN DEVELOPMENT
24 CFR Part 1000
[Docket No. FR–5275–N–06]
Native American Housing Assistance
and Self-Determination
Reauthorization Act of 2008:
Negotiated Rulemaking Committee
Meeting
AGENCY: Office of the Assistant
Secretary for Public and Indian
Housing, HUD.
ACTION: Notice of negotiated rulemaking
committee meeting.
SUMMARY: This document announces a
meeting of the negotiated rulemaking
committee that was established
pursuant to the Native American
Housing Assistance and SelfDetermination Reauthorization Act of
2008. The primary purpose of the
committee is to discuss and negotiate a
proposed rule that would change the
regulations for the Indian Housing Block
Grant (IHBG) program and the Title VI
Loan Guarantee program.
DATES: The committee meeting will be
held on Tuesday, March 30, 2010,
Wednesday, March 31, and Thursday,
April 1, 2010. On all three days the
meeting will begin at 8 am and is
scheduled to end at 5 pm.
ADDRESSES: The meeting will take place
at the Doubletree Paradise Valley Resort,
5401 North Scottsdale Road, Scottsdale,
Arizona 85250; telephone number 480–
946–1524 (this is not a toll-free
number).
FOR FURTHER INFORMATION CONTACT:
Rodger J. Boyd, Deputy Assistant
Secretary for Native American
Programs, Office of Public and Indian
Housing, Department of Housing and
Urban Development, 451 Seventh Street,
SW., Room 4126, Washington, DC
20410; telephone number 202–401–7914
(this is not a toll-free number). Hearing
or speech-impaired individuals may
access this number via TTY by calling
the toll-free Federal Information Relay
Service at 1–800–877–8339.
SUPPLEMENTARY INFORMATION:
I. Background
The Native American Housing
Assistance and Self-Determination
Reauthorization Act of 2008 (Pub. L.
110–411, approved October 14, 2008)
(NAHASDA Reauthorization)
reauthorizes The Native American
Housing Assistance and SelfDetermination Act of 1996 (25 U.S.C.
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Sfmt 9990
13243
4101 et seq.) (NAHASDA) through
September 30, 2013, and makes a
number of amendments to the statutory
requirements governing the Indian
Housing Block Grant Program (IHBG)
and Title VI Loan Guarantee programs.
For more information on the IHBG and
Title VI of NAHASDA, please see the
background section of the Notice of
Negotiated Rulemaking Committee
Meeting published on February 22, 2010
at (75 FR 7579). The NAHASDA
Reauthorization amends section 106 of
NAHASDA to provide that HUD shall
initiate a negotiated rulemaking in order
to implement aspects of the 2008
Reauthorization Act that require
rulemaking. On January 5, 2010 (75 FR
423), HUD published a Federal Register
notice announcing the final list of
members of the negotiated rulemaking
committee (the Native American
Housing Assistance & SelfDetermination Negotiated Rulemaking
Committee). On February 22, 2010 (75
FR 7559), HUD published a Federal
Register notice announcing the first
meeting of the negotiated rulemaking
committee.
II. Negotiated Rulemaking Committee
Meeting
This document announces the second
meeting of the Native American
Housing Assistance & SelfDetermination Negotiated Rulemaking
Committee. The committee meeting will
take place as described in the DATES and
ADDRESSES sections of this document.
The agenda planned for the meeting
includes the discussion of protocols and
the scope of the rulemaking process, as
well as setting of future meetings. The
meeting will be open to the public
without advance registration. Public
attendance may be limited to the space
available. Members of the public may be
allowed to make statements during the
meeting, to the extent time permits, and
to file written statements with the
committee for its consideration. Written
statements should be submitted to the
address listed in the FOR FURTHER
INFORMATION CONTACT section of this
document.
Dated: March 12, 2010.
Sandra B. Henriquez,
Assistant Secretary for Public and Indian
Housing.
[FR Doc. 2010–6003 Filed 3–18–10; 8:45 am]
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Agencies
[Federal Register Volume 75, Number 53 (Friday, March 19, 2010)]
[Proposed Rules]
[Pages 13241-13243]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-6086]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 1140
[Docket No. FDA-2010-N-0136]
RIN 0910-AG33
Request for Comment on Implementation of the Family Smoking
Prevention and Tobacco Control Act
AGENCY: Food and Drug Administration, HHS.
ACTION: Advance notice of proposed rulemaking.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is issuing this advance
notice of proposed rulemaking to obtain information related to the
regulation of outdoor advertising of cigarettes and smokeless tobacco.
Elsewhere in this issue of the Federal Register, FDA is reissuing a
final rule restricting the sale, distribution, and use of cigarettes
and smokeless tobacco to protect children and adolescents as required
by the Family Smoking Prevention and Tobacco Control Act (Tobacco
Control Act). FDA has reserved a section of that final rule for future
rulemaking on restrictions related to the outdoor advertising of
cigarettes and smokeless tobacco. FDA is requesting comments, data,
research, or other information on the regulation of outdoor advertising
of cigarettes and smokeless tobacco.
DATES: Submit electronic or written comments by May 18, 2010.
ADDRESSES: You may submit comments, identified by Docket No. FDA-2010-
N-0136 and/or RIN number 0910-AG33, by any of the following methods:
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Written Submissions
Submit written submissions in the following ways:
FAX: 301-827-6870.
Mail/Hand delivery/Courier (for paper, disk, or CD-ROM
submissions): Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Instructions: All submissions received must include the agency name
and docket number and Regulatory Information Number (RIN) for this
rulemaking. All comments received may be posted without change to
https://www.regulations.gov, including any personal information
provided. For additional information on submitting comments, see the
``Comments'' heading of the SUPPLEMENTARY INFORMATION section of this
document.
Docket: For access to the docket to read background documents or
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: Annette Marthaler, Center for Tobacco
Products, Food and Drug Administration, 9200 Corporate Blvd.,
Rockville, MD 20850-3229, 1-877-287-1373,
annette.marthaler@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Elsewhere in this issue of the Federal Register, FDA is reissuing a
1996 final rule that restricts the sale, distribution, and use of
cigarettes and smokeless tobacco. The reissuance of the final rule is
required under section 102 of the Tobacco Control Act (Public Law 111-
31). More specifically, section 102 requires FDA to publish a final
rule regarding cigarettes and smokeless tobacco identical in its
provisions to the regulation promulgated by FDA in 1996 (61 FR 44396,
August 28, 1996) (1996 final rule), with certain specified exceptions.
Section 102 provides that the reissued 1996 final rule shall ``include
such modifications to section 897.30(b), if any, that the Secretary
determines are appropriate in light of governing First Amendment case
law, including the decision of the Supreme Court of the United States
in Lorillard Tobacco Co. v. Reilly (533 U.S. 525 (2001)).''
As published in 1996, Sec. 897.30(b) stated that ``[n]o outdoor
advertising for cigarettes or smokeless tobacco, including billboards,
posters, or placards, may be placed within 1,000 feet of the perimeter
of any public playground or playground area in a public park (e.g., a
public park with equipment such as swings and seesaws, baseball
diamonds, or basketball courts), elementary school, or secondary
school.'' In Lorillard the Supreme Court struck down as violative of
the First Amendment regulations promulgated by Massachusetts that,
among other things, banned outdoor tobacco advertisements within 1,000
feet of any school or playground. The Supreme Court concluded that
Massachusetts had a substantial state interest in protecting children
and adolescents from the harms of tobacco use and that the outdoor
advertising restriction advanced that interest. However, the Court
ruled that the regulation violated the First Amendment because it was
not adequately tailored to achieve the substantial state interest of
protecting children and adolescents from tobacco products.
To best determine what modifications to Sec. 897.30(b), if any,
are appropriate in light of governing First Amendment case law, FDA has
determined that Sec. 897.30(b) (now renumbered as Sec. 1140.30(b))
should be reserved in the
[[Page 13242]]
final rule published elsewhere in this issue of the Federal Register
and that the agency should request the submission of any comments,
data, research, or other information pertaining to potential outdoor
advertising restrictions for tobacco products that may have developed
since the 1996 issuance of Sec. 897.30(b). This approach enables the
agency to implement a regulatory approach to outdoor advertising that
reflects careful consideration of the U.S. Supreme Court's decision in
Lorillard, other provisions in the Tobacco Control Act, and other
developments and information, such as the Master Settlement Agreement
between the State Attorneys General and the tobacco industry, that have
occurred since the original publication of the 1996 final rule. FDA
intends to use the information submitted in response to this document,
along with information in the existing record and other information
developed since the publication of the 1996 final rule, to inform its
regulation of outdoor advertising of cigarettes and smokeless tobacco.
For example, since the publication of the 1996 rule, the U.S.
National Cancer Institute (NCI) published its 19th monograph in the
Tobacco Control Monograph Series, The Role of the Media in Promoting
and Reducing Tobacco Use (Monograph 19). Monograph 19 is a
``comprehensive distillation of the scientific literature on media
communications in tobacco promotion and tobacco control.'' In examining
tobacco advertising, Monograph 19 stated that ``tobacco advertising
forms part of an integrated marketing communications strategy combining
sponsorship, brand merchandising, brand stretching, packaging, point-
of-sale promotions, and product placement.'' The major conclusions of
Monograph 19 included the following: (1) Cigarettes are among the most
heavily marketed products in the United States; (2) the targeting of
various population groups, including youth and young adults, ``has been
strategically important to the tobacco industry''; and (3) the weight
of the evidence demonstrates a causal relationship between tobacco
advertising and promotion and increased tobacco use. With respect to
marketing of tobacco to children and adolescents, Monograph 19
concluded, among other things, that: (1) Tobacco advertising targets
the psychological needs of adolescents (e.g., popularity) and
``adolescents who believe that smoking can satisfy their psychological
needs, or whose desired image of themselves is similar to their image
of smokers, are more likely to smoke cigarettes''; and (2) even brief
exposure to tobacco advertising influences adolescents' intentions to
smoke.
Monograph 19 stated that ``cigarette advertising and promotion are
heavy in volume and high in visibility at the point of sale,
particularly in convenience stores.'' Monograph 19 also stated ``[i]n
2001, a cross-section of 586 California retailers was found to have
more than 17 tobacco point-of-purchase ads, on average, in or around
the store * * * 11% had large exterior signs--in violation of the
[Master Settlement Agreement].'' In addition, Monograph 19 cited a
study involving 3,000 students in grades 9 to 12 who smoked, which
found ``their cigarette brand preferences correlated with the brands
most heavily advertised in the convenience stores within a one-mile
radius of their schools.''
Monograph 19 contained an extensive discussion of the colors and
symbols associated with cigarette brands and found that colors and
symbols can be used in ways that facilitate the circumvention of
tobacco advertising restrictions. Monograph 19 found that the ``brand
image of most tobacco products represents the end result of a
multifaceted marketing effort involving brand identity * * * and the
use of color. The development, enhancement, and reinforcement of this
brand imagery are primary objectives of tobacco promotion.''
II. Restrictions Under Consideration
The agency is considering several options, including a regulation
proposing to (1) Prohibit or otherwise limit billboards located within
1,000 feet of any elementary or secondary school (k-12) and (2)
prohibit or otherwise limit large signs or collections of
advertisements greater than 14 square feet at retail establishments
located in close proximity to any elementary or secondary school (e.g.,
within 350 feet or approximately one city block). As required by
Lorillard and the governing First Amendment case law, any proposed
restrictions would be more narrowly tailored than Sec. 897.30(b), as
published in 1996. The agency is considering whether the restrictions
under consideration in this advance notice of proposed rulemaking that
would differentiate between large and small advertisements would
appropriately tailor the rule. For example, we are considering
tailoring the distance requirement by leaving the 1,000 foot
restriction for the largest and most prominent advertisements
(billboards) and narrowing the distance to 350 feet (approximately one
city block) for smaller advertisements that are not as prominent. Under
this approach, the restrictions would limit advertising near schools
only, rather than schools and playgrounds.
III. Request for Comments and Information
FDA is seeking data, research, information, and comments on whether
restrictions on outdoor advertising of tobacco products are necessary
to protect children and adolescents from the harms caused by tobacco
use and, if they are, whether the restrictions under consideration, or
close variations would be justified, lawful, and appropriate. FDA is
also seeking data, research, information, and comments on other
restrictions on outdoor advertising that, either in addition to or
instead of the specific restrictions under consideration, would advance
the public health goal of protecting children and adolescents from the
harms caused by tobacco use.
FDA is seeking data, research, information, and comments related to
the following:
Would restrictions advance the public health goal of
protecting children and adolescents from the harms caused by tobacco
use?
If so, could this public health goal be achieved with
narrower restrictions? For example,
[ctrcir] by prohibiting billboards located at some distance less
than 1,000 feet of an elementary or secondary school?
[ctrcir] by prohibiting signs or collections of advertisements that
are larger than some size greater than 14 square feet at retail
establishments located within 350 feet of an elementary or secondary
school?
[ctrcir] by prohibiting signs or collections of advertisements
greater than 14 square feet at retail establishments located within
some distance less than within 350 feet of an elementary or secondary
school?
Or would a broader prohibition be necessary to achieve the
public health goal? For example,
[ctrcir] by prohibiting other outdoor advertisements in addition to
those described in section II of this document?
[ctrcir] by prohibiting smaller notices on store windows?
[ctrcir] by prohibiting advertisements, not only near schools, but
also near playgrounds (and, if so, how should ``playgrounds'' be
defined)?
Should FDA consider requiring stores that sell tobacco
products to post graphic anti-tobacco messages in order to counter the
effects of advertisements on children?
[[Page 13243]]
FDA is also seeking data, research, information, and comments--not
limited to the specific restrictions under consideration--related to
the following:
The impact and/or effect(s) of outdoor advertising
restrictions on youth smoking behavior;
The increased or decreased likelihood that persons exposed
to outdoor advertising will start using tobacco products;
The increased or decreased likelihood that persons exposed
to outdoor advertising will continue to use tobacco products or will be
less likely to stop using tobacco products;
The impact of outdoor advertising restrictions based upon
distance from schools in major metropolitan areas;
The impact of outdoor advertising restrictions based upon
distance from schools in rural, suburban, and urban areas and how the
impact may differ in such areas;
The impact of outdoor advertising restrictions based upon
the size, type, or other characteristic of the advertisement;
The impact of warnings included in promotional materials,
including outdoor advertising;
The impact of outdoor advertising restrictions on tobacco
manufacturers or other sellers' ability to communicate with adult
smokers;
Restrictions on outdoor advertising that, either in
addition to or instead of the specific restrictions under
consideration, would advance the public health goal of protecting
children and adolescents from the harms caused by tobacco use.
IV. Comments
Interested persons may submit to the Division of Dockets Management
(see ADDRESSES) electronic or written comments regarding 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: March 11, 2010.
Margaret A. Hamburg,
Commissioner of Food and Drugs.
Dated: March 11, 2010.
Kathleen Sebelius,
Secretary of Health and Human Services.
[FR Doc. 2010-6086 Filed 3-18-10; 8:45 am]
BILLING CODE 4160-01-S