Agency Information Collection Activities; Submission for OMB Review; Comment Request, 67541-67544 [2020-23515]
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Federal Register / Vol. 85, No. 206 / Friday, October 23, 2020 / Notices
Frequency of Response: On occasion,
annually and semi-annually reporting
requirements; annual recordkeeping
requirement.
Obligation to Respond: Mandatory.
Statutory authority for this information
collection is contained in 47 U.S.C.
154(i), 154(j), 161, 201–205, and 303(r).
Total Annual Burden: 24 hours.
Total Annual Cost: $225,000.
Privacy Act Impact Assessment: No
impact(s).
Nature and Extent of Confidentiality:
Respondents concerned about
disclosure of sensitive information in
any submissions to the Commission
may request confidential treatment
pursuant to 47 CFR 0.459 of the
Commission’s rules.
Needs and Uses: The Commission
will submit this information collection
to the Office of Management and Budget
(OMB) after this 60-day comment period
in order to obtain the full three-year
clearance from them.
The FCC has standards for accounting
authorities in the maritime mobile and
maritime-satellite radio services. The
Commission will use the information to
determine eligibility of applicants for
certification as an accounting authority,
to monitor activity, to ensure
compliance, and to identify accounting
authorities to the International
Telecommunications Union.
Respondents are entities seeking
certification or those already certified to
be accounting authorities.
Federal Communications Commission.
Marlene Dortch,
Secretary, Office of the Secretary.
immediate inspection at the Federal
Reserve Bank(s) indicated below and at
the offices of the Board of Governors.
This information may also be obtained
on an expedited basis, upon request, by
contacting the appropriate Federal
Reserve Bank and from the Board’s
Freedom of Information Office at
https://www.federalreserve.gov/foia/
request.htm. Interested persons may
express their views in writing on the
standards enumerated in the BHC Act
(12 U.S.C. 1842(c)).
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
Street and Constitution Avenue NW,
Washington, DC 20551–0001, not later
than November 23, 2020.
A. Federal Reserve Bank of
Philadelphia (William Spaniel, Senior
Vice President) 100 North 6th Street,
Philadelphia, Pennsylvania 19105–
1521. Comments can also be sent
electronically to
Comments.applications@phil.frb.org:
1. William Penn Bancorporation,
Bristol, Pennsylvania; to become a bank
holding company by acquiring the
voting shares of William Penn Bank,
Bristol, Pennsylvania, in connection
with the merger of William Penn, MHC,
Bristol, Pennsylvania, a state chartered
mutual bank holding company
converting from the mutual to the stock
form, with and into William Penn
Bancorporation.
Board of Governors of the Federal Reserve
System, October 20, 2020.
Yao-Chin Chao,
Assistant Secretary of the Board.
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BILLING CODE 6712–01–P
[FR Doc. 2020–23543 Filed 10–22–20; 8:45 am]
BILLING CODE P
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Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The public portions of the
applications listed below, as well as
other related filings required by the
Board, if any, are available for
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Board, if any, are available for
immediate inspection at the Federal
Reserve Bank(s) indicated below and at
the offices of the Board of Governors.
This information may also be obtained
on an expedited basis, upon request, by
contacting the appropriate Federal
Reserve Bank and from the Board’s
Freedom of Information Office at
https://www.federalreserve.gov/foia/
request.htm. Interested persons may
express their views in writing on the
standards enumerated in the BHC Act
(12 U.S.C. 1842(c)).
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
Street and Constitution Avenue NW,
Washington, DC 20551–0001, not later
than November 23, 2020.
A. Federal Reserve Bank of Chicago
(Colette A. Fried, Assistant Vice
President) 230 South LaSalle Street,
Chicago, Illinois 60690–1414:
1. First Secure Bank Group, Inc.,
Sugar Grove, Illinois, to acquire Wonder
Bancorp, Inc., and thereby indirectly
acquire State Bank, both of Wonder
Lake, Illinois.
Board of Governors of the Federal Reserve
System, October 20, 2020.
Yao-Chin Chao,
Assistant Secretary of the Board.
[FR Doc. 2020–23542 Filed 10–22–20; 8:45 am]
BILLING CODE P
FEDERAL TRADE COMMISSION
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request
Federal Trade Commission
(‘‘FTC’’ or ‘‘Commission’’).
ACTION: Notice.
AGENCY:
FEDERAL RESERVE SYSTEM
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67541
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The public portions of the
applications listed below, as well as
other related filings required by the
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The information collection
requirements described below will be
submitted to the Office of Management
and Budget (‘‘OMB’’) for review, as
required by the Paperwork Reduction
Act (‘‘PRA’’). The FTC seeks public
comments on proposed information
requests sent pursuant to compulsory
process to a combined ten or more of the
largest domestic cigarette manufacturers
and smokeless tobacco manufacturers.
The information sought would include,
among other things, data on annual
sales and marketing expenditures. The
current FTC clearance from the Office of
Management and Budget (‘‘OMB’’) to
conduct such information collection
expires December 31, 2020. The
Commission intends to ask OMB for
SUMMARY:
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Federal Register / Vol. 85, No. 206 / Friday, October 23, 2020 / Notices
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renewed three-year clearance to collect
this information.
DATES: Comments on the proposed
information requests must be received
on or before November 23, 2020.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. The reginfo.gov web
link is a United States Government
website produced by OMB and the
General Services Administration (GSA).
Under PRA requirements, OMB’s Office
of Information and Regulatory Affairs
(OIRA) reviews Federal information
collections.
FOR FURTHER INFORMATION CONTACT:
Requests for additional information or
copies of the proposed collection of
information should be addressed to
Michael Ostheimer, Division of
Advertising Practices, Bureau of
Consumer Protection, Federal Trade
Commission, 600 Pennsylvania Avenue
NW, Mailstop CC–10507, Washington,
DC 20580, (202) 326–2699.
SUPPLEMENTARY INFORMATION:
Title: FTC Cigarette and Smokeless
Tobacco Data Collection.
OMB Control Number: 3084–0134.
Type of Review: Extension of a
currently approved collection.
On June 25, 2020, the FTC sought
public comment on the information
collection requirements associated with
the Cigarette and Smokeless Tobacco
Data Collection. 85 FR 38139. Four
germane comments were received.
Pursuant to the OMB regulations, 5 CFR
part 1320, that implement the PRA, 44
U.S.C. 3501 et seq., the FTC is providing
this second opportunity for public
comment while seeking OMB approval
to renew the pre-existing clearance for
the Cigarette and Smokeless Tobacco
Data Collection.
In response to the June 25, 2020
Notice, the Commission received
comments from the Campaign for
Tobacco-Free Kids (‘‘CTFK’’), the
American Lung Association (‘‘ALA’’),
Truth Initiative, and Altria Client
Services (‘‘Altria’’).
I. CTFK
The CTFK comment specifically
noted the utility and importance of the
Commission’s Cigarette and Smokeless
Tobacco Reports, and urged the agency
to continue collecting and reporting
industry sales and marketing
expenditure data, which CTFK stated
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provide ‘‘critical data to researchers,
policymakers, advocates and the general
public.’’ CTFK additionally observed:
The FTC is currently the only public
source for data on cigarette and smokeless
tobacco companies’ marketing and
promotional expenditures. No other agency
collects and publishes such information
directly from the companies, making the FTC
reports the most accurate and reliable
assessment of tobacco marketing and
promotion expenditures available.
CTFK at 1. CTFK, however, suggested
certain modifications to the
Commission’s reports. Specifically,
CTFK recommended that the
Commission: (1) Clarify in which
category coupons that consumers obtain
online are to be counted; (2) report data
on a company-specific or brand-specific
basis, rather than on a fully-aggregated
basis; (3) require manufacturers to
report expenditures related to corporate
sponsorships and advertisements; and
(4) publish reports within one year of
data collection. Id. at 2. CTFK also
requested that the FTC extend its data
collection to include electronic
cigarettes (‘‘e-cigarettes’’) and cigars.1
The Commission’s proposed Orders
clarify that expenditures on coupons
delivered online should be reported
together with coupons delivered by
other means. The full impact of
couponing by the major cigarette and
smokeless tobacco manufacturers can
only be seen if expenditures for all
coupons are reported together,
regardless of how those coupons are
delivered to consumers.
Regarding CTFK’s suggestion that data
be reported on other than a fullyaggregated, nationwide basis, the
cigarette and smokeless tobacco
companies assert that those data are
confidential and, as CTFK
acknowledges, the Commission cannot
publicly release trade secrets or certain
commercial or financial information. Id.
at 2, n.2.
The Commission has for a number of
years required the recipients of its 6(b)
Orders to report certain expenditures
related to corporate sponsorships and
advertisements made in the name of the
company, rather than any of its brands.2
1 Two other commenters, ALA and Truth
Initiative, made the same suggestion. The collection
of data regarding e-cigarettes or cigars is beyond the
scope of this proposed collection. Note though that
the FTC has a separate ongoing study on ecigarettes. See FTC Press Release, FTC to Study ECigarette Manufacturers’ Sales, Advertising, and
Promotional Methods (Oct. 3, 2019), https://
www.ftc.gov/news-events/press-releases/2019/10/
ftc-study-e-cigarette-manufacturers-salesadvertising-promotional.
2 Both the cigarette and smokeless tobacco Orders
required the recipients to report expenditures on
‘‘public entertainment events (including, but not
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The Commission has not included those
data in its Cigarette and Smokeless
Tobacco Reports, and has therefore
decided to cease collecting this
information.
Regarding CTFK’s suggestion to
publish reports within one year of data
collection, the Commission always
strives to publish the Cigarette and
Smokeless Tobacco Reports as quickly
as possible. It takes the recipients of its
6(b) Orders time to submit their reports
and they may request extensions, such
as this year due to the COVID–19
pandemic. After reviewing the resulting
reports, staff often has to go back to one
or more of the 6(b) Order recipients for
clarifications and corrections. The data
also requires analysis, and the reports
require writing and review and approval
at multiple levels. The Commission
does in fact usually publish the
Cigarette and Smokeless Tobacco
Reports well within a year of when the
data is first submitted.
II. ALA
The ALA comment stated that the
Commission’s Cigarette and Smokeless
Tobacco Reports provide ‘‘valuable
information on cigarette and smokeless
tobacco products sales and marketing
that is used on an ongoing basis in the
Lung Association’s education and
public policy activities related to
preventing and reducing tobacco use.’’
ALA at 1. ALA additionally observed:
These data are also important for public
health officials and other organizations
working to reduce the terrible burden caused
by tobacco. By understanding how much
tobacco companies spend on marketing and
the distribution channels they use, it allows
public health officials to determine where
and how best to deliver tobacco prevention
and cessation messages.
Id.
III. Truth Initiative
Truth Initiative’s comment stressed
the critical importance and utility of the
Cigarette and Smokeless Tobacco
reports. Truth Initiative at 1. It said that
the reports provide information that is
not available elsewhere and is not
duplicative of other data collections. Id.
Truth Initiative believes the reports
often provide the basis for strong public
health policies with regard to tobacco
use and marketing and such policies
save lives. Id.
Truth Initiative, however, suggested
certain modifications to the
limited to, concerts and sporting events) bearing or
otherwise displaying the name of the Company or
any variation thereof but not bearing or otherwise
displaying the name, logo, or an image of any
portion of the package’’ of any of its cigarettes or
smokeless tobacco products, or otherwise referring
to those products.
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Commission’s reports. Specifically,
Truth Initiative recommended that the
Commission: (1) Collect information
regarding heated tobacco products with
its cigarette Orders; (2) collect
information regarding low nicotine
cigarettes; (3) reinstate previously asked
questions requesting lists of new and
discontinued cigarette products; (4)
collect information regarding nicotine
pouches and lozenges that do not
contain tobacco; (5) collect information
regarding the flavors of smokeless
tobacco products; (6) clarify that
streaming shows are included in
questions about product placement; (7)
define ‘‘youth’’ as persons younger than
18 years of age and ‘‘underage’’ as
persons younger than 21 years of age. Id.
at 2–6.
The Commission agrees that heated,
non-combusted tobacco products are an
important emerging segment of the
tobacco market. The Commission plans
to monitor these products and will
consider whether and how best to
collect information about these products
when the market has further developed
to make such information collection
warranted.
As for Truth Initiative’s suggestion
that the Commission collect information
regarding low-nicotine cigarette
products, none of the current recipients
of the cigarette Orders sell such
products. The Commission’s Cigarette
Reports focus on the largest cigarette
manufacturers and do not attempt to
present a complete picture of the
cigarette market. There are numerous
smaller manufacturers and importers of
cigarettes to which the Commission
does not direct its cigarette Orders. The
Commission does not intend, at this
time, to seek information specifically
regarding low nicotine cigarettes or to
direct an Order to the one company that
has expressed an intention in marketing
such products.
In 2017, the Commission determined
that it no longer needed lists of
cigarettes first sold or discontinued in a
calendar year and it does not see a
sufficient basis to revisit that decision.
As the Truth Initiative notes, nicotine
pouches and lozenges are currently
being marketed by some of the major
smokeless tobacco companies, and are
an important emerging segment of the
tobacco market. Id. at 4. The
Commission will add a question to its
smokeless tobacco Orders about total
unit and dollar sales of these products
to help the agency assess whether
collection of more complete information
about such products would be
warranted.
Given the information presented by
the Truth Initiative regarding the
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popularity of flavored smokeless
tobacco, especially among youth (id. at
4), and the Commission’s collection of
flavor information regarding cigarettes
(and recently e-cigarettes), the
Commission will modify its smokeless
tobacco 6(b) Orders to seek information
regarding the flavors of smokeless
tobacco products.
The Commission believes that its
product placement questions that ask
about ‘‘motion picture(s)’’ and
‘‘television show(s)’’ cover ‘‘original
shows streamed via the internet.’’ On
the other hand, the Commission sees no
harm in clarifying that is the case and
intends to do so.
The Truth Initiative correctly points
out that the federal minimum age to
purchase tobacco is now 21. Id. at 6.
The Commission will use the term
‘‘underage persons’’ in lieu of ‘‘youth’’
in its 6(b) Orders and define ‘‘underage
persons’’ as persons younger than 21
years of age.
IV. Altria
Altria stated that the Commission
should no longer collect any
information from cigarette and
smokeless tobacco manufacturers ‘‘due
to the Food and Drug Administration’s
. . . extensive, active regulatory
authority over tobacco products under
the Family Smoking Prevention and
Tobacco Control Act.’’ Altria at 1.
Because FDA has the authority to
require tobacco product manufacturers
to submit additional information to
promulgate additional regulations
regarding advertising and promotion of
tobacco products, Altria calls the
Commission’s collections ‘‘superfluous’’
and unnecessary ‘‘burdens.’’ Id. at 2.
Altria also contends that ‘‘responding to
FTC’s collection requests requires
several full-time employees (across
multiple departments and operating
companies) to spend weeks compiling
data, revising reports, and reviewing
ledgers before preparing for submission
to FTC’’ and that this effort takes ‘‘far
longer than 180 hours’’ estimated by the
Commission as the ‘‘average annual
burden on manufacturers.’’ Id. at 2.
The FTC staff and FDA staff have a
long tradition of working together on the
many areas where the two agencies
share jurisdiction. However, since the
FDA is not collecting cigarette or
smokeless tobacco sales and marketing
expenditure data like that required by
the Commission’s 6(b) Orders, there is
no overlap or duplication with respect
to such data. The Commission intends
to continue collecting cigarette and
smokeless tobacco sales and marketing
expenditure data. To the extent that in
the future FDA duplicates the FTC’s
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67543
data collection, the FTC can modify or
cease its collection.
Altria contends that the Commission
underestimates its burden in responding
to the FTC’s information collection and
that its burden is ‘‘far longer than 180
hours.’’ The Commission’s burden
estimate of 180 hours was an average for
the nine largest recipients of the
Commission’s information request. The
recipients vary greatly in size, in the
number of products that they sell, and
in the extent and variety of their
advertising and promotion. Our burden
estimate clearly stated that the very
largest recipients might require
hundreds of hours. Altria, which owns
Philip Morris USA and the U.S.
Smokeless Tobacco Co., says on its
website that its ‘‘tobacco companies
. . . have been the undisputed market
leaders in the U.S. tobacco industry for
decades.’’ 3 Altria’s comment is
consistent with the number of hours
that its Philip Morris subsidiary
previously told FTC staff that it spent
complying with the Commission’s
cigarette Order. All the other tobacco
companies that responded to the FTC
staff’s latest inquiries reported spending
substantially fewer hours. We also note
that Altria is the recipient of two 6(b)
Orders, one for cigarettes and one for
smokeless tobacco. To err on the side of
caution, the Commission will increase
its burden estimate from 1,980 hours to
2,940 hours.
Burden Statement
Estimated Annual Burden: 2,940
hours.4
Estimated Number of Respondents: 15
6(b) recipients (maximum).5
3 See www.altria.com/aboutaltria?src=megaspotlight.
4 The Commission intends to use this PRA
clearance renewal to collect information from the
companies concerning their marketing and sales
activities for the years 2021, 2022, and 2023. The
Commission expects to issue compulsory process
orders seeking this information annually, but it is
possible that orders might not be issued in any
given year and that orders seeking information for
two years would be issued the next year. The
figures set forth in this notice for the estimated
hours and labor costs associated with this
information collection represent average annual
burden over the course of the prospective PRA
clearance.
5 Since three and possibly more of these 6(b)
recipients are parent companies that have
separately incorporated subsidiaries or affiliates
that the FTC anticipates or expects that the parent
companies will transmit the collection instrument
to and seek information from, the proposal to send
up to 15 6(b) Orders could equate to 20 ‘‘persons’’
under the PRA. See 5 CFR 1320.3(c)(4) (‘‘[ten or
more persons] . . . refers to the persons to whom
a collection of information is addressed by the
agency within any 12-month period, and to any
independent entities to which the initial addressee
may reasonably be expected to transmit the
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These estimates include any time
spent by separately incorporated
subsidiaries and other entities affiliated
with the ultimate parent companies that
receive the information requests.
Estimated Average Burden per Year
Per Request: 196 hours.
(a) Information requests to the four
largest recipients 6 of the Commission’s
information request, at a per request
average each year of 400 hours = 2,400
hours, cumulatively, per year; and
(b) Information requests to nine
additional respondents, of smaller size,
at a per request average each year of 60
hours = 540 hours, cumulatively, per
year.
Estimated Annual Labor Cost:
$294,000.
Estimated Capital or Other Non-Labor
Cost: de minimis.
Request for Comment
Your comment—including your name
and your state—will be placed on the
public record of this proceeding.
Because your comment will be made
public, you are solely responsible for
making sure that your comment does
not include any sensitive personal
information, such as anyone’s Social
Security number; date of birth; driver’s
license number or other state
identification number, or foreign
country equivalent; passport number;
financial account number; or credit or
debit card number. You are also solely
responsible for making sure that your
comment does not include any sensitive
health information, such as medical
records or other individually
identifiable health information. In
addition, your comment should not
include any ‘‘trade secret or any
commercial or financial information
which . . . is privileged or
confidential’’—as provided by Section
6(f) of the FTC Act, 15 U.S.C. 46(f), and
FTC Rule 4.10(a)(2), 16 CFR 4.10(a)(2)—
including in particular competitively
sensitive information such as costs,
sales statistics, inventories, formulas,
patterns, devices, manufacturing
processes, or customer names.
Josephine Liu,
Assistant General Counsel for Legal Counsel.
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BILLING CODE 6750–01–P
collection of information during that period,
including . . . separately incorporated subsidiaries
or affiliates.’’).
6 There are two tobacco companies that receive
both a cigarette Order and a smokeless tobacco
Order. Thus, this would equate to six requests for
burden analysis.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–21–0728; Docket No. CDC–2020–
0096]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled National Notifiable Diseases
Surveillance System—Revision—Center
for Surveillance, Epidemiology and
Laboratory Services (CSELS), Centers for
Disease Control and Prevention (CDC).
The purpose of this data collection is to
provide the official source of statistics
in the United States for nationally
notifiable conditions. Data will be used
to monitor the occurrence and spread of
nationally notifiable conditions. Data
will be gathered through electronic
submissions of case notifications to CDC
from public health departments from 50
states, New York City, Washington DC,
five U.S. territories, and three freely
associated states.
DATES: CDC must receive written
comments on or before December 22,
2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0096 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
SUMMARY:
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To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7118; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
FOR FURTHER INFORMATION CONTACT:
Proposed Project
National Notifiable Diseases
Surveillance System (OMB Control No.
0920–0728, Exp. 04/30/2023)—
Revision—Center for Surveillance,
Epidemiology and Laboratory Services
(CSELS), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Public Health Services Act (42
U.S.C. 241) authorizes CDC to
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Agencies
[Federal Register Volume 85, Number 206 (Friday, October 23, 2020)]
[Notices]
[Pages 67541-67544]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-23515]
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FEDERAL TRADE COMMISSION
Agency Information Collection Activities; Submission for OMB
Review; Comment Request
AGENCY: Federal Trade Commission (``FTC'' or ``Commission'').
ACTION: Notice.
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SUMMARY: The information collection requirements described below will
be submitted to the Office of Management and Budget (``OMB'') for
review, as required by the Paperwork Reduction Act (``PRA''). The FTC
seeks public comments on proposed information requests sent pursuant to
compulsory process to a combined ten or more of the largest domestic
cigarette manufacturers and smokeless tobacco manufacturers. The
information sought would include, among other things, data on annual
sales and marketing expenditures. The current FTC clearance from the
Office of Management and Budget (``OMB'') to conduct such information
collection expires December 31, 2020. The Commission intends to ask OMB
for
[[Page 67542]]
renewed three-year clearance to collect this information.
DATES: Comments on the proposed information requests must be received
on or before November 23, 2020.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. The
reginfo.gov web link is a United States Government website produced by
OMB and the General Services Administration (GSA). Under PRA
requirements, OMB's Office of Information and Regulatory Affairs (OIRA)
reviews Federal information collections.
FOR FURTHER INFORMATION CONTACT: Requests for additional information or
copies of the proposed collection of information should be addressed to
Michael Ostheimer, Division of Advertising Practices, Bureau of
Consumer Protection, Federal Trade Commission, 600 Pennsylvania Avenue
NW, Mailstop CC-10507, Washington, DC 20580, (202) 326-2699.
SUPPLEMENTARY INFORMATION:
Title: FTC Cigarette and Smokeless Tobacco Data Collection.
OMB Control Number: 3084-0134.
Type of Review: Extension of a currently approved collection.
On June 25, 2020, the FTC sought public comment on the information
collection requirements associated with the Cigarette and Smokeless
Tobacco Data Collection. 85 FR 38139. Four germane comments were
received. Pursuant to the OMB regulations, 5 CFR part 1320, that
implement the PRA, 44 U.S.C. 3501 et seq., the FTC is providing this
second opportunity for public comment while seeking OMB approval to
renew the pre-existing clearance for the Cigarette and Smokeless
Tobacco Data Collection.
In response to the June 25, 2020 Notice, the Commission received
comments from the Campaign for Tobacco-Free Kids (``CTFK''), the
American Lung Association (``ALA''), Truth Initiative, and Altria
Client Services (``Altria'').
I. CTFK
The CTFK comment specifically noted the utility and importance of
the Commission's Cigarette and Smokeless Tobacco Reports, and urged the
agency to continue collecting and reporting industry sales and
marketing expenditure data, which CTFK stated provide ``critical data
to researchers, policymakers, advocates and the general public.'' CTFK
additionally observed:
The FTC is currently the only public source for data on
cigarette and smokeless tobacco companies' marketing and promotional
expenditures. No other agency collects and publishes such
information directly from the companies, making the FTC reports the
most accurate and reliable assessment of tobacco marketing and
promotion expenditures available.
CTFK at 1. CTFK, however, suggested certain modifications to the
Commission's reports. Specifically, CTFK recommended that the
Commission: (1) Clarify in which category coupons that consumers obtain
online are to be counted; (2) report data on a company-specific or
brand-specific basis, rather than on a fully-aggregated basis; (3)
require manufacturers to report expenditures related to corporate
sponsorships and advertisements; and (4) publish reports within one
year of data collection. Id. at 2. CTFK also requested that the FTC
extend its data collection to include electronic cigarettes (``e-
cigarettes'') and cigars.\1\
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\1\ Two other commenters, ALA and Truth Initiative, made the
same suggestion. The collection of data regarding e-cigarettes or
cigars is beyond the scope of this proposed collection. Note though
that the FTC has a separate ongoing study on e-cigarettes. See FTC
Press Release, FTC to Study E-Cigarette Manufacturers' Sales,
Advertising, and Promotional Methods (Oct. 3, 2019), https://www.ftc.gov/news-events/press-releases/2019/10/ftc-study-e-cigarette-manufacturers-sales-advertising-promotional.
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The Commission's proposed Orders clarify that expenditures on
coupons delivered online should be reported together with coupons
delivered by other means. The full impact of couponing by the major
cigarette and smokeless tobacco manufacturers can only be seen if
expenditures for all coupons are reported together, regardless of how
those coupons are delivered to consumers.
Regarding CTFK's suggestion that data be reported on other than a
fully-aggregated, nationwide basis, the cigarette and smokeless tobacco
companies assert that those data are confidential and, as CTFK
acknowledges, the Commission cannot publicly release trade secrets or
certain commercial or financial information. Id. at 2, n.2.
The Commission has for a number of years required the recipients of
its 6(b) Orders to report certain expenditures related to corporate
sponsorships and advertisements made in the name of the company, rather
than any of its brands.\2\ The Commission has not included those data
in its Cigarette and Smokeless Tobacco Reports, and has therefore
decided to cease collecting this information.
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\2\ Both the cigarette and smokeless tobacco Orders required the
recipients to report expenditures on ``public entertainment events
(including, but not limited to, concerts and sporting events)
bearing or otherwise displaying the name of the Company or any
variation thereof but not bearing or otherwise displaying the name,
logo, or an image of any portion of the package'' of any of its
cigarettes or smokeless tobacco products, or otherwise referring to
those products.
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Regarding CTFK's suggestion to publish reports within one year of
data collection, the Commission always strives to publish the Cigarette
and Smokeless Tobacco Reports as quickly as possible. It takes the
recipients of its 6(b) Orders time to submit their reports and they may
request extensions, such as this year due to the COVID-19 pandemic.
After reviewing the resulting reports, staff often has to go back to
one or more of the 6(b) Order recipients for clarifications and
corrections. The data also requires analysis, and the reports require
writing and review and approval at multiple levels. The Commission does
in fact usually publish the Cigarette and Smokeless Tobacco Reports
well within a year of when the data is first submitted.
II. ALA
The ALA comment stated that the Commission's Cigarette and
Smokeless Tobacco Reports provide ``valuable information on cigarette
and smokeless tobacco products sales and marketing that is used on an
ongoing basis in the Lung Association's education and public policy
activities related to preventing and reducing tobacco use.'' ALA at 1.
ALA additionally observed:
These data are also important for public health officials and
other organizations working to reduce the terrible burden caused by
tobacco. By understanding how much tobacco companies spend on
marketing and the distribution channels they use, it allows public
health officials to determine where and how best to deliver tobacco
prevention and cessation messages.
Id.
III. Truth Initiative
Truth Initiative's comment stressed the critical importance and
utility of the Cigarette and Smokeless Tobacco reports. Truth
Initiative at 1. It said that the reports provide information that is
not available elsewhere and is not duplicative of other data
collections. Id. Truth Initiative believes the reports often provide
the basis for strong public health policies with regard to tobacco use
and marketing and such policies save lives. Id.
Truth Initiative, however, suggested certain modifications to the
[[Page 67543]]
Commission's reports. Specifically, Truth Initiative recommended that
the Commission: (1) Collect information regarding heated tobacco
products with its cigarette Orders; (2) collect information regarding
low nicotine cigarettes; (3) reinstate previously asked questions
requesting lists of new and discontinued cigarette products; (4)
collect information regarding nicotine pouches and lozenges that do not
contain tobacco; (5) collect information regarding the flavors of
smokeless tobacco products; (6) clarify that streaming shows are
included in questions about product placement; (7) define ``youth'' as
persons younger than 18 years of age and ``underage'' as persons
younger than 21 years of age. Id. at 2-6.
The Commission agrees that heated, non-combusted tobacco products
are an important emerging segment of the tobacco market. The Commission
plans to monitor these products and will consider whether and how best
to collect information about these products when the market has further
developed to make such information collection warranted.
As for Truth Initiative's suggestion that the Commission collect
information regarding low-nicotine cigarette products, none of the
current recipients of the cigarette Orders sell such products. The
Commission's Cigarette Reports focus on the largest cigarette
manufacturers and do not attempt to present a complete picture of the
cigarette market. There are numerous smaller manufacturers and
importers of cigarettes to which the Commission does not direct its
cigarette Orders. The Commission does not intend, at this time, to seek
information specifically regarding low nicotine cigarettes or to direct
an Order to the one company that has expressed an intention in
marketing such products.
In 2017, the Commission determined that it no longer needed lists
of cigarettes first sold or discontinued in a calendar year and it does
not see a sufficient basis to revisit that decision.
As the Truth Initiative notes, nicotine pouches and lozenges are
currently being marketed by some of the major smokeless tobacco
companies, and are an important emerging segment of the tobacco market.
Id. at 4. The Commission will add a question to its smokeless tobacco
Orders about total unit and dollar sales of these products to help the
agency assess whether collection of more complete information about
such products would be warranted.
Given the information presented by the Truth Initiative regarding
the popularity of flavored smokeless tobacco, especially among youth
(id. at 4), and the Commission's collection of flavor information
regarding cigarettes (and recently e-cigarettes), the Commission will
modify its smokeless tobacco 6(b) Orders to seek information regarding
the flavors of smokeless tobacco products.
The Commission believes that its product placement questions that
ask about ``motion picture(s)'' and ``television show(s)'' cover
``original shows streamed via the internet.'' On the other hand, the
Commission sees no harm in clarifying that is the case and intends to
do so.
The Truth Initiative correctly points out that the federal minimum
age to purchase tobacco is now 21. Id. at 6. The Commission will use
the term ``underage persons'' in lieu of ``youth'' in its 6(b) Orders
and define ``underage persons'' as persons younger than 21 years of
age.
IV. Altria
Altria stated that the Commission should no longer collect any
information from cigarette and smokeless tobacco manufacturers ``due to
the Food and Drug Administration's . . . extensive, active regulatory
authority over tobacco products under the Family Smoking Prevention and
Tobacco Control Act.'' Altria at 1. Because FDA has the authority to
require tobacco product manufacturers to submit additional information
to promulgate additional regulations regarding advertising and
promotion of tobacco products, Altria calls the Commission's
collections ``superfluous'' and unnecessary ``burdens.'' Id. at 2.
Altria also contends that ``responding to FTC's collection requests
requires several full-time employees (across multiple departments and
operating companies) to spend weeks compiling data, revising reports,
and reviewing ledgers before preparing for submission to FTC'' and that
this effort takes ``far longer than 180 hours'' estimated by the
Commission as the ``average annual burden on manufacturers.'' Id. at 2.
The FTC staff and FDA staff have a long tradition of working
together on the many areas where the two agencies share jurisdiction.
However, since the FDA is not collecting cigarette or smokeless tobacco
sales and marketing expenditure data like that required by the
Commission's 6(b) Orders, there is no overlap or duplication with
respect to such data. The Commission intends to continue collecting
cigarette and smokeless tobacco sales and marketing expenditure data.
To the extent that in the future FDA duplicates the FTC's data
collection, the FTC can modify or cease its collection.
Altria contends that the Commission underestimates its burden in
responding to the FTC's information collection and that its burden is
``far longer than 180 hours.'' The Commission's burden estimate of 180
hours was an average for the nine largest recipients of the
Commission's information request. The recipients vary greatly in size,
in the number of products that they sell, and in the extent and variety
of their advertising and promotion. Our burden estimate clearly stated
that the very largest recipients might require hundreds of hours.
Altria, which owns Philip Morris USA and the U.S. Smokeless Tobacco
Co., says on its website that its ``tobacco companies . . . have been
the undisputed market leaders in the U.S. tobacco industry for
decades.'' \3\ Altria's comment is consistent with the number of hours
that its Philip Morris subsidiary previously told FTC staff that it
spent complying with the Commission's cigarette Order. All the other
tobacco companies that responded to the FTC staff's latest inquiries
reported spending substantially fewer hours. We also note that Altria
is the recipient of two 6(b) Orders, one for cigarettes and one for
smokeless tobacco. To err on the side of caution, the Commission will
increase its burden estimate from 1,980 hours to 2,940 hours.
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\3\ See www.altria.com/about-altria?src=megaspotlight.
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Burden Statement
Estimated Annual Burden: 2,940 hours.\4\
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\4\ The Commission intends to use this PRA clearance renewal to
collect information from the companies concerning their marketing
and sales activities for the years 2021, 2022, and 2023. The
Commission expects to issue compulsory process orders seeking this
information annually, but it is possible that orders might not be
issued in any given year and that orders seeking information for two
years would be issued the next year. The figures set forth in this
notice for the estimated hours and labor costs associated with this
information collection represent average annual burden over the
course of the prospective PRA clearance.
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Estimated Number of Respondents: 15 6(b) recipients (maximum).\5\
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\5\ Since three and possibly more of these 6(b) recipients are
parent companies that have separately incorporated subsidiaries or
affiliates that the FTC anticipates or expects that the parent
companies will transmit the collection instrument to and seek
information from, the proposal to send up to 15 6(b) Orders could
equate to 20 ``persons'' under the PRA. See 5 CFR 1320.3(c)(4)
(``[ten or more persons] . . . refers to the persons to whom a
collection of information is addressed by the agency within any 12-
month period, and to any independent entities to which the initial
addressee may reasonably be expected to transmit the collection of
information during that period, including . . . separately
incorporated subsidiaries or affiliates.'').
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[[Page 67544]]
These estimates include any time spent by separately incorporated
subsidiaries and other entities affiliated with the ultimate parent
companies that receive the information requests.
Estimated Average Burden per Year Per Request: 196 hours.
(a) Information requests to the four largest recipients \6\ of the
Commission's information request, at a per request average each year of
400 hours = 2,400 hours, cumulatively, per year; and
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\6\ There are two tobacco companies that receive both a
cigarette Order and a smokeless tobacco Order. Thus, this would
equate to six requests for burden analysis.
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(b) Information requests to nine additional respondents, of smaller
size, at a per request average each year of 60 hours = 540 hours,
cumulatively, per year.
Estimated Annual Labor Cost: $294,000.
Estimated Capital or Other Non-Labor Cost: de minimis.
Request for Comment
Your comment--including your name and your state--will be placed on
the public record of this proceeding. Because your comment will be made
public, you are solely responsible for making sure that your comment
does not include any sensitive personal information, such as anyone's
Social Security number; date of birth; driver's license number or other
state identification number, or foreign country equivalent; passport
number; financial account number; or credit or debit card number. You
are also solely responsible for making sure that your comment does not
include any sensitive health information, such as medical records or
other individually identifiable health information. In addition, your
comment should not include any ``trade secret or any commercial or
financial information which . . . is privileged or confidential''--as
provided by Section 6(f) of the FTC Act, 15 U.S.C. 46(f), and FTC Rule
4.10(a)(2), 16 CFR 4.10(a)(2)--including in particular competitively
sensitive information such as costs, sales statistics, inventories,
formulas, patterns, devices, manufacturing processes, or customer
names.
Josephine Liu,
Assistant General Counsel for Legal Counsel.
[FR Doc. 2020-23515 Filed 10-22-20; 8:45 am]
BILLING CODE 6750-01-P