Petition To Amend Statement of Interpretation and Enforcement Policy Regarding Labeling of Household Products Containing Methylene Chloride; Request for Comments, 60298-60299 [2016-20928]
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60298
Federal Register / Vol. 81, No. 170 / Thursday, September 1, 2016 / Proposed Rules
Privacy Act protections to all
individuals when systems of records
maintain information on U.S. citizens,
lawful permanent residents, and
visitors. DHS is claiming exemptions
from certain requirements of the Privacy
Act for DHS/CBP–022 Electronic Visa
Update System (EVUS) System of
Records. Some information in DHS/
CBP–022 Electronic Visa Update System
(EVUS) System of Records relates to
official DHS national security, law
enforcement, immigration, and
intelligence activities. These
exemptions are needed to protect
information relating to DHS activities
from disclosure to subjects or others
related to these activities. Specifically,
the exemptions are required to preclude
subjects of these activities from
frustrating these processes. Disclosure of
information to the subject of the inquiry
could also permit the subject to avoid
detection or apprehension.
In appropriate circumstances, when
compliance would not appear to
interfere with or adversely affect the law
enforcement purposes of this system
and the overall law enforcement
process, the applicable exemptions may
be waived on a case by case basis.
A notice of system of records for DHS/
CBP–022 Electronic Visa Update System
(EVUS) System of Records is also
published in this issue of the Federal
Register.
List of Subjects in 6 CFR Part 5
Freedom of information; Privacy.
For the reasons stated in the
preamble, DHS proposes to amend
chapter I of title 6, Code of Federal
Regulations, as follows:
PART 5—DISCLOSURE OF RECORDS
AND INFORMATION
1. The authority citation for part 5
continues to read as follows:
■
Authority: Pub. L. 107–296, 116 Stat. 2135;
(6 U.S.C. 101 et seq.); 5 U.S.C. 301. Subpart
A also issued under 5 U.S.C. 552. Subpart B
also issued under 5 U.S.C. 552a.
proceedings there under; and national
security and intelligence activities. The DHS/
CBP–022 Electronic Visa Update System
(EVUS) System of Records contains
information that is collected by, on behalf of,
in support of, or in cooperation with DHS
and its components and may contain
personally identifiable information collected
by other Federal, State, local, tribal, foreign,
or international government agencies. The
Secretary of Homeland Security, pursuant to
5 U.S.C. 552a(j)(2), has exempted this system
from the following provisions of the Privacy
Act: 5 U.S.C. 552a(c)(3), (e)(8), and (g).
Additionally, the Secretary of Homeland
Security, pursuant to 5 U.S.C. 552a(k)(2) has
exempted this system from the following
provisions of the Privacy Act: 5 U.S.C.
552a(c)(3). Exemptions from these particular
subsections are justified, on a case-by-case
basis to be determined at the time a request
is made, for the following reasons:
(a) From subsection (c)(3) (Accounting for
Disclosures) because release of the
accounting of disclosures could alert the
subject of an investigation of an actual or
potential criminal, civil, or regulatory
violation to the existence of that investigation
and reveal investigative interest on the part
of DHS as well as the recipient agency.
Disclosure of the accounting would therefore
present a serious impediment to law
enforcement efforts and/or efforts to preserve
national security. Disclosure of the
accounting would also permit the individual
who is the subject of a record to impede the
investigation, to tamper with witnesses or
evidence, and to avoid detection or
apprehension, which would undermine the
entire investigative process.
(b) From subsection (e)(8) (Notice on
Individuals) because compliance would
interfere with DHS’s ability to obtain, serve,
and issue subpoenas, warrants, and other law
enforcement mechanisms that may be filed
under seal and could result in disclosure of
investigative techniques, procedures, and
evidence.
(c) From subsection (g) (Civil Remedies) to
the extent that the system is exempt from
other specific subsections of the Privacy Act.
Dated: August 29, 2016.
Jonathan R. Cantor,
Acting Chief Privacy Officer, Department of
Homeland Security.
[FR Doc. 2016–21099 Filed 8–31–16; 8:45 am]
BILLING CODE 9111–14–P
2. In appendix C, add paragraph 74 to
read as follows:
■
CONSUMER PRODUCT SAFETY
COMMISSION
*
asabaliauskas on DSK3SPTVN1PROD with PROPOSALS
Appendix C to Part 5—DHS Systems of
Records Exempt From the Privacy Act
16 CFR Chapter II
*
*
*
*
74. The DHS/CBP–022 Electronic Visa
Update System (EVUS) System of Records
consists of electronic and paper records and
will be used by DHS and its components. The
DHS/CBP–022 Electronic Visa Update
System (EVUS) System of Records is a
repository of information held by DHS in
connection with its several and varied
missions and functions, including, but not
limited to the enforcement of civil and
criminal laws; investigations, inquiries, and
VerDate Sep<11>2014
16:57 Aug 31, 2016
Jkt 238001
[Docket No. CPSC–2016–0019]
Petition To Amend Statement of
Interpretation and Enforcement Policy
Regarding Labeling of Household
Products Containing Methylene
Chloride; Request for Comments
Consumer Product Safety
Commission.
AGENCY:
PO 00000
Frm 00002
Fmt 4702
Sfmt 4702
ACTION:
Notice of petition.
The United States Consumer
Product Safety Commission (CPSC or
Commission) received a petition
requesting that the Commission amend
the agency’s 1987 Statement of
Interpretation and Enforcement Policy
regarding labeling of household
products containing methylene chloride
(Policy Statement). The petition asks the
Commission to expand the Policy
Statement to address acute hazards from
inhalation of methylene chloride vapors
in addition to the chronic hazards
addressed by the current Policy
Statement. The Commission invites
written comments concerning the
petition.
DATES: The Office of the Secretary must
receive comments on the petition by
October 31, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CPSC–2016–
0019, by any of the following methods:
Electronic Submissions: Submit
electronic comments to the Federal
eRulemaking Portal at: https://
www.regulations.gov. Follow the
instructions for submitting comments.
The Commission does not accept
comments submitted by electronic mail
(email), except through
www.regulations.gov. The Commission
encourages you to submit electronic
comments by using the Federal
eRulemaking Portal, as described above.
Written Submissions: Submit written
submissions by mail/hand delivery/
courier to: Office of the Secretary,
Consumer Product Safety Commission,
Room 820, 4330 East West Highway,
Bethesda, MD 20814; telephone (301)
504–7923.
Instructions: All submissions received
must include the agency name and
docket number for this proposed
rulemaking. All comments received may
be posted without change, including
any personal identifiers, contact
information, or other personal
information provided, to: https://
www.regulations.gov. Do not submit
confidential business information, trade
secret information, or other sensitive or
protected information that you do not
want to be available to the public. If
furnished at all, such information
should be submitted in writing.
Docket: For access to the docket to
read background documents or
comments received, go to: https://
www.regulations.gov, and insert the
docket number, CPSC–2016–0019, into
the ‘‘Search’’ box, and follow the
prompts. A copy of the petition is
available at https://www.regulations.gov
under Docket No. CPSC–2016–0019,
Supporting and Related Materials.
SUMMARY:
E:\FR\FM\01SEP1.SGM
01SEP1
Federal Register / Vol. 81, No. 170 / Thursday, September 1, 2016 / Proposed Rules
asabaliauskas on DSK3SPTVN1PROD with PROPOSALS
FOR FURTHER INFORMATION CONTACT:
Todd Stevenson, Office of the Secretary,
U.S. Consumer Product Safety
Commission, Room 820, 4330 East West
Highway, Bethesda, MD 20814;
telephone (301) 504–6833.
SUPPLEMENTARY INFORMATION: The
Commission received a petition from
the Halogenated Solvents Industry
Alliance, Inc. (Petitioner) requesting
that the Commission amend the
agency’s Statement of Interpretation and
Enforcement Policy regarding labeling
of household products containing
methylene chloride (Policy Statement).
The Policy Statement provides the
Commission’s guidance for labeling of
household products containing
methylene chloride, focusing
particularly on paint strippers. 52 FR
34698 (Sep. 14, 1987). The Policy
Statement sets forth general principles
and examples for labeling to warn
consumers of potential cancer hazards;
it does not address acute hazards.
The Petitioner asks the Commission to
expand the Policy Statement to address
acute hazards from inhalation of
methylene chloride vapors. Petitioner
notes that the Occupational Safety and
Health Administration (OSHA) and the
National Institute for Occupational
Safety and Health (NIOSH) issued a
Hazard Alert identifying at least 14
deaths associated with use of methylene
chloride-containing paint strippers by
professional bathtub refinishing
operations (https://www.osha.gov/dts/
hazardalerts/methylene_chloride_
hazard_alert.html). Although the
Petitioner refers to incidents involving
workers, as the Commission’s Policy
Statement indicates, methylene chloride
paint strippers are household products
available for consumers to purchase and
use. Petitioner asserts that revising the
Policy Statement to give specific
guidance on labeling for the acute
hazard posed by inhalation of
methylene chloride vapors, particularly
when used in an enclosed space, such
as when refinishing bathtubs, would
help to prevent future fatalities.
By this notice, the Commission seeks
comments concerning this petition.
Interested parties may obtain a copy of
the petition from the Commission’s Web
site: https://www.cpsc.gov/RegulationsLaws--Standards/Rulemaking/Petitions/
or by writing or calling the Office of the
Secretary, U.S. Consumer Product
Safety Commission, Room 820, 4330
East West Highway, Bethesda, MD
20814; telephone (301) 504–7923. A
copy of the petition is also available for
viewing under ‘‘Supporting and Related
Materials’’ in: www.regulations.gov,
under Docket No. CPSC–2016–0019 .
VerDate Sep<11>2014
16:57 Aug 31, 2016
Jkt 238001
Dated: August 2, 2016.
Todd A. Stevenson,
Secretary, U.S. Consumer Product Safety
Commission.
[FR Doc. 2016–20928 Filed 8–31–16; 8:45 am]
BILLING CODE 6355–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 15
[Docket No. FDA–2016–N–1149]
Manufacturer Communications
Regarding Unapproved Uses of
Approved or Cleared Medical
Products; Public Hearing; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
Notification of public hearing;
request for comments.
ACTION:
The Food and Drug
Administration (FDA or Agency) is
announcing a 2-day public hearing to
obtain input on issues related to
communications by manufacturers,
packers, and distributors, including
their representatives (collectively
‘‘firms’’), regarding FDA-regulated drugs
and medical devices for humans,
including those that are licensed as
biological products, and animal drugs
(collectively, ‘‘medical products’’). FDA
is engaged in a comprehensive review of
its regulations and policies governing
firms’ communications about
unapproved uses of approved/cleared
medical products, and the input from
this meeting will inform FDA’s policy
development in this area. FDA is
seeking input on a number of specific
questions, but is interested in any other
pertinent information participants
would like to share.
DATES: The public hearing will be held
on November 9 and 10, 2016, from 9
a.m. to 5 p.m. The meeting may be
extended or end early depending on the
level of public participation. Persons
seeking to attend or present at the
public hearing must register by October
19, 2016. Electronic or written
comments will be accepted after the
public hearing until January 9, 2017.
ADDRESSES: The public hearing will be
held at the FDA White Oak Campus,
10903 New Hampshire Ave., Bldg. 31
Conference Center, the Great Room (Rm.
1503), Silver Spring, MD 20993–0002.
Entrance for the public meeting
participants (non-FDA employees) is
through Building 1 where routine
SUMMARY:
PO 00000
Frm 00003
Fmt 4702
Sfmt 4702
60299
security check procedures will be
performed. For parking and security
information, please refer to https://
www.fda.gov/AboutFDA/
WorkingatFDA/BuildingsandFacilities/
WhiteOakCampusInformation/
ucm241740.htm.
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–N–1149 for ‘‘Manufacturer
Communications Regarding
Unapproved Uses of Approved or
Cleared Medical Products; Public
Hearing; Request for Comments.’’
Received comments will be placed in
the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
E:\FR\FM\01SEP1.SGM
01SEP1
Agencies
[Federal Register Volume 81, Number 170 (Thursday, September 1, 2016)]
[Proposed Rules]
[Pages 60298-60299]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-20928]
=======================================================================
-----------------------------------------------------------------------
CONSUMER PRODUCT SAFETY COMMISSION
16 CFR Chapter II
[Docket No. CPSC-2016-0019]
Petition To Amend Statement of Interpretation and Enforcement
Policy Regarding Labeling of Household Products Containing Methylene
Chloride; Request for Comments
AGENCY: Consumer Product Safety Commission.
ACTION: Notice of petition.
-----------------------------------------------------------------------
SUMMARY: The United States Consumer Product Safety Commission (CPSC or
Commission) received a petition requesting that the Commission amend
the agency's 1987 Statement of Interpretation and Enforcement Policy
regarding labeling of household products containing methylene chloride
(Policy Statement). The petition asks the Commission to expand the
Policy Statement to address acute hazards from inhalation of methylene
chloride vapors in addition to the chronic hazards addressed by the
current Policy Statement. The Commission invites written comments
concerning the petition.
DATES: The Office of the Secretary must receive comments on the
petition by October 31, 2016.
ADDRESSES: You may submit comments, identified by Docket No. CPSC-2016-
0019, by any of the following methods:
Electronic Submissions: Submit electronic comments to the Federal
eRulemaking Portal at: https://www.regulations.gov. Follow the
instructions for submitting comments. The Commission does not accept
comments submitted by electronic mail (email), except through
www.regulations.gov. The Commission encourages you to submit electronic
comments by using the Federal eRulemaking Portal, as described above.
Written Submissions: Submit written submissions by mail/hand
delivery/courier to: Office of the Secretary, Consumer Product Safety
Commission, Room 820, 4330 East West Highway, Bethesda, MD 20814;
telephone (301) 504-7923.
Instructions: All submissions received must include the agency name
and docket number for this proposed rulemaking. All comments received
may be posted without change, including any personal identifiers,
contact information, or other personal information provided, to: https://www.regulations.gov. Do not submit confidential business information,
trade secret information, or other sensitive or protected information
that you do not want to be available to the public. If furnished at
all, such information should be submitted in writing.
Docket: For access to the docket to read background documents or
comments received, go to: https://www.regulations.gov, and insert the
docket number, CPSC-2016-0019, into the ``Search'' box, and follow the
prompts. A copy of the petition is available at https://www.regulations.gov under Docket No. CPSC-2016-0019, Supporting and
Related Materials.
[[Page 60299]]
FOR FURTHER INFORMATION CONTACT: Todd Stevenson, Office of the
Secretary, U.S. Consumer Product Safety Commission, Room 820, 4330 East
West Highway, Bethesda, MD 20814; telephone (301) 504-6833.
SUPPLEMENTARY INFORMATION: The Commission received a petition from the
Halogenated Solvents Industry Alliance, Inc. (Petitioner) requesting
that the Commission amend the agency's Statement of Interpretation and
Enforcement Policy regarding labeling of household products containing
methylene chloride (Policy Statement). The Policy Statement provides
the Commission's guidance for labeling of household products containing
methylene chloride, focusing particularly on paint strippers. 52 FR
34698 (Sep. 14, 1987). The Policy Statement sets forth general
principles and examples for labeling to warn consumers of potential
cancer hazards; it does not address acute hazards.
The Petitioner asks the Commission to expand the Policy Statement
to address acute hazards from inhalation of methylene chloride vapors.
Petitioner notes that the Occupational Safety and Health Administration
(OSHA) and the National Institute for Occupational Safety and Health
(NIOSH) issued a Hazard Alert identifying at least 14 deaths associated
with use of methylene chloride-containing paint strippers by
professional bathtub refinishing operations (https://www.osha.gov/dts/hazardalerts/methylene_chloride_hazard_alert.html). Although the
Petitioner refers to incidents involving workers, as the Commission's
Policy Statement indicates, methylene chloride paint strippers are
household products available for consumers to purchase and use.
Petitioner asserts that revising the Policy Statement to give specific
guidance on labeling for the acute hazard posed by inhalation of
methylene chloride vapors, particularly when used in an enclosed space,
such as when refinishing bathtubs, would help to prevent future
fatalities.
By this notice, the Commission seeks comments concerning this
petition. Interested parties may obtain a copy of the petition from the
Commission's Web site: https://www.cpsc.gov/Regulations-Laws--Standards/Rulemaking/Petitions/ or by writing or calling the Office of the
Secretary, U.S. Consumer Product Safety Commission, Room 820, 4330 East
West Highway, Bethesda, MD 20814; telephone (301) 504-7923. A copy of
the petition is also available for viewing under ``Supporting and
Related Materials'' in: www.regulations.gov, under Docket No. CPSC-
2016-0019 .
Dated: August 2, 2016.
Todd A. Stevenson,
Secretary, U.S. Consumer Product Safety Commission.
[FR Doc. 2016-20928 Filed 8-31-16; 8:45 am]
BILLING CODE 6355-01-P