Richard C. Theuer; Withdrawal of Food Additive Petition and Citizen Petition, 51922 [2014-20665]
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51922
Federal Register / Vol. 79, No. 169 / Tuesday, September 2, 2014 / Proposed Rules
DEPARTMENT OF TRANSPORTATION
The food additive petition and
the citizen petition were withdrawn on
July 30, 2014.
17 CFR Parts 270 and 274
[Release No. IC–31184A; File No. S7–07–
11]
RIN 3235–AL02
Removal of Certain References to
Credit Ratings and Amendment to the
Issuer Diversification Requirement in
the Money Market Fund Rule;
Correction
Securities and Exchange
Commission.
ACTION: Re-proposed rule; proposed
rule; correction.
AGENCY:
AGENCY:
DATES:
On August 14, 2014, the
Securities and Exchange Commission
(‘‘Commission’’) published a document
in the Federal Register (79 FR 47986).
The document contained an incorrect
RIN. The Commission is publishing this
document to correct that RIN.
DATES: Effective on September 2, 2014.
FOR FURTHER INFORMATION CONTACT: Erin
C. Loomis, Senior Counsel; Amanda
Hollander Wagner, Senior Counsel;
Penelope W. Saltzman, Senior Special
Counsel; Investment Company
Rulemaking Office, at (202) 551–6792,
Division of Investment Management,
Securities and Exchange Commission,
100 F Street NE., Washington, DC
20549–8549.
SUMMARY:
Correction
In the Federal Register of August 14,
2014, in FR Doc. 2014–17746, on page
47986, in the first column, seventh line,
the RIN is corrected to read as noted
above.
Dated: August 27, 2014.
Kevin M. O’Neill,
Deputy Secretary.
[FR Doc. 2014–20731 Filed 8–29–14; 8:45 am]
BILLING CODE P
FOR FURTHER INFORMATION CONTACT:
Molly A. Harry, Center for Food Safety
and Applied Nutrition (HFS–265), Food
and Drug Administration, 5100 Paint
Branch Pkwy., College Park, MD 20740–
3835, 240–402–1075.
In a notice
published in the Federal Register of
July 19, 2013 (78 FR 43093), we
announced that we had filed a food
additive petition (FAP 3A4798; Docket
No. FDA–2013–F–0700), submitted by
Richard C. Theuer, Ph.D., 7904
Sutterton Ct., Raleigh, NC 27615. The
petition proposed to amend the food
additive regulations in § 172.620 and
172.626 (21 CFR172.620 and 172.626) to
prohibit the use of carrageenan and salts
of carrageenan in infant formula. In
addition, we also announced in the
same document (78 FR 43093), that Dr.
Theuer submitted a citizen petition,
under 21 CFR 10.30, requesting that 21
CFR 182.7255 of the GRAS regulations
be amended to prohibit the use of
Chondrus extract (carrageenin) in infant
formula (Docket No. FDA–2013–P–
0472). Dr. Theuer has now withdrawn
the petitions without prejudice to future
filings (21 CFR 171.7 and 10.30(g)).
SUPPLEMENTARY INFORMATION:
Dated: August 26, 2014.
Dennis M. Keefe,
Director, Office of Food Additive Safety,
Center for Food Safety and Applied Nutrition.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[FR Doc. 2014–20665 Filed 8–29–14; 8:45 am]
BILLING CODE 4164–01–P
21 CFR Parts 172 and 182
mstockstill on DSK4VPTVN1PROD with PROPOSALS
The Food and Drug
Administration (FDA or we) is
announcing the withdrawal, without
prejudice to a future filing, of a food
additive petition (FAP 3A4798)
proposing that the food additive
regulations be amended to prohibit the
use of carrageenan and salts of
carrageenan in infant formula. In
addition, FDA is also announcing the
withdrawal of a citizen petition
requesting that the generally recognized
as safe (GRAS) regulations be amended
to prohibit the use of Chondrus extract
(carrageenin) in infant formula.
SUMMARY:
SECURITIES AND EXCHANGE
COMMISSION
[Docket Nos. FDA–2013–F–0700 and FDA–
2013–P–0472]
Richard C. Theuer; Withdrawal of Food
Additive Petition and Citizen Petition
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Withdrawal of petitions.
VerDate Mar<15>2010
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Federal Highway Administration
23 CFR Part 450
Federal Transit Administration
49 CFR Part 613
[Docket No. FHWA–2013–0037]
RIN 2125–AF52; 2132–AB10
Statewide and Nonmetropolitan
Transportation Planning; Metropolitan
Transportation Planning
Federal Highway
Administration (FHWA), Federal
Transit Administration (FTA);
Department of Transportation (DOT).
ACTION: Notice of proposed rulemaking;
extension of comment period.
The FHWA and FTA are
extending the comment period for a
notice of proposed rulemaking (NPRM)
and request for comments, which was
published on June 2, 2014. The original
comment period is set to close on
September 2, 2014. The extension is
based on concern expressed by the
American Association of State Highway
and Transportation Officials (AASHTO)
that the September 2 closing date does
not provide sufficient time to review
and provide comprehensive comments
on the NPRM. The FHWA and FTA
recognize that others interested in
commenting may have similar concerns
and agrees that the comment period
should be extended. Therefore, the
closing date for comments is changed to
October 2, 2014, which will provide
AASHTO and others interested in
commenting additional time to discuss,
evaluate, and submit responses to the
docket.
DATES: The comment period for the
proposed rule published on June 2, 2014
(79 FR 31784), is extended. Comments
must be received on or before October
2, 2014.
ADDRESSES: Mail or hand deliver
comments to the U.S. Department of
Transportation, Dockets Management
Facility, 1200 New Jersey Avenue SE.,
Washington, DC 20590, or submit
electronically at https://
www.regulations.gov. All comments
should include the docket number that
appears in the heading of this
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Friday, except Federal holidays. Those
desiring notification of receipt of
comments must include a selfSUMMARY:
E:\FR\FM\02SEP1.SGM
02SEP1
Agencies
[Federal Register Volume 79, Number 169 (Tuesday, September 2, 2014)]
[Proposed Rules]
[Page 51922]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-20665]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 172 and 182
[Docket Nos. FDA-2013-F-0700 and FDA-2013-P-0472]
Richard C. Theuer; Withdrawal of Food Additive Petition and
Citizen Petition
AGENCY: Food and Drug Administration, HHS.
ACTION: Withdrawal of petitions.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is announcing the
withdrawal, without prejudice to a future filing, of a food additive
petition (FAP 3A4798) proposing that the food additive regulations be
amended to prohibit the use of carrageenan and salts of carrageenan in
infant formula. In addition, FDA is also announcing the withdrawal of a
citizen petition requesting that the generally recognized as safe
(GRAS) regulations be amended to prohibit the use of Chondrus extract
(carrageenin) in infant formula.
DATES: The food additive petition and the citizen petition were
withdrawn on July 30, 2014.
FOR FURTHER INFORMATION CONTACT: Molly A. Harry, Center for Food Safety
and Applied Nutrition (HFS-265), Food and Drug Administration, 5100
Paint Branch Pkwy., College Park, MD 20740-3835, 240-402-1075.
SUPPLEMENTARY INFORMATION: In a notice published in the Federal
Register of July 19, 2013 (78 FR 43093), we announced that we had filed
a food additive petition (FAP 3A4798; Docket No. FDA-2013-F-0700),
submitted by Richard C. Theuer, Ph.D., 7904 Sutterton Ct., Raleigh, NC
27615. The petition proposed to amend the food additive regulations in
Sec. 172.620 and 172.626 (21 CFR172.620 and 172.626) to prohibit the
use of carrageenan and salts of carrageenan in infant formula. In
addition, we also announced in the same document (78 FR 43093), that
Dr. Theuer submitted a citizen petition, under 21 CFR 10.30, requesting
that 21 CFR 182.7255 of the GRAS regulations be amended to prohibit the
use of Chondrus extract (carrageenin) in infant formula (Docket No.
FDA-2013-P-0472). Dr. Theuer has now withdrawn the petitions without
prejudice to future filings (21 CFR 171.7 and 10.30(g)).
Dated: August 26, 2014.
Dennis M. Keefe,
Director, Office of Food Additive Safety, Center for Food Safety and
Applied Nutrition.
[FR Doc. 2014-20665 Filed 8-29-14; 8:45 am]
BILLING CODE 4164-01-P