Semipostal Stamp Program, 6764-6765 [05-2467]
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Federal Register / Vol. 70, No. 26 / Wednesday, February 9, 2005 / Rules and Regulations
(b) Secondary credit. The interest
rates for secondary credit provided to
depository institutions under § 201.4(b)
are:
Federal Reserve
Bank
Rate
Boston ....................
New York ................
Philadelphia ............
Cleveland ................
Richmond ...............
Atlanta ....................
Chicago ..................
St. Louis .................
Minneapolis ............
Kansas City ............
Dallas ......................
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Effective
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2005.
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By order of the Board of Governors of the
Federal Reserve System, February 3, 2005.
Jennifer J. Johnson,
Secretary of the Board.
[FR Doc. 05–2463 Filed 2–8–05; 8:45 am]
BILLING CODE 6210–02–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 522
Implantation or Injectable Dosage
Form New Animal Drugs; Zeranol
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final rule.
SUMMARY: The Food and Drug
Administration (FDA) is amending the
animal drug regulations to reflect
approval of two supplemental new
animal drug applications (NADAs) filed
by Schering-Plough Animal Health
Corp. The supplemental NADAs
provide for the addition of statements to
labeling of subcutaneous implants
containing zeranol warning against the
use of these products in calves to be
processed for veal.
DATES: This rule is effective February 9,
2005.
FOR FURTHER INFORMATION CONTACT: Eric
S. Dubbin, Center for Veterinary
Medicine (HFV–126), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 301–827–0232, email: edubbin@cvm.fda.gov.
SUPPLEMENTARY INFORMATION: ScheringPlough Animal Health Corp., 1095
Morris Ave., Union, NJ 07083, filed a
supplement to NADA 38–233 for
RALGRO (zeranol) and to NADA 141–
192 for RALGRO LA (zeranol), two
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14:47 Feb 08, 2005
Jkt 205001
subcutaneous implants/products used
in certain classes of cattle or in sheep
for improved feed efficiency and/or
increased rate of weight gain. The
supplemental NADAs provide for the
addition of statements to labeling
warning against the use of these
products in calves to be processed for
veal. The supplemental applications are
approved as of January 14, 2005, and the
regulations are amended in 21 CFR
522.2680 to reflect the approval. The
basis of approval is discussed in the
freedom of information summaries.
In accordance with the freedom of
information provisions of 21 CFR part
20 and 21 CFR 514.11(e)(2)(ii),
summaries of safety and effectiveness
data and information submitted to
support approval of these applications
may be seen in the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852, between 9
a.m. and 4 p.m., Monday through
Friday.
The agency has determined under 21
CFR 25.33(a)(1) that this action is of a
type that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
nor an environmental impact statement
is required.
This rule does not meet the definition
of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because
it is a rule of ‘‘particular applicability.’’
Therefore, it is not subject to the
congressional review requirements in 5
U.S.C. 801–808.
List of Subjects in 21 CFR Part 522
Animal drugs.
I Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs and redelegated to the
Center for Veterinary Medicine, 21 CFR
part 522 is amended as follows:
PART 522—IMPLANTATION OR
INJECTABLE DOSAGE FORM NEW
ANIMAL DRUGS
1. The authority citation for 21 CFR
part 522 continues to read as follows:
I
Authority: 21 U.S.C. 360b.
2. Section 522.2680 is amended by
revising paragraphs (d)(1)(iii), (d)(2)(iii),
(d)(3)(iii), and (d)(4)(iii) to read as
follows:
I
§ 522.2680
Zeranol.
*
*
*
*
*
(d) * * *
(1) * * *
(iii) Limitations. Implant
subcutaneously in ear only. Do not use
in bulls intended for reproduction or in
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dairy animals. Do not use before 1
month of age or after weaning in heifers
intended for reproduction. Safety and
effectiveness have not been established
in veal calves. A withdrawal period has
not been established for this product in
preruminating calves. Do not use in
calves to be processed for veal.
(2) * * *
(iii) Limitations. Implant
subcutaneously in ear only. Do not use
in breeding animals. Do not implant
animals within 40 days of slaughter.
Safety and effectiveness have not been
established in veal calves. A withdrawal
period has not been established for this
product in preruminating calves. Do not
use in calves to be processed for veal.
(3) * * *
(iii) Limitations. Implant
subcutaneously in ear only. Safety and
effectiveness have not been established
in veal calves. A withdrawal period has
not been established for this product in
preruminating calves. Do not use in
calves to be processed for veal.
(4) * * *
(iii) Limitations. Implant
subcutaneously in ear only. Safety and
effectiveness have not been established
in veal calves. A withdrawal period has
not been established for this product in
preruminating calves. Do not use in
calves to be processed for veal.
Dated: January 27, 2005.
Steven D. Vaughn,
Director, Office of New Animal Drug
Evaluation, Center for Veterinary Medicine.
[FR Doc. 05–2451 Filed 2–8–05; 8:45 am]
BILLING CODE 4160–01–S
POSTAL SERVICE
39 CFR Part 551
Semipostal Stamp Program
Postal Service.
Final rule.
AGENCY:
ACTION:
SUMMARY: This final rule clarifies
regulations relating to the determination
of costs to be offset from differential
revenue.
DATES: The final rule is effective
February 9, 2005.
FOR FURTHER INFORMATION CONTACT:
Cindy Tackett, (703) 292–3980.
SUPPLEMENTARY INFORMATION:
Semipostal stamps are intended to raise
funds for specified causes. The
difference between the sales price of a
semipostal stamp and its postage value
(the differential) constitutes a
contribution to a specified cause. The
Postal Service is permitted to retain an
amount from the differential to cover its
reasonable administrative costs.
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Federal Register / Vol. 70, No. 26 / Wednesday, February 9, 2005 / Rules and Regulations
Section 551.8 sets forth the Postal
Service’s policy to recover from the
differential those costs determined to be
attributable to the semipostal and that
would not normally be incurred for
commemorative stamps having similar
sales objectives; physical characteristics;
and marketing, promotional, and public
relations activities. Under current
regulations published in 39 CFR 551.8:
(e) Cost items recoverable from the
differential revenue may include, but are not
limited to, the following:
(1) Packaging costs in excess of the cost to
package comparable stamps;
(2) Printing costs of flyers and special
receipts;
(3) Costs of changes to equipment;
(4) Costs of developing and executing
marketing and promotional plans in excess of
the cost for comparable stamps;
(5) Other costs specific to the semipostal
stamp that would not normally have been
incurred for comparable stamps; and
(6) Costs in paragraph (g) of this section
that materially exceed those that would
normally have been incurred for comparable
stamps.
The final rule deletes the word ‘‘may’’
from the introductory paragraph to
subsection (e) of 39 CFR 551.8. The
deletion of the word ‘‘may’’ clarifies that
costs that are recovered from the
differential include, but are not limited
to, packaging costs in excess of those for
comparable stamps, printing costs for
flyers or special receipts, costs of
changes to equipment, costs of
developing and executing marketing
and promotional plans in excess of
those for comparable stamps, and other
costs that would not normally have been
incurred for comparable stamps.
List of Subjects in 39 CFR Part 551
Administrative practice and
procedure, Postal Service.
The Amendment
For the reasons set out in this
document, the Postal Service hereby
amends 39 CFR part 551 as follows:
I
PART 551—SEMIPOSTAL STAMP
PROGRAM
1. The authority citation for 39 CFR
part 551 continues to read as follows:
I
Authority: 39 U.S.C. 101, 201, 203, 401,
403, 404, 410, 414, 416.
2. Revise paragraph (e) introductory
text in § 551.8 to read as follows:
I
§ 551.8
*
Cost offset policy.
*
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*
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Jkt 205001
(e) Cost items recoverable from the
differential revenue include, but are not
limited to, the following:
*
*
*
*
*
Neva Watson,
Attorney, Legislative.
[FR Doc. 05–2467 Filed 2–8–05; 8:45 am]
BILLING CODE 7710–12–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 271
[FRL–7870–2]
South Carolina: Final Authorization of
State Hazardous Waste Management
Program Revision
Environmental Protection
Agency (EPA).
ACTION: Immediate final rule.
AGENCY:
SUMMARY: South Carolina has applied to
EPA for Final authorization of the
changes to its hazardous waste program
under the Resource Conservation and
Recovery Act (RCRA). EPA has
determined that these changes satisfy all
requirements needed to qualify for Final
authorization, and is authorizing the
State’s changes through this immediate
final action. EPA is publishing this rule
to authorize the changes without a prior
proposal because we believe this action
is not controversial and do not expect
comments that oppose it. Unless we get
written comments which oppose this
authorization during the comment
period, the decision to authorize South
Carolina’s changes to their hazardous
waste program will take effect. If we get
comments that oppose this action, we
will publish a document in the Federal
Register withdrawing this rule before it
takes effect and a separate document in
the proposed rules section of this
Federal Register will serve as a proposal
to authorize the changes.
DATES: This Final authorization will
become effective on April 11, 2005,
unless EPA receives adverse written
comment by March 11, 2005. If EPA
receives such comment, it will publish
a timely withdrawal of this immediate
final rule in the Federal Register and
inform the public that this authorization
will not take effect.
ADDRESSES: Send written comments to
Thornell Cheeks, South Carolina
Authorizations Coordinator, RCRA
Programs Branch, Waste Management
Division, U.S. Environmental Protection
Agency, Atlanta Federal Center, 61
Forsyth Street, SW., Atlanta, GA 30303–
3104; (404) 562–8479. The application
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6765
can be viewed electronically at https://
www.regulation.gov. Electronic
comments on the application can be
made from this site. You may also email your comments to
Cheeks.Thornell@epa.gov. You can view
and copy South Carolina’s applications
from 9 a.m. to 4 p.m. at the following
addresses: South Carolina Department
of Health and Environmental Control,
2600 Bull Street, Columbia, South
Carolina 29201, (803) 896–4174; and
EPA Region 4, Atlanta Federal Center,
Library, 61 Forsyth Street, SW., Atlanta,
Georgia 30303; (404) 562–8190, John
Wright, Librarian.
FOR FURTHER INFORMATION CONTACT:
Thornell Cheeks, South Carolina
Authorizations Coordinator, RCRA
Programs Branch, Waste Management
Division, U.S. Environmental Protection
Agency, Atlanta Federal Center, 61
Forsyth Street, SW., Atlanta, GA 30303–
3104; (404) 562–8479.
SUPPLEMENTARY INFORMATION:
A. Why Are Revisions to State
Programs Necessary?
States which have received final
authorization from EPA under RCRA
section 3006(b), 42 U.S.C. 6926(b), must
maintain a hazardous waste program
that is equivalent to, consistent with,
and no less stringent than the Federal
program. As the Federal program
changes, States must change their
programs and ask EPA to authorize the
changes. Changes to State programs may
be necessary when Federal or State
statutory or regulatory authority is
modified or when certain other changes
occur. Most commonly, States must
change their programs because of
changes to EPA’s regulations in 40 Code
of Federal Regulations (CFR) parts 124,
260 through 266, 268, 270, 273 and 279.
B. What Decisions Have We Made in
This Rule?
We conclude that South Carolina’s
applications to revise its authorized
program meets all of the statutory and
regulatory requirements established by
RCRA. Therefore, we grant South
Carolina Final authorization to operate
its hazardous waste program with the
changes described in the authorization
applications. South Carolina has
responsibility for permitting Treatment,
Storage, and Disposal Facilities (TSDFs)
within its borders (except in Indian
Country) and for carrying out the
aspects of the RCRA program described
in its revised program application,
subject to the limitations of the
Hazardous and Solid Waste
Amendments of 1984 (HSWA). New
Federal requirements and prohibitions
E:\FR\FM\09FER1.SGM
09FER1
]]>Agencies
[Federal Register Volume 70, Number 26 (Wednesday, February 9, 2005)]
[Rules and Regulations]
[Pages 6764-6765]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-2467]
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POSTAL SERVICE
39 CFR Part 551
Semipostal Stamp Program
AGENCY: Postal Service.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: This final rule clarifies regulations relating to the
determination of costs to be offset from differential revenue.
DATES: The final rule is effective February 9, 2005.
FOR FURTHER INFORMATION CONTACT: Cindy Tackett, (703) 292-3980.
SUPPLEMENTARY INFORMATION: Semipostal stamps are intended to raise
funds for specified causes. The difference between the sales price of a
semipostal stamp and its postage value (the differential) constitutes a
contribution to a specified cause. The Postal Service is permitted to
retain an amount from the differential to cover its reasonable
administrative costs.
[[Page 6765]]
Section 551.8 sets forth the Postal Service's policy to recover
from the differential those costs determined to be attributable to the
semipostal and that would not normally be incurred for commemorative
stamps having similar sales objectives; physical characteristics; and
marketing, promotional, and public relations activities. Under current
regulations published in 39 CFR 551.8:
(e) Cost items recoverable from the differential revenue may
include, but are not limited to, the following:
(1) Packaging costs in excess of the cost to package comparable
stamps;
(2) Printing costs of flyers and special receipts;
(3) Costs of changes to equipment;
(4) Costs of developing and executing marketing and promotional
plans in excess of the cost for comparable stamps;
(5) Other costs specific to the semipostal stamp that would not
normally have been incurred for comparable stamps; and
(6) Costs in paragraph (g) of this section that materially
exceed those that would normally have been incurred for comparable
stamps.
The final rule deletes the word ``may'' from the introductory
paragraph to subsection (e) of 39 CFR 551.8. The deletion of the word
``may'' clarifies that costs that are recovered from the differential
include, but are not limited to, packaging costs in excess of those for
comparable stamps, printing costs for flyers or special receipts, costs
of changes to equipment, costs of developing and executing marketing
and promotional plans in excess of those for comparable stamps, and
other costs that would not normally have been incurred for comparable
stamps.
List of Subjects in 39 CFR Part 551
Administrative practice and procedure, Postal Service.
The Amendment
0
For the reasons set out in this document, the Postal Service hereby
amends 39 CFR part 551 as follows:
PART 551--SEMIPOSTAL STAMP PROGRAM
0
1. The authority citation for 39 CFR part 551 continues to read as
follows:
Authority: 39 U.S.C. 101, 201, 203, 401, 403, 404, 410, 414,
416.
0
2. Revise paragraph (e) introductory text in Sec. 551.8 to read as
follows:
Sec. 551.8 Cost offset policy.
* * * * *
(e) Cost items recoverable from the differential revenue include,
but are not limited to, the following:
* * * * *
Neva Watson,
Attorney, Legislative.
[FR Doc. 05-2467 Filed 2-8-05; 8:45 am]
BILLING CODE 7710-12-P
