Color Additive Certification; Increase in Fees for Certification Services, 15755-15756 [05-6155]
Download as PDF
Federal Register / Vol. 70, No. 59 / Tuesday, March 29, 2005 / Rules and Regulations
PART 71—DESIGNATION OF CLASS A,
CLASS B, CLASS C, CLASS D AND
CLASS E AIRSPACE AREAS;
AIRWAYS; ROUTES; AND REPORTING
POINTS
1. The authority citation for 14 CFR
part 71 continues to read as follows:
I
Authority: 49 U.S.C. 106(g); 40103, 40113,
40120; EO 10854, 24 FR 9565, 3 CFR, 1959–
1963 Comp., p. 389; 14 CFR 11.69.
§ 71.1
Amended
2. The incorporation by reference in 14
CFR 71.1 of Federal Aviation
Administration Order 7400.9M,
Airspace Designations and Reporting
Points, dated August 30, 2004, and
effective September 16, 2004, is
amended as follows:
I
Paragraph 6004 Class E4 Airspace Areas
Designated as an Extension to a Class D or
Class E Surface Area.
*
*
*
*
*
ASO FL E4 Cocoa Beach Patrick AFB, FL
[NEW]
Cocoa Beach, Patrick Air Force Base, FL
(Lat. 28°14′06″ N, long. 80°36′36″ W)
That airspace extending upward from the
surface within 3.4 miles each side of the
Patrick TACAN 034° radial, extending from
the 5.3-mile radius to 7.3 miles northeast of
the airport. This Class E airspace is effective
during the specific days and times
established in advance by a Notice to
Airmen. The effective days and times will
thereafter be continuously published in the
Airport/Facility Directory.
*
*
*
*
*
Issued in College Park, Georgia, on March
11, 2005.
Mark D. Ward,
Acting Area Director, Air Traffic Division,
Southern Region.
[FR Doc. 05–6069 Filed 3–28–05; 8:45 am]
BILLING CODE 4910–13–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 80
[Docket No. 2005N–0077]
Color Additive Certification; Increase
in Fees for Certification Services
AGENCY:
Food and Drug Administration,
HHS.
Interim final rule; opportunity
for public comment.
ACTION:
SUMMARY: The Food and Drug
Administration (FDA) is issuing an
interim final rule to amend the color
additive regulations by increasing the
VerDate jul<14>2003
16:55 Mar 28, 2005
Jkt 205001
fees for certification services. The
change in fees will allow FDA to
continue to maintain an adequate color
certification program as required by the
Federal Food, Drug, and Cosmetic Act
(the act). The fees are intended to
recover the full costs of operation of
FDA’s color certification program.
DATES: The interim final rule is effective
April 28, 2005. Submit written or
electronic comments by May 31, 2005.
ADDRESSES: You may submit comments,
identified by Docket No. 2005N–0077 by
any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Agency Web site: https://
www.fda.gov/dockets/ecomments.
Follow the instructions for submitting
comments on the agency Web site.
• E-mail: fdadockets@oc.fda.gov.
Include Docket No. 2005N–0077 in the
subject line of your e-mail message.
• FAX: 301–827–6870.
• Mail/Hand delivery/Courier [For
paper, disk, or CD–ROM submissions]:
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
Instructions: All submissions received
must include the agency name and
Docket No(s). or Regulatory Information
Number (RIN) for this rulemaking. All
comments received will be posted
without change to https://www.fda.gov/
ohrms/dockets/default.htm, including
any personal information provided. For
detailed instructions on submitting
comments and additional information
on the rulemaking process, see the
‘‘Opportunity for Public Comment’’
heading of the SUPPLEMENTARY
INFORMATION section of this document.
Docket: For access to the docket to
read background documents or
comments received, go to https://
www.fda.gov/ohrms/dockets/
default.htm and insert the docket
number(s), found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Robert MacLeod, Division of Budget
Execution (HFA–140), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–887–3923;
and Theodor J. Dougherty, Division of
Accounting (HFA–120), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–5032.
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00031
Fmt 4700
Sfmt 4700
15755
I. Background
FDA is increasing the fees provided
for in the agency’s regulations for
certifying color additives. This
modification is necessary because of a
general increase in all costs of operating
the certification program.
The fee schedule for color additive
certification is designed to cover all the
costs involved in certifying batches of
color additives. This includes both the
cost of specific tests required by the
regulations and the general costs
associated with the certification
program, such as costs of accounting,
reviewing data, issuing certificates, and
conducting research and establishment
inspections.
Section 721(e) of the act (21 U.S.C.
379(e)) requires that fees necessary to
provide, maintain, and equip an
adequate color additive certification
program be specified in agency
regulations. The current fee schedule
specified in the regulations became
effective in 1994. Since 1994, the costs
of the certification program significantly
increased as a result of escalating staff
payroll, rent and facility charges, as well
as general operational expenses
including equipment.
As is evidenced by the increased costs
incurred since 1994, the current fee
schedule is insufficient to provide,
equip, and maintain an adequate
certification service. Therefore, an
immediate increase is necessary. All
cost estimates are described in the
‘‘2003 Color Certification Fee Study.’’ A
copy of this document is on file at the
Division of Dockets Management (see
ADDRESSES).
II. Effective Date
The agency is issuing this amendment
as an interim final rule effective (see
DATES). The establishment of fees
necessary to provide, equip, and
maintain an adequate certification
service for colors has been mandated by
Congress under section 721(e) of the act.
As certification services are provided to
industry directly by FDA, the setting of
a fee schedule to pay for these services
is a matter particularly within the
purview and expertise of the agency.
The fees established by this regulation
have been based on cost accounting
methods using data compiled by the
agency. Increasing the fees by $0.05 per
pound will ensure the viability of the
certification program and offset the
increased costs of maintaining this
program. The fee for straight colors
including lakes will be $0.35 per pound
(a $0.05 per pound increase) with a
minimum fee of $224. There are similar
increases in fees for repacks of certified
E:\FR\FM\29MRR1.SGM
29MRR1
15756
Federal Register / Vol. 70, No. 59 / Tuesday, March 29, 2005 / Rules and Regulations
color additives and color additive
mixtures.
III. Analysis of Impacts
FDA has examined the impacts of the
interim final rule under Executive Order
12866 and the Regulatory Flexibility Act
(5 U.S.C. 601–612), and the Unfunded
Mandate Reforms Flexibility Act (Public
Law 104–4). Executive Order 12866
directs agencies to assess all costs and
benefits of available regulatory
alternatives and, when regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety,
and other advantages; distributive
impacts; and equity). The agency
believes that this interim final rule is
consistent with the regulatory
philosophy and principles identified in
the Executive order. In addition, the
interim final rule is not a significant
regulatory action as defined by the
Executive order and so is not subject to
review under the Executive order.
The Regulatory Flexibility Act
requires agencies to analyze regulatory
options that would minimize any
significant impact of a rule on small
entities. The entire cost of this fee
increase would be approximately
$849,626 per year and would be
distributed amongst approximately 23
companies who would pay an increased
fee that is proportional to the number of
pounds of color that they certify. The
great majority of these costs will be
borne by a few firms that have a
dominate share of the color certification
market. These firms that have the largest
shares of the market would pay most of
these fees. In addition, by the Small
Business Administration (SBA)
standards, all of the affected
manufacturers of color additives are
considered large. Thus, the agency
certifies that the interim final rule will
not have a significant economic impact
on a substantial number of small
entities. Therefore, under the Regulatory
Flexibility Act, no further analysis is
required.
Section 202(a) of the Unfunded
Mandates Reform Act of 1995 requires
that agencies prepare a written
statement, which includes an
assessment of anticipated costs and
benefits, before proposing ‘‘any rule that
includes any Federal mandate that may
result in the expenditure by State, local,
and tribal governments, in the aggregate,
or by the private sector, of $100,000,000
or more (adjusted annually for inflation)
in any one year.’’ The current threshold
after adjustment for inflation is $115
million, using the most current (2003)
Implicit Price Deflator for the Gross
VerDate jul<14>2003
16:55 Mar 28, 2005
Jkt 205001
Domestic Product. FDA does not expect
this final rule to result in any 1-year
expenditure that would meet or exceed
this amount.
IV. Environmental Impact
The agency has determined under 21
CFR 25.22(a) 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.
V. Opportunity for Public Comment
Under 5 U.S.C. 553(b)(B) and 21 CFR
10.40(e), FDA finds that providing for
notice and public comment before the
establishment of these fees, and for
revising the basis on which these fees
are calculated, is contrary to the public
interest. It is necessary to implement the
fee increase as soon as possible to
preserve adequate funds for the
program. A delay could result in the
fund being exhausted before the end of
the fiscal year. The agency believes,
however, that it is appropriate to invite
and consider public comments on these
requirements.
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) written or electronic
comments regarding this document.
Submit a single copy of electronic
copies or two paper copies of any
mailed comments, except that
individuals may submit one paper copy.
Comments are to be identified with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
List of Subjects in 21 CFR Part 80
Color additives, Cosmetics, Drugs,
Reporting and recordkeeping
requirements.
I Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs, 21 CFR part 80 is
amended as follows:
PART 80—COLOR ADDITIVE
CERTIFICATION
1. The authority citation for 21 CFR
part 80 continues to read as follows:
I
Authority: 21 U.S.C. 371, 379e.
2. Section 80.10 is amended by
revising paragraphs (a) and (b) to read as
follows:
I
§ 80.10
Fees for certification services.
(a) Fees for straight colors including
lakes. The fee for the services provided
PO 00000
Frm 00032
Fmt 4700
Sfmt 4700
by the regulations in this part in the
case of each request for certification
submitted in accordance with
§ 80.21(j)(1) and (j)(2) shall be $0.35 per
pound of the batch covered by such
requests, but no such fee shall be less
than $224.
(b) Fees for repacks of certified color
additives and color additive mixtures.
The fees for the services provided under
the regulations in this part in the case
of each request for certification
submitted in accordance with
§ 80.21(j)(3) and (j)(4) shall be:
(1) 100 pounds or less—$35.
(2) Over 100 pounds but not over
1,000 pounds—$35 plus $0.05 for each
pound over 100 pounds.
(3) Over 1,000 pounds—$89 plus
$0.02 for each pound over 1,000
pounds.
*
*
*
*
*
Dated: March 21, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05–6155 Filed 3–28–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 172
[Docket No. 2003F–0471]
Food Additives Permitted for Direct
Addition to Food for Human
Consumption; Glycerol Ester of Gum
Rosin
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Final rule.
SUMMARY: The Food and Drug
Administration (FDA) is amending the
food additive regulations to provide for
the safe use of glycerol ester of gum
rosin (GEGR) to adjust the density of
citrus oils used in the preparation of
beverages. This action is in response to
a petition filed by T&R Chemicals, Inc.
DATES: This rule is effective March 29,
2005. Submit written or electronic
objections and requests for a hearing by
April 28, 2005.
ADDRESSES: You may submit written or
electronic objections and requests for a
hearing, identified by Docket No.
2003F–0471, by any of the following
methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Agency Web site: https://
www.fda.gov/dockets/ecomments.
E:\FR\FM\29MRR1.SGM
29MRR1
Agencies
[Federal Register Volume 70, Number 59 (Tuesday, March 29, 2005)]
[Rules and Regulations]
[Pages 15755-15756]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-6155]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 80
[Docket No. 2005N-0077]
Color Additive Certification; Increase in Fees for Certification
Services
AGENCY: Food and Drug Administration, HHS.
ACTION: Interim final rule; opportunity for public comment.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is issuing an interim
final rule to amend the color additive regulations by increasing the
fees for certification services. The change in fees will allow FDA to
continue to maintain an adequate color certification program as
required by the Federal Food, Drug, and Cosmetic Act (the act). The
fees are intended to recover the full costs of operation of FDA's color
certification program.
DATES: The interim final rule is effective April 28, 2005. Submit
written or electronic comments by May 31, 2005.
ADDRESSES: You may submit comments, identified by Docket No. 2005N-0077
by any of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Agency Web site: https://www.fda.gov/dockets/ecomments.
Follow the instructions for submitting comments on the agency Web site.
E-mail: fdadockets@oc.fda.gov. Include Docket No. 2005N-
0077 in the subject line of your e-mail message.
FAX: 301-827-6870.
Mail/Hand delivery/Courier [For paper, disk, or CD-ROM
submissions]: Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Instructions: All submissions received must include the agency name
and Docket No(s). or Regulatory Information Number (RIN) for this
rulemaking. All comments received will be posted without change to
https://www.fda.gov/ohrms/dockets/default.htm, including any personal
information provided. For detailed instructions on submitting comments
and additional information on the rulemaking process, see the
``Opportunity for Public Comment'' heading of the SUPPLEMENTARY
INFORMATION section of this document.
Docket: For access to the docket to read background documents or
comments received, go to https://www.fda.gov/ohrms/dockets/default.htm
and insert the docket number(s), found in brackets in the heading of
this document, into the ``Search'' box and follow the prompts and/or go
to the Division of Dockets Management, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Robert MacLeod, Division of Budget
Execution (HFA-140), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-887-3923; and Theodor J. Dougherty, Division
of Accounting (HFA-120), Food and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301-827-5032.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is increasing the fees provided for in the agency's regulations
for certifying color additives. This modification is necessary because
of a general increase in all costs of operating the certification
program.
The fee schedule for color additive certification is designed to
cover all the costs involved in certifying batches of color additives.
This includes both the cost of specific tests required by the
regulations and the general costs associated with the certification
program, such as costs of accounting, reviewing data, issuing
certificates, and conducting research and establishment inspections.
Section 721(e) of the act (21 U.S.C. 379(e)) requires that fees
necessary to provide, maintain, and equip an adequate color additive
certification program be specified in agency regulations. The current
fee schedule specified in the regulations became effective in 1994.
Since 1994, the costs of the certification program significantly
increased as a result of escalating staff payroll, rent and facility
charges, as well as general operational expenses including equipment.
As is evidenced by the increased costs incurred since 1994, the
current fee schedule is insufficient to provide, equip, and maintain an
adequate certification service. Therefore, an immediate increase is
necessary. All cost estimates are described in the ``2003 Color
Certification Fee Study.'' A copy of this document is on file at the
Division of Dockets Management (see ADDRESSES).
II. Effective Date
The agency is issuing this amendment as an interim final rule
effective (see DATES). The establishment of fees necessary to provide,
equip, and maintain an adequate certification service for colors has
been mandated by Congress under section 721(e) of the act. As
certification services are provided to industry directly by FDA, the
setting of a fee schedule to pay for these services is a matter
particularly within the purview and expertise of the agency. The fees
established by this regulation have been based on cost accounting
methods using data compiled by the agency. Increasing the fees by $0.05
per pound will ensure the viability of the certification program and
offset the increased costs of maintaining this program. The fee for
straight colors including lakes will be $0.35 per pound (a $0.05 per
pound increase) with a minimum fee of $224. There are similar increases
in fees for repacks of certified
[[Page 15756]]
color additives and color additive mixtures.
III. Analysis of Impacts
FDA has examined the impacts of the interim final rule under
Executive Order 12866 and the Regulatory Flexibility Act (5 U.S.C. 601-
612), and the Unfunded Mandate Reforms Flexibility Act (Public Law 104-
4). Executive Order 12866 directs agencies to assess all costs and
benefits of available regulatory alternatives and, when regulation is
necessary, to select regulatory approaches that maximize net benefits
(including potential economic, environmental, public health and safety,
and other advantages; distributive impacts; and equity). The agency
believes that this interim final rule is consistent with the regulatory
philosophy and principles identified in the Executive order. In
addition, the interim final rule is not a significant regulatory action
as defined by the Executive order and so is not subject to review under
the Executive order.
The Regulatory Flexibility Act requires agencies to analyze
regulatory options that would minimize any significant impact of a rule
on small entities. The entire cost of this fee increase would be
approximately $849,626 per year and would be distributed amongst
approximately 23 companies who would pay an increased fee that is
proportional to the number of pounds of color that they certify. The
great majority of these costs will be borne by a few firms that have a
dominate share of the color certification market. These firms that have
the largest shares of the market would pay most of these fees. In
addition, by the Small Business Administration (SBA) standards, all of
the affected manufacturers of color additives are considered large.
Thus, the agency certifies that the interim final rule will not have a
significant economic impact on a substantial number of small entities.
Therefore, under the Regulatory Flexibility Act, no further analysis is
required.
Section 202(a) of the Unfunded Mandates Reform Act of 1995 requires
that agencies prepare a written statement, which includes an assessment
of anticipated costs and benefits, before proposing ``any rule that
includes any Federal mandate that may result in the expenditure by
State, local, and tribal governments, in the aggregate, or by the
private sector, of $100,000,000 or more (adjusted annually for
inflation) in any one year.'' The current threshold after adjustment
for inflation is $115 million, using the most current (2003) Implicit
Price Deflator for the Gross Domestic Product. FDA does not expect this
final rule to result in any 1-year expenditure that would meet or
exceed this amount.
IV. Environmental Impact
The agency has determined under 21 CFR 25.22(a) 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.
V. Opportunity for Public Comment
Under 5 U.S.C. 553(b)(B) and 21 CFR 10.40(e), FDA finds that
providing for notice and public comment before the establishment of
these fees, and for revising the basis on which these fees are
calculated, is contrary to the public interest. It is necessary to
implement the fee increase as soon as possible to preserve adequate
funds for the program. A delay could result in the fund being exhausted
before the end of the fiscal year. The agency believes, however, that
it is appropriate to invite and consider public comments on these
requirements.
Interested persons may submit to the Division of Dockets Management
(see ADDRESSES) written or electronic comments regarding this document.
Submit a single copy of electronic copies or two paper copies of any
mailed comments, except that individuals may submit one paper copy.
Comments are to be identified with the docket number found in brackets
in the heading of this document. Received comments may be seen in the
Division of Dockets Management between 9 a.m. and 4 p.m., Monday
through Friday.
List of Subjects in 21 CFR Part 80
Color additives, Cosmetics, Drugs, Reporting and recordkeeping
requirements.
0
Therefore, under the Federal Food, Drug, and Cosmetic Act and under
authority delegated to the Commissioner of Food and Drugs, 21 CFR part
80 is amended as follows:
PART 80--COLOR ADDITIVE CERTIFICATION
0
1. The authority citation for 21 CFR part 80 continues to read as
follows:
Authority: 21 U.S.C. 371, 379e.
0
2. Section 80.10 is amended by revising paragraphs (a) and (b) to read
as follows:
Sec. 80.10 Fees for certification services.
(a) Fees for straight colors including lakes. The fee for the
services provided by the regulations in this part in the case of each
request for certification submitted in accordance with Sec.
80.21(j)(1) and (j)(2) shall be $0.35 per pound of the batch covered by
such requests, but no such fee shall be less than $224.
(b) Fees for repacks of certified color additives and color
additive mixtures. The fees for the services provided under the
regulations in this part in the case of each request for certification
submitted in accordance with Sec. 80.21(j)(3) and (j)(4) shall be:
(1) 100 pounds or less--$35.
(2) Over 100 pounds but not over 1,000 pounds--$35 plus $0.05 for
each pound over 100 pounds.
(3) Over 1,000 pounds--$89 plus $0.02 for each pound over 1,000
pounds.
* * * * *
Dated: March 21, 2005.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 05-6155 Filed 3-28-05; 8:45 am]
BILLING CODE 4160-01-S