Listing of Color Additives Exempt From Certification; Astaxanthin Dimethyldisuccinate; Confirmation of Effective Date, 5887 [2010-2522]
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Federal Register / Vol. 75, No. 24 / Friday, February 5, 2010 / Rules and Regulations
notice is given that no objections or
requests for a hearing were filed in
response to the November 16, 2009,
final rule. Accordingly, the amendments
issued thereby became effective
December 17, 2009.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 73
Dated: January 22, 2010.
Mitchell A. Cheeseman,
Acting Director, Office of Food Additive
Safety, Center for Food Safety and Applied
Nutrition.
[Docket No. FDA–2007–C–0456] (formerly
Docket No. 2007C–0245)
Listing of Color Additives Exempt
From Certification; Paracoccus
Pigment; Confirmation of Effective
Date
AGENCY:
[FR Doc. 2010–2521 Filed 2–4–10; 8:45 am]
BILLING CODE 4160–01–S
Food and Drug Administration,
HHS.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ACTION: Final rule; confirmation of
effective date.
SUMMARY: The Food and Drug
Administration (FDA) is confirming the
effective date of December 17, 2009, for
the final rule that appeared in the
Federal Register of November 16, 2009.
The final rule amended the color
additive regulations to provide for the
safe use of paracoccus pigment as a
color additive in the feed of salmonid
fish to enhance the color of their flesh.
DATES: The effective date for the final
rule that published in the Federal
Register on November 16, 2009 (74 FR
58843) is confirmed as December 17,
2009.
Mical E. Honigfort, Center for Food
Safety and Applied Nutrition (HFS–
265), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park,
MD 20740–3835, 301–436–1278.
SUPPLEMENTARY INFORMATION: In the
Federal Register of November 16, 2009
(74 FR 58843), FDA amended the color
additive regulations to add 21 CFR
73.352 to provide for the safe use of
paracoccus pigment as a color additive
in the feed of salmonid fish to enhance
the color of their flesh.
FDA gave interested persons until
December 16, 2009, to file objections or
requests for a hearing. The agency
received no objections or requests for a
hearing on the final rule. Therefore,
FDA finds that the effective date of the
final rule that published in the Federal
Register of November 16, 2009, should
be confirmed.
WReier-Aviles on DSKGBLS3C1PROD with RULES
List of Subjects in 21 CFR Part 73
Color additives, Cosmetics, Drugs,
Medical devices.
■ Therefore, under the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 321,
341, 342, 343, 348, 351, 352, 355, 361,
362, 371, 379e) and under authority
delegated to the Commissioner of Food
and Drugs, and redelegated to the
Director, Office of Food Additive Safety,
14:20 Feb 04, 2010
Jkt 220001
21 CFR Part 73
[Docket No. FDA–2007–C–0044] (formerly
Docket No. 2007C–0474)
Listing of Color Additives Exempt
From Certification; Astaxanthin
Dimethyldisuccinate; Confirmation of
Effective Date
AGENCY:
HHS.
Final rule; confirmation of
effective date.
ACTION:
The Food and Drug
Administration (FDA) is confirming the
effective date of December 8, 2009, for
the final rule that appeared in the
Federal Register of November 5, 2009.
The final rule amended the color
additive regulations to provide for the
safe use of astaxanthin
dimethyldisuccinate as a color additive
in the feed of salmonid fish to enhance
the color of their flesh.
DATES: The effective date for the final
rule published in the Federal Register
of November 5, 2009 (74 FR 57248) is
confirmed as December 8, 2009.
FOR FURTHER INFORMATION CONTACT:
Felicia M. Ellison, Center for Food
Safety and Applied Nutrition (HFS–
265), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park,
MD 20740–3835, 301–436–1264.
SUPPLEMENTARY INFORMATION: In the
Federal Register of November 5, 2009
(74 FR 57248), FDA amended the color
additive regulations to add § 73.37 (21
CFR 73.37) to provide for the safe use
of astaxanthin dimethyldisuccinate as a
color additive in the feed of salmonid
fish to enhance the color of their flesh.
FDA gave interested persons until
December 7, 2009, to file objections or
requests for a hearing. The agency
received no objections or requests for a
hearing on the final rule. Therefore,
PO 00000
FDA finds that the effective date of the
final rule that published in the Federal
Register of November 5, 2009, should be
confirmed.
List of Subjects in 21 CFR Part 73
Color additives, Cosmetics, Drugs,
Medical devices.
■ Therefore, under the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 321,
341, 342, 343, 348, 351, 352, 355, 361,
362, 371, 379e) and under authority
delegated to the Commissioner of Food
and Drugs, and redelegated to the
Director, Office of Food Additive Safety,
notice is given that no objections or
requests for a hearing were filed in
response to the November 5, 2009, final
rule. Accordingly, the amendments
issued thereby became effective
December 8, 2009.
Dated: January 22, 2010.
Mitchell A. Cheeseman,
Acting Director, Office of Food Additive
Safety, Center for Food Safety and Applied
Nutrition.
[FR Doc. 2010–2522 Filed 2–4–10; 8:45 am]
BILLING CODE 4160–01–S
Food and Drug Administration,
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
VerDate Nov<24>2008
Food and Drug Administration
5887
Frm 00011
Fmt 4700
Sfmt 4700
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 558
[Docket No. FDA–2010–N–0002]
New Animal Drugs for Use in Animal
Feeds; Ractopamine; Monensin
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 an original new animal drug
application (NADA) filed by Elanco
Animal Health, A Division of Eli Lilly
& Co. The NADA provides for use of
single-ingredient Type A medicated
articles containing ractopamine
hydrochloride and monensin to
formulate two-way combination Type C
medicated feeds for finishing hen and
tom turkeys.
DATES: This rule is effective February 5,
2010.
FOR FURTHER INFORMATION CONTACT:
Linda M. Wilmot, Center for Veterinary
Medicine (HFV–120), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240–276–8101, email: linda.wilmot@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Elanco
Animal Health, A Division of Eli Lilly
E:\FR\FM\05FER1.SGM
05FER1
Agencies
[Federal Register Volume 75, Number 24 (Friday, February 5, 2010)]
[Rules and Regulations]
[Page 5887]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-2522]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 73
[Docket No. FDA-2007-C-0044] (formerly Docket No. 2007C-0474)
Listing of Color Additives Exempt From Certification; Astaxanthin
Dimethyldisuccinate; Confirmation of Effective Date
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; confirmation of effective date.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is confirming the
effective date of December 8, 2009, for the final rule that appeared in
the Federal Register of November 5, 2009. The final rule amended the
color additive regulations to provide for the safe use of astaxanthin
dimethyldisuccinate as a color additive in the feed of salmonid fish to
enhance the color of their flesh.
DATES: The effective date for the final rule published in the Federal
Register of November 5, 2009 (74 FR 57248) is confirmed as December 8,
2009.
FOR FURTHER INFORMATION CONTACT: Felicia M. Ellison, Center for Food
Safety and Applied Nutrition (HFS-265), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park, MD 20740-3835, 301-436-1264.
SUPPLEMENTARY INFORMATION: In the Federal Register of November 5, 2009
(74 FR 57248), FDA amended the color additive regulations to add Sec.
73.37 (21 CFR 73.37) to provide for the safe use of astaxanthin
dimethyldisuccinate as a color additive in the feed of salmonid fish to
enhance the color of their flesh.
FDA gave interested persons until December 7, 2009, to file
objections or requests for a hearing. The agency received no objections
or requests for a hearing on the final rule. Therefore, FDA finds that
the effective date of the final rule that published in the Federal
Register of November 5, 2009, should be confirmed.
List of Subjects in 21 CFR Part 73
Color additives, Cosmetics, Drugs, Medical devices.
0
Therefore, under the Federal Food, Drug, and Cosmetic Act (21 U.S.C.
321, 341, 342, 343, 348, 351, 352, 355, 361, 362, 371, 379e) and under
authority delegated to the Commissioner of Food and Drugs, and
redelegated to the Director, Office of Food Additive Safety, notice is
given that no objections or requests for a hearing were filed in
response to the November 5, 2009, final rule. Accordingly, the
amendments issued thereby became effective December 8, 2009.
Dated: January 22, 2010.
Mitchell A. Cheeseman,
Acting Director, Office of Food Additive Safety, Center for Food Safety
and Applied Nutrition.
[FR Doc. 2010-2522 Filed 2-4-10; 8:45 am]
BILLING CODE 4160-01-S