Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Recordkeeping Requirements for Human Food and Cosmetics Manufactured From, Processed With, or Otherwise Containing, Material from Cattle, 11369 [E7-4455]

Download as PDF 11369 Federal Register / Vol. 72, No. 48 / Tuesday, March 13, 2007 / Notices ESTIMATED ANNUAL REPORTING BURDEN1 No. of Respondents 21 CFR Section 1240.63(a)(2)(ii)(A) and (B) 1 There Annual Frequency per Response 65 Total No. of Responses 1.88 122 Dated: March 6, 2007. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. E7–4454 Filed 3–12–07; 8:45 am] BILLING CODE 4160–01–S BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Food and Drug Administration [Docket No. 2004N–0257] [Docket No. 2006N–0130] Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Food Labeling; Trans Fatty Acids in Nutrition Labeling Food and Drug Administration, HHS. ACTION: 4 488 ACTION: The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Food Labeling; Trans Fatty Acids in Nutrition Labeling’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of the Chief Information Officer (HFA–250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857,301–827– 4659. In the Federal Register of October 12, 2006 (71 FR 60157), the agency announced that the proposed information collection had been submitted to OMB for review and clearance under 44 U.S.C. 3507. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0515. The approval expires on January 31, 2010. A copy of the supporting statement for this information collection is available on the Internet at https://www.fda.gov/ ohrms/dockets. SUPPLEMENTARY INFORMATION: VerDate Aug<31>2005 14:58 Mar 12, 2007 Food and Drug Administration, HHS. Notice. Jkt 211001 Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing that a collection of information entitled ‘‘Recordkeeping Requirements for Human Food and Cosmetics Manufactured From, Processed With, or Otherwise Containing, Material from Cattle’’ has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of the Chief Information Officer (HFA–250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857,301–827– 4659. In the Federal Register of October 11, 2006 (71 FR 59653), the agency announced that the proposed information collection had been submitted to OMB for review and clearance under 44 U.S.C. 3507. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. OMB has now approved the information collection and has assigned OMB control number 0910–0597. The approval expires on January 31, 2010. A copy of the supporting statement for this information collection is available on SUPPLEMENTARY INFORMATION: PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 the Internet at https://www.fda.gov/ ohrms/dockets. Dated: March 6, 2007. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. E7–4455 Filed 3–12–07; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Recordkeeping Requirements for Human Food and Cosmetics Manufactured From, Processed With, or Otherwise Containing, Material from Cattle AGENCY: SUMMARY: cprice-sewell on PROD1PC66 with NOTICES Total Hours are no capital costs or operating and maintenance costs associated with this collection of information. Dated: March 6, 2007. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. E7–4450 Filed 3–12–07; 8:45 am] AGENCY: Hours per Response [Docket No. 2007N–0069] Animal Drug User Fee Act; Public Meeting AGENCY: Food and Drug Administration, HHS. ACTION: Notice of public meeting. The Food and Drug Administration (FDA) is announcing a public meeting on the Animal Drug User Fee Act of 2003 (ADUFA) to seek public comments relative to the program’s overall performance and reauthorization as directed by Congress. Date and Time: The public meeting will be held on April 24, 2007, beginning at 9 a.m. Location: The public meeting will be held at the Food and Drug Administration, 7519 Standish Pl., third floor, rm. A, Rockville, MD 20855. There is parking near the building. Photo identification is required to clear building security. Contact: Aleta Sindelar, Office of the Director (HFV–3), Center for Veterinary Medicine, Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240–276–9004, FAX 240–276–9020, e-mail: aleta.sindelar@fda.hhs.gov. Registration and Requests for Oral Presentations: Registration is not required to attend the meeting. Requests to make an oral presentation at the meeting must be submitted by April 17, 2007, to the contact person. Your request to make a presentation should include the following information: Name, title, firm name, address, telephone, fax number, and e-mail address. We will try to accommodate all persons who wish to make a presentation. The time allotted for E:\FR\FM\13MRN1.SGM 13MRN1

Agencies

[Federal Register Volume 72, Number 48 (Tuesday, March 13, 2007)]
[Notices]
[Page 11369]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-4455]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2004N-0257]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approval; Recordkeeping Requirements for Human 
Food and Cosmetics Manufactured From, Processed With, or Otherwise 
Containing, Material from Cattle

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Recordkeeping Requirements for 
Human Food and Cosmetics Manufactured From, Processed With, or 
Otherwise Containing, Material from Cattle'' has been approved by the 
Office of Management and Budget (OMB) under the Paperwork Reduction Act 
of 1995.

FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of the Chief 
Information Officer (HFA-250), Food and Drug Administration, 5600 
Fishers Lane, Rockville, MD 20857,301-827-4659.

SUPPLEMENTARY INFORMATION: In the Federal Register of October 11, 2006 
(71 FR 59653), the agency announced that the proposed information 
collection had been submitted to OMB for review and clearance under 44 
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not 
required to respond to, a collection of information unless it displays 
a currently valid OMB control number. OMB has now approved the 
information collection and has assigned OMB control number 0910-0597. 
The approval expires on January 31, 2010. A copy of the supporting 
statement for this information collection is available on the Internet 
at https://www.fda.gov/ohrms/dockets.

    Dated: March 6, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7-4455 Filed 3-12-07; 8:45 am]
BILLING CODE 4160-01-S
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