Kareem I. Batarseh; Filing of Food Additive Petition, 20145 [05-7727]

Download as PDF Federal Register / Vol. 70, No. 73 / Monday, April 18, 2005 / Notices and financial reports are due 90 days after the close of the project period. VII. Agency Contacts Program Office Contact: Catherine Beck, Administration for Children and Families, Office of Community Services’ Operations Center, 1515 Wilson Boulevard, Suite 100, Arlington, VA 22209, Phone: 1–800–281–9519, Fax: 703–528–0716, E-mail: OCS@lcgnet.com. Grants Management Office Contact: Barbara Ziegler-Johnson, Administration for Children and Families, Office of Grants Management, Division of Discretionary Grants, 370 L’Enfant Promenade, SW., Aerospace Building, Washington, DC 20447–0002, Phone: 1– 800–281–9519, Fax: 703–528–0716, Email: OCS@lcgnet.com. VIII. Other Information Notice: Beginning with FY 2006, the Administration for Children and Families (ACF) will no longer publish grant announcements in the Federal Register. Beginning October 1, 2005 applicants will be able to find a synopsis of all ACF grant opportunities and apply electronically for opportunities via: www.Grants.gov. Applicants will also be able to find the complete text of all ACF grant announcements on the ACF Web site located at: https://www.acf.hhs.gov/ grants/. The FY 2006 President’s budget does not include or propose funding for the Community Food and Nutrition Program. Future funding is based on the availability of Federal funds. Direct federal grants, subaward funds, or contracts under this community Food and Nutrition Program shall not be used to support inherently religious activities such as religious instruction, worship, or proselytization. Therefore, organizations must take steps to separate, in time or location, their inherently religious activities from the services funded under this Program. Regulations pertaining to the prohibition of Federal funds for inherently religious activities can be found on the HHS Web site at https:// www.os.HHS.gov/fbci/waisgate21.pdf. Additional Information about this program and its purpose can be located on the following Web site: https:// www.acf.hhs.gov/programs/ocs. Please reference Section IV.3 for details about acknowledgement of received applications. VerDate jul<14>2003 16:08 Apr 15, 2005 Jkt 205001 20145 Dated: April 7, 2005. Josephine B. Robinson, Director, Office of Community Services. [FR Doc. 05–7461 Filed 4–15–05; 8:45 am] DEPARTMENT OF HEALTH AND HUMAN SERVICES BILLING CODE 4184–01–P [Docket No. 2005D–0091] DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 2005F–0138] Kareem I. Batarseh; Filing of Food Additive Petition AGENCY: Food and Drug Administration, HHS. ACTION: Draft Guidance for Industry on User Fee Waivers for Fixed Dose Combination Products and CoPackaged Human Immunodeficiency Virus Drugs for the President’s Emergency Plan for Acquired Immunodeficiency Syndrome Relief; Availability AGENCY: The Food and Drug Administration (FDA) is announcing that Kareem I. Batarseh has filed a petition proposing that the food additive regulations be amended to provide for the safe use of a mixture of hydrogen peroxide, silver nitrate, phosphoric acid, tartaric acid, glutamic acid, and sodium tripolyphosphate as an antimicrobial agent in bottled drinking water. FOR FURTHER INFORMATION CONTACT: 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: Under the Federal Food, Drug, and Cosmetic Act (sec. 409 (b)(5) (21 U.S.C. 348(b)(5))), notice is given that a food additive petition (FAP 5A4759) has been filed by Kareem I. Batarseh, P.O. Box 8, College Park, MD 20741–0008. The petition proposes to amend the food additive regulations in part 172 Food Additives Permitted For Direct Addition To Food For Human Consumption (21 CFR part 172) to provide for the safe use of a mixture of hydrogen peroxide, silver nitrate, phosphoric acid, tartaric acid, glutamic acid, and sodium tripolyphosphate as an antimicrobial agent in bottled drinking water. The agency has determined under 21 CFR 25.32(k) 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. Dated: April 1, 2005. Laura M. Tarantino, Director, Office of Food Additive Safety, Center for Food Safety and Applied Nutrition. [FR Doc. 05–7727 Filed 4–15–05; 8:45 am] BILLING CODE 4160–01–S Frm 00045 Fmt 4703 Sfmt 4703 Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: PO 00000 Food and Drug Administration Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled ‘‘User Fee Waivers for FDC and Co-Packaged HIV Drugs for PEPFAR.’’ This draft guidance describes the circumstances under which certain applications for fixed dose combination (FDC) and copackaged versions of previously approved antiretroviral therapies for the treatment of human immunodeficiency virus (HIV) under the President’s Emergency Plan for Acquired Immunodeficiency Syndrome Relief (PEPFAR) will not be assessed user fees. The draft guidance also describes circumstances under which some of the applications that will be assessed fees may be eligible for a public health or a barrier-to-innovation waiver. DATES: Submit written or electronic comments on the draft guidance by June 17, 2005. General comments on agency guidance documents are welcome at any time. ADDRESSES: Submit written requests for single copies of the draft guidance to the Division of Drug Information (HFD– 240), Center for Drug Evaluation and Research, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857. Send one selfaddressed adhesive label to assist that office in processing your requests. Submit written comments on the draft guidance to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. Submit electronic comments to https:// www.fda.gov/dockets/ecomments. See the SUPPLEMENTARY INFORMATION section for electronic access to the draft guidance document. FOR FURTHER INFORMATION CONTACT: Michael Jones, Center for Drug Evaluation and Research (HFD–7), Food and Drug Administration, 5600 Fishers E:\FR\FM\18APN1.SGM 18APN1

Agencies

[Federal Register Volume 70, Number 73 (Monday, April 18, 2005)]
[Notices]
[Page 20145]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-7727]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2005F-0138]


Kareem I. Batarseh; Filing of Food Additive Petition

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that 
Kareem I. Batarseh has filed a petition proposing that the food 
additive regulations be amended to provide for the safe use of a 
mixture of hydrogen peroxide, silver nitrate, phosphoric acid, tartaric 
acid, glutamic acid, and sodium tripolyphosphate as an antimicrobial 
agent in bottled drinking water.

FOR FURTHER INFORMATION CONTACT: 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: Under the Federal Food, Drug, and Cosmetic 
Act (sec. 409 (b)(5) (21 U.S.C. 348(b)(5))), notice is given that a 
food additive petition (FAP 5A4759) has been filed by Kareem I. 
Batarseh, P.O. Box 8, College Park, MD 20741-0008. The petition 
proposes to amend the food additive regulations in part 172 Food 
Additives Permitted For Direct Addition To Food For Human Consumption 
(21 CFR part 172) to provide for the safe use of a mixture of hydrogen 
peroxide, silver nitrate, phosphoric acid, tartaric acid, glutamic 
acid, and sodium tripolyphosphate as an antimicrobial agent in bottled 
drinking water.
    The agency has determined under 21 CFR 25.32(k) 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.

    Dated: April 1, 2005.
Laura M. Tarantino,
Director, Office of Food Additive Safety, Center for Food Safety and 
Applied Nutrition.
[FR Doc. 05-7727 Filed 4-15-05; 8:45 am]
BILLING CODE 4160-01-S
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