Frozen Concentrate for Lemonade Deviating From Identity Standard; Temporary Permit for Market Testing, 11095 [E8-3912]

Download as PDF Federal Register / Vol. 73, No. 41 / Friday, February 29, 2008 / Notices components and systems within the DoD. The task force’s findings and recommendations, pursuant to 41 CFR 102–3.140 through 102–3.165, will be presented and discussed by the membership of the Defense Science Board prior to being presented to the Government’s decision maker. Pursuant to 41 CFR 102–3.120 and 102–3.150, the Designated Federal Officer for the Defense Science Board will determine and announce in the Federal Register when the findings and recommendations of the July 28–29, 2008 meeting are deliberated by the Defense Science Board. Interested persons may submit a written statement for consideration by the Defense Science Board. Individuals submitting a written statement must submit their statement to the Designated Federal Official at the address detailed below, at any point, however, if a written statement is not received at least 10 calendar days prior to the meeting, which is the subject of this notice, then it may not be provided to or considered by the Defense Science Board. The Designated Federal Official will review all timely submissions with the Defense Science Board Chairperson, and ensure they are provided to members of the Defense Science Board before the meeting that is the subject of this notice. FOR FURTHER INFORMATION CONTRACT: Major Charles Lominac, USAF, Defense Science Board, 3140 Defense Pentagon, Room 3B888A, Washington, DC 20301– 3140, via e-mail at charles.lominac@osd.mil, or via phone at (703) 571–0081. Dated: February 25, 2008. L.M. Bynum, Alternate OSD Federal Register, Liaison Officer, Department of Defense. [FR Doc. E8–3896 Filed 2–28–08; 8:45 am] BILLING CODE 5001–06–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2008–N–0131] Frozen Concentrate for Lemonade Deviating From Identity Standard; Temporary Permit for Market Testing AGENCY: Food and Drug Administration, rwilkins on PROD1PC63 with NOTICES HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is announcing that a temporary permit has been issued to Florida’s Natural Growers, to market VerDate Aug<31>2005 19:22 Feb 28, 2008 Jkt 214001 test a product designated as ‘‘Frozen Concentrate for Lemonade 3+1 Ratio’’ that deviates from the U.S. standard of identity for frozen concentrate for lemonade. The purpose of the temporary permit is to allow the applicant to measure customer acceptance of the product, identify mass production problems, and assess commercial feasibility. DATES: This permit is effective for 15 months, beginning on the date the permit holder introduces or causes the introduction of the test product into interstate commerce, but not later than May 29, 2008. FOR FURTHER INFORMATION CONTACT: Loretta A. Carey, Center for Food Safety and Applied Nutrition (HFS–820), Food and Drug Administration, 5100 Paint Branch Pkwy., College Park, MD 20740, 301–436–2371. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 130.17 concerning temporary permits to facilitate market testing of foods deviating from the requirements of the standards of identity issued under section 401 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 341), FDA is giving notice that a temporary permit has been issued to Florida’s Natural Growers, a division of Citrus World, Inc., 20205 U.S. Highway 27N, Lake Wales, Florida 33853. This permit covers limited interstate marketing tests of products identified as ‘‘Frozen Concentrate for Lemonade 3+1 Ratio’’ that deviate from the U.S. standard of identity for frozen concentrate for lemonade (21 CFR 146.120) in that the frozen concentrate for lemonade is a 3 + 1 fold dilution with a 56° Brix (measure of concentration of sugars in juice) rather than the 48° Brix as required in the standard. When diluted according to directions that appear on the label, the test product contains not less than 0.70 grams of acid per 100 milliliters and not less than 10.5 percent by weight of soluble solids. The test product meets all the requirements of the standard with the exception of the 3 + 1 fold dilution. The purpose of this temporary permit is to test the product throughout the United States, in order to allow the applicant to measure customer acceptance of the product, identify mass production problems, and assess commercial feasibility. This permit provides for the temporary marketing of a total of 20,000 cases per year of 12 x 32 ounce cartons (240,000 cartons). The total fluid quantity covered by this application is 227,100 liters (60,000 gallons). The test product will be manufactured at PO 00000 Frm 00008 Fmt 4703 Sfmt 4703 11095 Florida’s Natural Growers, a division of Citrus World, Inc., located at 20205 U.S. Highway 27N, Lake Wales, Florida 33853. Florida’s Natural Growers will distribute the test product throughout the United States. The information panel of the labels must bear nutrition labeling in accordance with 21 CFR 101.9. Each of the ingredients used in food must be declared on the label as required by the applicable sections of 21 CFR part 101. This permit is effective for 15 months, beginning on the date the permit holder introduces or causes the introduction of the product into interstate commerce, but not later than (see DATES). Dated: February 25, 2008. Barbara Schneeman, Director, Office of Nutritional Products, Labeling and Dietary Supplements, Center for Food Safety and Applied Nutrition. [FR Doc. E8–3912 Filed 2–28–08; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF DEFENSE Office of the Secretary [DOD–2008–OS–0013] Privacy Act of 1974; System of Records DoD; Defense Information Systems Agency. ACTION: Notice to Amend a System of Records. AGENCY: SUMMARY: Defense Information Systems Agency proposes to amend a system of records notice in its existing inventory of records systems subject to the Privacy Act of 1974, (5 U.S.C. 552a), as amended. This proposed action will be effective without further notice on March 31, 2008 unless comments are received which result in a contrary determination. DATES: Send comments to the Defense Information Systems Agency, 5600 Columbia Pike, Room 933–I, Falls Church, VA 22041–2705. FOR FURTHER INFORMATION CONTACT: Ms. Jeanette M. Weathers-Jenkins at (703) 681–2103. SUPPLEMENTARY INFORMATION: The Defense Information Systems Agency systems of records notices subject to the Privacy Act of 1974, (5 U.S.C. 552a), as amended, have been published in the Federal Register and are available from the address above. The specific changes to the record system being amended are set forth below followed by the notice, as ADDRESSES: E:\FR\FM\29FEN1.SGM 29FEN1

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[Federal Register Volume 73, Number 41 (Friday, February 29, 2008)]
[Notices]
[Page 11095]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-3912]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2008-N-0131]


Frozen Concentrate for Lemonade Deviating From Identity Standard; 
Temporary Permit for Market Testing

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
temporary permit has been issued to Florida's Natural Growers, to 
market test a product designated as ``Frozen Concentrate for Lemonade 
3+1 Ratio'' that deviates from the U.S. standard of identity for frozen 
concentrate for lemonade. The purpose of the temporary permit is to 
allow the applicant to measure customer acceptance of the product, 
identify mass production problems, and assess commercial feasibility.

DATES: This permit is effective for 15 months, beginning on the date 
the permit holder introduces or causes the introduction of the test 
product into interstate commerce, but not later than May 29, 2008.

FOR FURTHER INFORMATION CONTACT:  Loretta A. Carey, Center for Food 
Safety and Applied Nutrition (HFS-820), Food and Drug Administration, 
5100 Paint Branch Pkwy., College Park, MD 20740, 301-436-2371.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 130.17 concerning 
temporary permits to facilitate market testing of foods deviating from 
the requirements of the standards of identity issued under section 401 
of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 341), FDA is 
giving notice that a temporary permit has been issued to Florida's 
Natural Growers, a division of Citrus World, Inc., 20205 U.S. Highway 
27N, Lake Wales, Florida 33853.
    This permit covers limited interstate marketing tests of products 
identified as ``Frozen Concentrate for Lemonade 3+1 Ratio'' that 
deviate from the U.S. standard of identity for frozen concentrate for 
lemonade (21 CFR 146.120) in that the frozen concentrate for lemonade 
is a 3 + 1 fold dilution with a 56[deg] Brix (measure of concentration 
of sugars in juice) rather than the 48[deg] Brix as required in the 
standard. When diluted according to directions that appear on the 
label, the test product contains not less than 0.70 grams of acid per 
100 milliliters and not less than 10.5 percent by weight of soluble 
solids. The test product meets all the requirements of the standard 
with the exception of the 3 + 1 fold dilution. The purpose of this 
temporary permit is to test the product throughout the United States, 
in order to allow the applicant to measure customer acceptance of the 
product, identify mass production problems, and assess commercial 
feasibility.
    This permit provides for the temporary marketing of a total of 
20,000 cases per year of 12 x 32 ounce cartons (240,000 cartons). The 
total fluid quantity covered by this application is 227,100 liters 
(60,000 gallons). The test product will be manufactured at Florida's 
Natural Growers, a division of Citrus World, Inc., located at 20205 
U.S. Highway 27N, Lake Wales, Florida 33853. Florida's Natural Growers 
will distribute the test product throughout the United States. The 
information panel of the labels must bear nutrition labeling in 
accordance with 21 CFR 101.9. Each of the ingredients used in food must 
be declared on the label as required by the applicable sections of 21 
CFR part 101. This permit is effective for 15 months, beginning on the 
date the permit holder introduces or causes the introduction of the 
product into interstate commerce, but not later than (see DATES).

    Dated: February 25, 2008.
Barbara Schneeman,
Director, Office of Nutritional Products, Labeling and Dietary 
Supplements, Center for Food Safety and Applied Nutrition.
[FR Doc. E8-3912 Filed 2-28-08; 8:45 am]
BILLING CODE 4160-01-S
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