Food Additives Permitted in Feed and Drinking Water of Animals; Gamma-Linolenic Acid Safflower Meal, 35568-35570 [2015-15220]

Download as PDF 35568 Federal Register / Vol. 80, No. 119 / Monday, June 22, 2015 / Rules and Regulations DEPARTMENT OF TRANSPORTATION Rate (percent) IORR ....................... IOER ....................... Effective ⁄ ⁄ 12/18/2008 12/18/2008 14 14 Federal Aviation Administration tkelley on DSK3SPTVN1PROD with RULES (c) Pass-through balances. A passthrough correspondent that is an eligible institution may pass back to its respondent interest paid on balances maintained to satisfy a reserve balance requirement of that respondent. In the case of balances maintained by a passthrough correspondent that is not an eligible institution, a Reserve Bank may pay interest only on the balances maintained to satisfy a reserve balance requirement of one or more respondents up to the top of the penalty-free band, and the correspondent shall pass back to its respondents interest paid on balances in the correspondent’s account. (d) * * * (5) Interest on balances of eligible institutions maintained in an excess balance account is the amount equal to the IOER rate in effect each day multiplied by the total balances maintained on that day for each day of the maintenance period. * * * * * (f) Procedure for determination of rates. The Board anticipates that notice and public participation with respect to changes in the rate or rates of interest to be paid under this section will generally be impracticable, unnecessary, contrary to the public interest, or otherwise not required in the public interest, and that there will generally be reason and good cause in the public interest why the effective date should not be deferred for 30 days. The reason or reasons in such cases are generally expected to include that such notice, public participation, or deferment of effective date would prevent the action from becoming effective as promptly as necessary in the public interest, would permit speculators or others to reap unfair profits or to interfere with the Board’s actions taken with a view to accommodating commerce and business and with regard to their bearing upon the general credit situation of the country, would provoke other consequences contrary to the public interest, would not aid the persons affected, or would otherwise serve no useful purpose. By order of the Board of Governors of the Federal Reserve System, June 17, 2015. Robert deV. Frierson, Secretary of the Board. [FR Doc. 2015–15238 Filed 6–19–15; 8:45 am] BILLING CODE 6210–01–P VerDate Sep<11>2014 17:04 Jun 19, 2015 Jkt 235001 14 CFR Part 71 [Docket No. FAA–2015–0793; Airspace Docket No. 15–AEA–3] Amendment of Class D Airspace; Baltimore, Martin State Airport, MD Federal Aviation Administration (FAA), DOT. ACTION: Final rule, technical amendment; correction. AGENCY: This action corrects an error in the title of a final rule published in the Federal Register on April 29, 2015, amending Class D Airspace at Martin State Airport, Baltimore, MD. It should read Amendment of Class D Airspace Baltimore, Martin State Airport, MD. This action also corrects reference to Restricted Area R–4001C as being MSL, and corrects the airport designation. DATES: Effective 0901 UTC, June 25, 2015. The Director of the Federal Register approves this incorporation by reference action under title 1, Code of Federal Regulations, part 51, subject to the annual revision of FAA Order 7400.9 and publication of conforming amendments. SUMMARY: John Fornito, Operations Support Group, Eastern Service Center, Federal Aviation Administration, P.O. Box 20636, Atlanta, Georgia 30320; telephone (404) 305–6364. SUPPLEMENTARY INFORMATION: FOR FURTHER INFORMATION CONTACT: History On April 29, 2015, the FAA published a final rule, technical amendment in the Federal Register amending Class D airspace at Martin State Airport, Baltimore, MD. (80 FR 23709). After publication, the FAA found that the title was incorrectly typed as Proposed Amendment of Class E Airspace, Baltimore, MD, instead of Amendment of Class D Airspace, Baltimore, Martin State Airport, MD. This action makes the correction. Also, in the regulatory text, the airport designation is corrected to AEA D MD Baltimore, Martin State Airport, MD; and references to AGL is corrected to MSL. The Class D airspace designations are published in Paragraph 5000 of FAA Order 7400.9Y, dated August 9, 2014, and effective September 15, 2014, which is incorporated by reference in 14 CFR 71.1. The Class D airspace designation listed in this document will be published subsequently in the Order. PO 00000 Frm 00004 Fmt 4700 Sfmt 4700 Correction to Final Rule Accordingly, pursuant to the authority delegated to me, Docket No. FAA–2015–0793, amending Class D airspace at Martin State Airport, Baltimore, MD, as published in the Federal Register on April 29, 2015, (80 FR 23709), FR Doc. 2015–09870, is corrected as follows: On page 23709, column 1, line 39, remove, ‘‘Proposed Amendment of Class E Airspace; Baltimore, MD’’, and add in its place, ‘‘Amendment of Class D Airspace, Baltimore, Martin State Airport, MD’’, and on line 51 remove the abbreviation AGL and add in its place MSL. On page 23710, column 1, line 10, remove ‘‘ASO MD D Baltimore, MD [Amended]’’, and add in its place ‘‘AEA MD D Baltimore, Martin State Airport, MD [Amended]’’; and on line 27, remove the abbreviation AGL, and add in its place, MSL. Issued in College Park, Georgia, on June 10, 2015. Gerald E. Lynch, Acting Manager, Operations Support Group, Eastern Service Center, Air Traffic Organization. [FR Doc. 2015–15130 Filed 6–19–15; 8:45 am] BILLING CODE 4910–13–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 573 [Docket No. FDA–2010–F–0537] Food Additives Permitted in Feed and Drinking Water of Animals; GammaLinolenic Acid Safflower Meal AGENCY: Food and Drug Administration, HHS. ACTION: Final rule. The Food and Drug Administration (FDA or the Agency) is amending the regulations for food additives permitted in feed and drinking water of animals to provide for the safe use of seed meal from a variety of bioengineered safflower in cattle and poultry feeds. This action is in response to a food additive petition filed by Arcadia Biosciences, Inc. DATES: This rule is effective June 22, 2015. Submit either written or electronic objections and requests for a hearing by July 22, 2015. See section V of this document for information on the filing of objections. ADDRESSES: You may submit either electronic or written objections and a request for a hearing, identified by SUMMARY: E:\FR\FM\22JNR1.SGM 22JNR1 Federal Register / Vol. 80, No. 119 / Monday, June 22, 2015 / Rules and Regulations Docket No. FDA–2010–F–0537, by any of the following methods: Electronic Submissions Submit electronic objections in the following way: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the instructions for submitting comments. tkelley on DSK3SPTVN1PROD with RULES Written Submissions Submit written objections in the following ways: • Mail/Hand delivery/Courier (for paper 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 number for this rulemaking. All objections received will be posted without change to https:// www.regulations.gov, including any personal information provided. For additional information on submitting objections, see the ‘‘Objections’’ heading of the SUPPLEMENTARY INFORMATION section of this document. Docket: For access to the docket to read background documents or objections received, go to https:// www.regulations.gov and insert the docket number, 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: Isabel W. Pocurull, Center for Veterinary Medicine (HFV–226), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240–402–5877, isabel.pocurull@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background In a notice published in the Federal Register of October 20, 2010 (75 FR 64733), FDA announced that a food additive petition (animal use) (FAP 2267) had been filed by Arcadia Biosciences, Inc., 202 Cousteau Pl., suite 105, Davis, CA 95618. The petition proposed to amend the food additive regulations to provide for the safe use of seed meal from a variety of bioengineered safflower (Carthamus tinctorius L.) in cattle and poultry feeds. The safflower variety has been bioengineered to contain a gene from the water mold Saprolegnia diclina responsible for production of gammalinolenic acid in the seed oil. Seed meals are the ground residues obtained after processing seeds to extract their oil and are a common ingredient in livestock feed. The notice of filing VerDate Sep<11>2014 17:04 Jun 19, 2015 Jkt 235001 provided for a 30-day comment period on the petitioner’s environmental assessment. II. Conclusion FDA concludes that the data establish the safety and utility of gamma-linolenic acid safflower meal for use as proposed and that the food additive regulations should be amended as set forth in this document. III. Public Disclosure In accordance with § 571.1(h) (21 CFR 571.1(h)), the petition and documents we considered and relied upon in reaching our decision to approve the petition will be made available for public disclosure (see FOR FURTHER INFORMATION CONTACT). As provided in § 571.1(h), we will delete from the documents any materials that are not available for public disclosure. IV. Environmental Impact The Agency has carefully considered the potential environmental impact of this action and has concluded that the action will not have a significant impact on the human environment and that an environmental impact statement is not required. FDA’s finding of no significant impact and the evidence supporting that finding, contained in an environmental assessment, may be seen in the Division of Dockets Management (address above) between 9 a.m. and 4 p.m., Monday through Friday. V. Objections and Hearing Requests Any person who will be adversely affected by this regulation may file with the Division of Dockets Management (see ADDRESSES) either electronic or written objections. Each objection shall be separately numbered, and each numbered objection shall specify with particularity the provision of the regulation to which objection is made and the grounds for the objection. Each numbered objection on which a hearing is requested shall specifically so state. Failure to request a hearing for any particular objection shall constitute a waiver of the right to a hearing on that objection. Each numbered objection for which a hearing is requested shall include a detailed description and analysis of the specific factual information intended to be presented in support of the objection in the event that a hearing is held. Failure to include such a description and analysis for any particular objection shall constitute a waiver of the right to a hearing on the objection. It is only necessary to send one set of documents. Identify documents with the docket number found in brackets in the PO 00000 Frm 00005 Fmt 4700 Sfmt 4700 35569 heading of this document. Any objections received in response to the regulation may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday, and will be posted to the docket at https:// www.regulations.gov. List of Subjects in 21 CFR Part 573 Animal feeds, Food additives. Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs and redelegated to the Center for Veterinary Medicine, 21 CFR part 573 is amended as follows: PART 573—FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS 1. The authority citation for 21 CFR part 573 continues to read as follows: ■ Authority: 21 U.S.C. 321, 342, 348. ■ 2. Add § 573.490 to read as follows: § 573.490 meal. Gamma-linolenic acid safflower The food additive consists of the meal obtained after the removal of most of the oil from whole seeds or partially dehulled seeds or both obtained from a Carthamus tinctorius L. safflower Centennial variety genetically engineered to express the delta-6desaturase gene from Saprolegnia diclina Humphrey. The 453 amino acid, delta-6-desaturase enzyme converts the fatty acid linoleic acid to gammalinolenic acid during seed development. The resulting additive may be safely used in cattle and poultry feeds in accordance with the following prescribed conditions: (a) The additive shall contain not less than 20 percent crude protein, not more than 40 percent crude fiber, not more than 10 percent moisture, and not more than 2 percent crude fat. (b) The crude fat in the additive meets the following specifications: (1) Gamma-linolenic acid content not to exceed 55 percent. (2) Total content of stearidonic acid and cis, cis-6, 9-octadecadienoic acid not to exceed a total of 0.5 percent. (3) Total content of palmitic, stearic, oleic, linoleic, and other associated fatty acids to exceed a total of 40 percent. (c) The additive is used or intended for use in cattle and poultry feeds as a source of protein in accordance with good manufacturing and feeding practices. (d) To assure safe use of the additive, in addition to the other information required by the Food, Drug, and Cosmetic Act, the label and labeling of E:\FR\FM\22JNR1.SGM 22JNR1 35570 Federal Register / Vol. 80, No. 119 / Monday, June 22, 2015 / Rules and Regulations the additive, any feed premix, or complete feed shall bear the following: (1) The name of the additive or the common name, safflower meal. (2) Adequate directions for use in cattle and poultry feeds. (e) The additive may be identified by the common or usual name, safflower meal. Dated: June 16, 2015. Bernadette Dunham, Director, Center for Veterinary Medicine. [FR Doc. 2015–15220 Filed 6–19–15; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HOMELAND SECURITY Coast Guard 33 CFR Part 117 [Docket No. USCG–2015–0569] Drawbridge Operation Regulation; Willamette River, Portland, OR Coast Guard, DHS. Notice of deviation from drawbridge regulation. AGENCY: ACTION: The Coast Guard has issued a temporary deviation from the operating schedule that governs the Morrison Bridge, mile 12.8, and the Hawthorne Bridge, mile 13.1, both crossing the Willamette River at Portland, OR. The deviation is necessary to accommodate Portland’s Red, White, and Blues Run/ Walk event. The deviation allows the bridges to remain in the closed-tonavigation position from 5 a.m. to 10 a.m. on July 5, 2015 to allow for the safe movement of event participants across the bridges. DATES: This deviation is effective from 5 a.m. to 10 a.m. on July 5, 2015. ADDRESSES: The docket for this deviation, [USCG–2015–0569] is available at https://www.regulations.gov. Type the docket number in the ‘‘SEARCH’’ box and click ‘‘SEARCH.’’ Click on Open Docket Folder on the line associated with this deviation. You may also visit the Docket Management Facility in Room W12–140 on the ground floor of the Department of Transportation West Building, 1200 New Jersey Avenue SE., Washington, DC 20590, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. FOR FURTHER INFORMATION CONTACT: If you have questions on this temporary deviation, call or email Mr. Steven Fischer, Bridge Administrator, Thirteenth Coast Guard District; tkelley on DSK3SPTVN1PROD with RULES SUMMARY: VerDate Sep<11>2014 17:04 Jun 19, 2015 Jkt 235001 telephone 206–220–7282, email d13-pfd13bridges@uscg.mil. If you have questions on viewing the docket, call Cheryl Collins, Program Manager, Docket Operations, telephone 202–366– 9826. DEPARTMENT OF HOMELAND SECURITY SUPPLEMENTARY INFORMATION: [Docket No. USCG–2015–0488] Multnomah County has requested that the Hawthorne and Morrison drawbridges across the Willamette River in Portland, OR remain closed to vessel traffic from 5 a.m. to 10 a.m. on July 5, 2015 to facilitate safe, uninterrupted roadway passage of event participants for the Red, White and Blues Run/Walk event. The Morrison Bridge, mile 12.8, provides a vertical clearance of 69 feet in the closed position, and the Hawthorne Bridge, mile 13.1, provides 49 feet of vertical clearance in the closed position, all clearances are referenced to the vertical clearance above Columbia River Datum 0.0. This deviation allows the Hawthorne and Morrison Bridges, across the Willamette River, to remain in the closed position and need not open for maritime traffic from 5 a.m. to 10 a.m. on July 5, 2015. Waterway usage on this part of the Willamette River includes vessels ranging from commercial tug and barge to small pleasure craft. Vessels able to pass through the bridges in the closed positions may do so at any time. The bridges will be able to open for emergencies and there is no immediate alternate route for vessels to pass. The Coast Guard will also inform the users of the waterways through our Local and Broadcast Notices to Mariners of the change in operating schedule for the bridges so that vessels can arrange their transits to minimize any impact caused by the temporary deviation. In accordance with 33 CFR 117.35(e), the drawbridge must return to its regular operating schedule immediately at the end of the designated time period. This deviation from the operating regulations is authorized under 33 CFR 117.35. Dated: June 17, 2015. Steven M. Fischer, Bridge Administrator, Thirteenth Coast Guard District. [FR Doc. 2015–15215 Filed 6–19–15; 8:45 am] BILLING CODE 9110–04–P PO 00000 Frm 00006 Fmt 4700 Sfmt 4700 Coast Guard 33 CFR Part 165 Safety Zone; Southern California Annual Fireworks Events for the San Diego Captain of the Port Zone Coast Guard, DHS. Notice of enforcement of regulation. AGENCY: ACTION: The Coast Guard will enforce a safety zone on the waters of San Diego Bay, California, adjacent to the Embarcadero Marina Park South, for the annual San Diego Symphony Summer Pops Fireworks shows held on specific evenings from June 27, 2015 to September 6, 2015. The brief fireworks displays are scheduled to coincide with the end of the symphony concerts. This action is necessary to provide for safety of the marine event crew, spectators, safety vessels, and general users of the waterway. During the enforcement period, persons and vessels are prohibited from entering into, transiting through, or anchoring within this regulated area unless authorized by the Captain of the Port, or his designated representative. DATES: The regulations for the safety zone listed in 33 CFR 165.1123, Table 1, Item 1, will be enforced on various dates between June 27, 2015 to September 6, 2015, from 9 p.m. to 10 p.m. FOR FURTHER INFORMATION CONTACT: If you have questions on this publication, call or email Petty Officer Randolph Pahilanga, Waterways Management, U.S. Coast Guard Sector San Diego, CA; telephone (619) 278–7656, email D11PF-MarineEventsSanDiego@uscg.mil. SUPPLEMENTARY INFORMATION: The Coast Guard will enforce a safety zone in San Diego Bay, California, for the annual San Diego Symphony Summer Pops concerts (Item 1 on Table 1 of 33 CFR 165.1123), held on from 9 p.m. to 10 p.m. on various dates. Specifically, the dates of enforcement are: June 27, July 3, July 5, July 17, July 18, July 24, July 25, July 31, August 1, August 7, August 8, August 14, August 15, August 21, August 22, August 28, August 29, and September 4 through September 6, 2015. The safety zone is located off of the Embarcadero Marina Park South. Under the provisions of 33 CFR 165.1123, persons and vessels are prohibited during the fireworks display times from entering into, transiting SUMMARY: E:\FR\FM\22JNR1.SGM 22JNR1

Agencies

[Federal Register Volume 80, Number 119 (Monday, June 22, 2015)]
[Rules and Regulations]
[Pages 35568-35570]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-15220]


=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 573

[Docket No. FDA-2010-F-0537]


Food Additives Permitted in Feed and Drinking Water of Animals; 
Gamma-Linolenic Acid Safflower Meal

AGENCY: Food and Drug Administration, HHS.

ACTION: Final rule.

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

SUMMARY: The Food and Drug Administration (FDA or the Agency) is 
amending the regulations for food additives permitted in feed and 
drinking water of animals to provide for the safe use of seed meal from 
a variety of bioengineered safflower in cattle and poultry feeds. This 
action is in response to a food additive petition filed by Arcadia 
Biosciences, Inc.

DATES: This rule is effective June 22, 2015. Submit either written or 
electronic objections and requests for a hearing by July 22, 2015. See 
section V of this document for information on the filing of objections.

ADDRESSES: You may submit either electronic or written objections and a 
request for a hearing, identified by

[[Page 35569]]

Docket No. FDA-2010-F-0537, by any of the following methods:

Electronic Submissions

    Submit electronic objections in the following way:
     Federal eRulemaking Portal: https://www.regulations.gov. 
Follow the instructions for submitting comments.

Written Submissions

    Submit written objections in the following ways:
     Mail/Hand delivery/Courier (for paper 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 number for this rulemaking. All objections received will be 
posted without change to https://www.regulations.gov, including any 
personal information provided. For additional information on submitting 
objections, see the ``Objections'' heading of the SUPPLEMENTARY 
INFORMATION section of this document.
    Docket: For access to the docket to read background documents or 
objections received, go to https://www.regulations.gov and insert the 
docket number, 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: Isabel W. Pocurull, Center for 
Veterinary Medicine (HFV-226), Food and Drug Administration, 7519 
Standish Pl., Rockville, MD 20855, 240-402-5877, 
isabel.pocurull@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: 

I. Background

    In a notice published in the Federal Register of October 20, 2010 
(75 FR 64733), FDA announced that a food additive petition (animal use) 
(FAP 2267) had been filed by Arcadia Biosciences, Inc., 202 Cousteau 
Pl., suite 105, Davis, CA 95618. The petition proposed to amend the 
food additive regulations to provide for the safe use of seed meal from 
a variety of bioengineered safflower (Carthamus tinctorius L.) in 
cattle and poultry feeds. The safflower variety has been bioengineered 
to contain a gene from the water mold Saprolegnia diclina responsible 
for production of gamma-linolenic acid in the seed oil. Seed meals are 
the ground residues obtained after processing seeds to extract their 
oil and are a common ingredient in livestock feed. The notice of filing 
provided for a 30-day comment period on the petitioner's environmental 
assessment.

II. Conclusion

    FDA concludes that the data establish the safety and utility of 
gamma-linolenic acid safflower meal for use as proposed and that the 
food additive regulations should be amended as set forth in this 
document.

III. Public Disclosure

    In accordance with Sec.  571.1(h) (21 CFR 571.1(h)), the petition 
and documents we considered and relied upon in reaching our decision to 
approve the petition will be made available for public disclosure (see 
FOR FURTHER INFORMATION CONTACT). As provided in Sec.  571.1(h), we 
will delete from the documents any materials that are not available for 
public disclosure.

IV. Environmental Impact

    The Agency has carefully considered the potential environmental 
impact of this action and has concluded that the action will not have a 
significant impact on the human environment and that an environmental 
impact statement is not required. FDA's finding of no significant 
impact and the evidence supporting that finding, contained in an 
environmental assessment, may be seen in the Division of Dockets 
Management (address above) between 9 a.m. and 4 p.m., Monday through 
Friday.

V. Objections and Hearing Requests

    Any person who will be adversely affected by this regulation may 
file with the Division of Dockets Management (see ADDRESSES) either 
electronic or written objections. Each objection shall be separately 
numbered, and each numbered objection shall specify with particularity 
the provision of the regulation to which objection is made and the 
grounds for the objection. Each numbered objection on which a hearing 
is requested shall specifically so state. Failure to request a hearing 
for any particular objection shall constitute a waiver of the right to 
a hearing on that objection. Each numbered objection for which a 
hearing is requested shall include a detailed description and analysis 
of the specific factual information intended to be presented in support 
of the objection in the event that a hearing is held. Failure to 
include such a description and analysis for any particular objection 
shall constitute a waiver of the right to a hearing on the objection.
    It is only necessary to send one set of documents. Identify 
documents with the docket number found in brackets in the heading of 
this document. Any objections received in response to the regulation 
may be seen in the Division of Dockets Management between 9 a.m. and 4 
p.m., Monday through Friday, and will be posted to the docket at https://www.regulations.gov.

List of Subjects in 21 CFR Part 573

    Animal feeds, Food additives.

    Therefore, under the Federal Food, Drug, and Cosmetic Act and under 
authority delegated to the Commissioner of Food and Drugs and 
redelegated to the Center for Veterinary Medicine, 21 CFR part 573 is 
amended as follows:

PART 573--FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF 
ANIMALS

0
1. The authority citation for 21 CFR part 573 continues to read as 
follows:

    Authority:  21 U.S.C. 321, 342, 348.


0
2. Add Sec.  573.490 to read as follows:


Sec.  573.490  Gamma-linolenic acid safflower meal.

    The food additive consists of the meal obtained after the removal 
of most of the oil from whole seeds or partially dehulled seeds or both 
obtained from a Carthamus tinctorius L. safflower Centennial variety 
genetically engineered to express the delta-6-desaturase gene from 
Saprolegnia diclina Humphrey. The 453 amino acid, delta-6-desaturase 
enzyme converts the fatty acid linoleic acid to gamma-linolenic acid 
during seed development. The resulting additive may be safely used in 
cattle and poultry feeds in accordance with the following prescribed 
conditions:
    (a) The additive shall contain not less than 20 percent crude 
protein, not more than 40 percent crude fiber, not more than 10 percent 
moisture, and not more than 2 percent crude fat.
    (b) The crude fat in the additive meets the following 
specifications:
    (1) Gamma-linolenic acid content not to exceed 55 percent.
    (2) Total content of stearidonic acid and cis, cis-6, 9-
octadecadienoic acid not to exceed a total of 0.5 percent.
    (3) Total content of palmitic, stearic, oleic, linoleic, and other 
associated fatty acids to exceed a total of 40 percent.
    (c) The additive is used or intended for use in cattle and poultry 
feeds as a source of protein in accordance with good manufacturing and 
feeding practices.
    (d) To assure safe use of the additive, in addition to the other 
information required by the Food, Drug, and Cosmetic Act, the label and 
labeling of

[[Page 35570]]

the additive, any feed premix, or complete feed shall bear the 
following:
    (1) The name of the additive or the common name, safflower meal.
    (2) Adequate directions for use in cattle and poultry feeds.
    (e) The additive may be identified by the common or usual name, 
safflower meal.

    Dated: June 16, 2015.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. 2015-15220 Filed 6-19-15; 8:45 am]
 BILLING CODE 4164-01-P

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