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Rule

Code of Federal Regulations; Technical Amendments

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Information about this document as published in the Federal Register.

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AGENCY:

Food and Drug Administration, HHS.

ACTION:

Final rule; technical amendments.

SUMMARY:

The Food and Drug Administration (FDA) is amending its regulations to reflect a correct footnote and a part heading. This action is being taken to improve the accuracy of the regulations.

EFFECTIVE DATE:

April 10, 2000.

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FOR FURTHER INFORMATION CONTACT:

LaJuana D. Caldwell, Office of Policy, Planning, and Legislation (HF-27), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857.

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SUPPLEMENTARY INFORMATION:

FDA has discovered that errors have been incorporated into the agency's codified regulations for 21 CFR parts 211 and 720. This document corrects those errors. Publication of this document constitutes final action under the Administrative Procedure Act (5 U.S.C. 553). FDA has determined that notice and public comment are unnecessary because this amendment is nonsubstantive.

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List of Subjects

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Therefore, under the Federal Food, Drug, and Cosmetic Act and under authority delegated to the Commissioner of Food and Drugs,

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PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

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1. The authority citation for

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Authority: 21 U.S.C. 321, 351, 352, 355, 360b, 371, 374.

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[Amended]
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2. Section 211.194

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PART 720—VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS

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3. The authority citation for

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Authority: 21 U.S.C. 321, 331, 361, 362, 371, 374.

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4. The heading for part 720 is revised to read as set forth above.

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Dated: March 31, 2000.

Margaret M. Dotzel,

Acting Associate Commissioner for Policy.

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[FR Doc. 00-8716 Filed 4-7-00; 8:45 am]

BILLING CODE 4160-01-F