United States Government Publishing Office publisher pbl distributor dst United States National Archives and Records Administration Office of the Federal Register author aut Government Organization text government publication eng FR Regulatory Information 1996_register executive 2010-09-24 article Part III Rules and Regulations D09002ee1be052337 D09002ee1be052477 United States Food Additives Permitted for Direct Addition to Food for Human originator org United States Government Agency or Subagency United States Department of Health and Human Services originator org United States Government Agency or Subagency United States Food and Drug Administration originator org United States Government Agency or Subagency The Food and Drug Administration (FDA) is amending the food additive regulations to provide for the safe use of sucrose esterified with medium and long chain fatty acids (olestra) as a replacement for fats and oils. This action is in response to a petition filed by the Procter & Gamble Co. 61 FR 3118 https://www.govinfo.gov/app/details/FR-1996-01-30/96-1584 96-1584 fr30ja96-21 4160-01-C Docket No. 87F-0179 https://www.govinfo.gov/app/details/FR-1996-01-30/96-1584 https://www.govinfo.gov/content/pkg/FR-1996-01-30/html/96-1584.htm https://www.govinfo.gov/content/pkg/FR-1996-01-30/pdf/96-1584.pdf 56 p. 3118 3173 61 FR 3118 Title 21 Part 172 21 CFR Part 172 Food Additives Permitted for Direct Addition to Food for Human Consumption; Olestra; Federal Register Vol. 61, Issue RULE 96-1584 III Food Additives Permitted for Direct Addition to Food for Human DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 1996-01-30 1996-04-01 1996-02-29 Docket No. 87F-0179 4160-01-C 96-1584 Final rule.

The Food and Drug Administration (FDA) is amending the food additive regulations to provide for the safe use of sucrose esterified with medium and long chain fatty acids (olestra) as a replacement for fats and oils. This action is in response to a petition filed by the Procter & Gamble Co.

The regulation is effective January 30, 1996. Submit written objections and requests for a hearing by February 29, 1996. Submit written comments on the labeling requirement (Sec. 172.867(c)) by April 1, 1996. The Director of the Office of the Federal Register approves the incorporations by reference in accordance with 5 U.S.C. 552(a) and 1 CFR part 51 of certain publications at 21 CFR 172.867, effective January 30, 1996. ADDRESSES: Submit written objections to the Dockets Management Branch (HFA-305), Food and Drug Administration, 12420 Parklawn Dr., rm. 1-23, Rockville, MD 20857. Helen R. Thorsheim, Center for Food Safety and Applied Nutrition (HFS-216), Food and Drug Administration, 200 C St. SW., Washington, DC 20204, 202-418-3092. Vol. 61, no. 20 Office of the Federal Register, National Archives and Records Administration 1996-01-30 continuing daily deposited born digital 294 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-1996-01-30 P0b002ee180a32dc5 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr30ja96 https://www.govinfo.gov/app/details/FR-1996-01-30 https://www.govinfo.gov/content/pkg/FR-1996-01-30/pdf/FR-1996-01-30.pdf fdlp 2891 3173 DGPO 2010-09-24 2023-05-07 FR-1996-01-30 machine generated eng FR FR-1996-01-30 61 20