21 CFR Part 172 - FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION | Title 21 - Food and Drugs | Code of Federal Regulations

Authority:

21 U.S.C. 321, 341, 342, 348, 371, 379e.

Source:

42 FR 14491, Mar. 15, 1977, unless otherwise noted.

Editorial Note:

Nomenclature changes to part 172 appear at 61 FR 14482, Apr. 2, 1996, 66 FR 56035, Nov. 6, 2001, 66 FR 66742, Dec. 27, 2001, 68 FR 15355, Mar. 31, 2003, 70 FR 40880, July 15, 2005, 70 FR 67651, Nov. 8, 2005, and 70 FR 72074, Dec. 1, 2005.

Title 21 published on 2012-04-01

The following are only the Rules published in the Federal Register after the published date of Title 21.

For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.

2013-03-07; vol. 78 # 45 - Thursday, March 7, 2013

78 FR 14664 - Food and Color Additives; Technical Amendments

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2013-04701
RIN
Docket No.	FDA-2012-N-0010

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule; technical amendments.

This rule is effective March 7, 2013.

21 CFR Parts 73, 172, 173, 176, 177, 178, 184, and 189

Summary

The Food and Drug Administration (FDA) is amending certain regulations regarding food and color additives to correct minor errors (such as misspelled chemical names) and to update office names and addresses. This action is editorial in nature and is intended to improve the accuracy of the Agency's regulations.

2012-08-29; vol. 77 # 168 - Wednesday, August 29, 2012

77 FR 52228 - Food Additives Permitted for Direct Addition to Food for Human Consumption; Vitamin D 2 Bakers Yeast

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-21353
RIN
Docket No.	FDA-2009-F-0570

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule.

This rule is effective August 29, 2012. Submit either electronic or written objections and requests for a hearing by September 28, 2012. See section VII of this document for information on filing objections.

21 CFR Part 172

Summary

The Food and Drug Administration (FDA) is amending the food additive regulations to provide for the safe use of vitamin D 2 bakers yeast as a source of vitamin D 2 and as a leavening agent in yeast-leavened baked products at levels not to exceed 400 International Units (IU) of vitamin D 2 per 100 grams (g) in the finished food. This action is in response to a petition filed by Lallemand, Inc. (Lallemand).

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.

Title 21 published on 2012-04-01

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 172 after this date.

2013-03-07; vol. 78 # 45 - Thursday, March 7, 2013

78 FR 14664 - Food and Color Additives; Technical Amendments

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2013-04701
RIN
Docket No.	FDA-2012-N-0010

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule; technical amendments.

This rule is effective March 7, 2013.

21 CFR Parts 73, 172, 173, 176, 177, 178, 184, and 189

Summary

The Food and Drug Administration (FDA) is amending certain regulations regarding food and color additives to correct minor errors (such as misspelled chemical names) and to update office names and addresses. This action is editorial in nature and is intended to improve the accuracy of the Agency's regulations.

2012-10-26; vol. 77 # 208 - Friday, October 26, 2012

77 FR 65340 - Ajinomoto Co., Inc.; Filing of Food Additive Petition; Amendment

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-26315
RIN
Docket No.	FDA-2009-F-0303

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petition.

Submit either electronic or written comments on the petitioner's environmental assessment by November 26, 2012.

21 CFR Part 172

Summary

The Food and Drug Administration (FDA) is amending the filing notice for a food additive petition filed by Ajinomoto Co., Inc., to indicate that the petitioned additive, N-[N-[3-(3-hydroxy-4-methoxyphenyl) propyl-α-aspartyl]-L-phenylalanine 1-methyl ester, monohydrate (proposed additive name Advantame, CAS Reg. No. 714229-20-6), is for use as a non-nutritive sweetener and flavor enhancer in foods generally, except meat and poultry. The previous filing notice indicated that the proposed additive was for use as a non-nutritive sweetener in tabletop applications and powdered beverage mixes.

2012-09-04; vol. 77 # 171 - Tuesday, September 4, 2012

77 FR 53801 - Nexira; Filing of Food Additive Petition; Amendment

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-21639
RIN
Docket No.	FDA-2011-F-0765

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petition.

Submit either electronic or written comments on the petitioner's environmental assessment by October 4, 2012.

21 CFR Part 172

Summary

The Food and Drug Administration (FDA) is amending the filing notice for a food additive petition filed by Nexira proposing that the food additive regulations be amended to provide for the expanded safe use of acacia gum (gum arabic) in foods.

2012-08-29; vol. 77 # 168 - Wednesday, August 29, 2012

77 FR 52228 - Food Additives Permitted for Direct Addition to Food for Human Consumption; Vitamin D 2 Bakers Yeast

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-21353
RIN
Docket No.	FDA-2009-F-0570

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule.

This rule is effective August 29, 2012. Submit either electronic or written objections and requests for a hearing by September 28, 2012. See section VII of this document for information on filing objections.

21 CFR Part 172

Summary

The Food and Drug Administration (FDA) is amending the food additive regulations to provide for the safe use of vitamin D 2 bakers yeast as a source of vitamin D 2 and as a leavening agent in yeast-leavened baked products at levels not to exceed 400 International Units (IU) of vitamin D 2 per 100 grams (g) in the finished food. This action is in response to a petition filed by Lallemand, Inc. (Lallemand).

2012-07-18; vol. 77 # 138 - Wednesday, July 18, 2012

77 FR 42229 - Gruma Corporation, Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza; Filing of Food Additive Petition; Correction

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-17432
RIN
Docket No.	FDA-2012-F-0480

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petition; correction.

21 CFR Part 172

Summary

The Food and drug Administration (FDA) is correcting a notice that appeared in the Federal Register of June 13, 2012 (77 FR 35317). The document announced that Gruma Corporation, Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza had jointly filed a petition proposing that the food additive regulations be amended to provide for the safe use of folic acid in corn masa flour. The document was published with an error in the title of the document signer's signature. This document corrects that error.

2012-06-13; vol. 77 # 114 - Wednesday, June 13, 2012

77 FR 35317 - Gruma Corporation, Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza; Filing of Food Additive Petition

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-14263
RIN
Docket No.	FDA-2012-F-0480

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petition.

21 CFR Part 172

Summary

The Food and Drug Administration (FDA) is announcing that Gruma Corporation, Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza have jointly filed a petition proposing that the food additive regulations be amended to provide for the safe use of folic acid in corn masa flour.

21 CFR Part 172 - FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION

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