21 CFR 73 - LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION

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Authority: 21 U.S.C. 321, 341, 342, 343, 348, 351, 352, 355, 361, 362, 371, 379e.

Source: 42 FR 15643, Mar. 22, 1977, unless otherwise noted.

Title 21 published on 2011-04-01

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.

2011-09-27; vol. 76 # 187 - Tuesday, September 27, 2011

76 FR 59503 - Listing of Color Additives Exempt From Certification; Reactive Blue 69; Confirmation of Effective Date

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2011-24795
RIN
Docket No.	FDA-2009-C-0543

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule; confirmation of effective date.

The effective date confirmed: June 6, 2011.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is confirming the effective date of June 6, 2011, for the final rule that appeared in the Federal Register of May 4, 2011 (76 FR 25234). The final rule amended the color additive regulations to provide for the safe use of disodium 1-amino-4-[[4-[(2-bromo-1-oxoallyl)amino]-2-sulphonatophenyl]amino]-9,10-dihydro-9,10-dioxoanthracene-2-sulphonate (CAS Reg. No. 70209-99-3), also known as Reactive Blue 69, as a color additive in contact lenses.

2011-05-04; vol. 76 # 86 - Wednesday, May 4, 2011

76 FR 25234 - Listing of Color Additives Exempt From Certification; Reactive Blue 69

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2011-10869
RIN
Docket No.	FDA-2009-C-0543

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule.

This rule is effective June 6, 2011. Submit either electronic or written objections and requests for a hearing by June 3, 2011. See section VII of this document for information on the filing of objections.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is amending the color additive regulations to provide for the safe use of disodium 1-amino-4-[[4-[(2-bromo-1-oxoallyl)amino]-2-sulphonatophenyl]amino]-9,10-dihydro-9,10-dioxoanthracene-2-sulphonate (CAS Reg. No. 70209-99-3), also known as Reactive Blue 69, as a color additive in contact lenses. This action is in response to a petition filed by Sauflon Pharmaceuticals Ltd.

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.

United States Code

21 USC 321 - Definitions; generally

21 USC 341 - Definitions and standards for food

21 USC 342 - Adulterated food

21 USC 343 - Misbranded food

21 USC 348 - Food additives

21 USC 351 - Adulterated drugs and devices

21 USC 352 - Misbranded drugs and devices

21 USC 355 - New drugs

21 USC 361 - Adulterated cosmetics

21 USC 362 - Misbranded cosmetics

21 USC 379e - Listing and certification of color additives for foods, drugs, devices, and cosmetics

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 73

2012-03-22; vol. 77 # 56 - Thursday, March 22, 2012

77 FR 16784 - E. & J. Gallo Winery; Filing of Color Additive Petition

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-6854
RIN
Docket No.	FDA-2012-C-0224

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petition.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is announcing that E. & J. Gallo Winery has filed a petition proposing that the color additive regulations be amended to provide for the expanded safe use of mica-based pearlescent pigments as color additives in certain distilled spirits.

2012-01-20; vol. 77 # 13 - Friday, January 20, 2012

77 FR 2935 - Mars, Inc.; Filing of Color Additive Petition

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2012-599
RIN
Docket No.	FDA-2011-C-0878

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petition.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is announcing that Mars, Inc., has filed a petition proposing that the color additive regulations be amended to provide for the safe use of spirulina blue, an extract made from the biomass of Anthrospira platensis (spirulina), to color candy and chewing gum.

2011-09-27; vol. 76 # 187 - Tuesday, September 27, 2011

76 FR 59503 - Listing of Color Additives Exempt From Certification; Reactive Blue 69; Confirmation of Effective Date

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2011-24795
RIN
Docket No.	FDA-2009-C-0543

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule; confirmation of effective date.

The effective date confirmed: June 6, 2011.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is confirming the effective date of June 6, 2011, for the final rule that appeared in the Federal Register of May 4, 2011 (76 FR 25234). The final rule amended the color additive regulations to provide for the safe use of disodium 1-amino-4-[[4-[(2-bromo-1-oxoallyl)amino]-2-sulphonatophenyl]amino]-9,10-dihydro-9,10-dioxoanthracene-2-sulphonate (CAS Reg. No. 70209-99-3), also known as Reactive Blue 69, as a color additive in contact lenses.

2011-09-07; vol. 76 # 173 - Wednesday, September 7, 2011

76 FR - CooperVision, Inc.; Filing of Color Additive Petitions

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	C2-2011-16089
RIN
Docket No.	s. FDA-2011-C-0344 and FDA-2011-C-0463

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

21 CFR Part 73

Summary

2011-08-11; vol. 76 # 155 - Thursday, August 11, 2011

76 FR 49707 - CooperVision, Inc.; Filing of Color Additive Petitions

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	C1-2011-16089
RIN
Docket No.	s. FDA-2011-C-0344 and FDA-2011-C-0463

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

21 CFR Part 73

Summary

2011-06-28; vol. 76 # 124 - Tuesday, June 28, 2011

76 FR 37690 - CooperVision, Inc.; Filing of Color Additive Petitions

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2011-16089
RIN
Docket No.	s. FDA-2011-C-0344 and FDA-2011-C-0463

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Notice of petitions.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is announcing that CooperVision, Inc., has filed two petitions proposing that the color additive regulations be amended to provide for the safe use of 1,4-bis[4-(2-methacryloxyethyl)phenlyamino] anthraquinone (C.I. Reactive Blue 246) and 1,4-bis[(2-hydroxyethyl)amino]-9,10-anthracenedione bis(2-methyl-2-propenoic)ester (C.I. Reactive Blue 247). The color additives are intended to be copolymerized with various monomers for use as colored contact lens materials.

2011-05-04; vol. 76 # 86 - Wednesday, May 4, 2011

76 FR 25234 - Listing of Color Additives Exempt From Certification; Reactive Blue 69

GPO FDSys XML | Text

Additional Documents

type	regulations.gov
FR Doc.	2011-10869
RIN
Docket No.	FDA-2009-C-0543

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration

Final rule.

This rule is effective June 6, 2011. Submit either electronic or written objections and requests for a hearing by June 3, 2011. See section VII of this document for information on the filing of objections.

21 CFR Part 73

Summary

The Food and Drug Administration (FDA) is amending the color additive regulations to provide for the safe use of disodium 1-amino-4-[[4-[(2-bromo-1-oxoallyl)amino]-2-sulphonatophenyl]amino]-9,10-dihydro-9,10-dioxoanthracene-2-sulphonate (CAS Reg. No. 70209-99-3), also known as Reactive Blue 69, as a color additive in contact lenses. This action is in response to a petition filed by Sauflon Pharmaceuticals Ltd.

21 CFR 73 - LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION

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