[Federal Register Volume 60, Number 17 (Thursday, January 26, 1995)]
[Rules and Regulations]
[Page 5131]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-2005]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 74 and 201
[Docket No. 92C-0293]
Listing of Color Additives Subject to Certification; FD&C Yellow
No. 5; Confirmation of Effective Date
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; confirmation of effective date.
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SUMMARY: The Food and Drug Administration (FDA) is confirming the
effective date of December 30, 1994, of the final rule that appeared in
the Federal Register of November 29, 1994 (59 FR 60893) (effective date
corrected in the Federal Register of December 2, 1994 ( 59 FR 61929)),
and amended the color additive regulations to provide for the safe use
of FD&C Yellow No. 5 and FD&C Yellow No. 5 Aluminum Lake for coloring
drugs and cosmetics intended for use in the area of the eye.
DATES: Effective date confirmed: December 30, 1994.
FOR FURTHER INFORMATION CONTACT: Robert L. Martin, Center for Food
Safety and Applied Nutrition (HFS-217), Food and Drug Administration,
200 C St. SW., Washington, DC 20204-0001, 202-418-3074.
SUPPLEMENTARY INFORMATION: In the Federal Register of November 29, 1994
(59 FR 60893) (effective date corrected in the Federal Register of
December 2, 1994 (59 FR 61929)), FDA amended 21 CFR 74.1705 and 74.2705
to provide for the safe use of FD&C Yellow No. 5 and FD&C Yellow No. 5
Aluminum Lake for coloring drugs and cosmetics intended for use in the
area of the eye.
FDA gave interested persons until December 29, 1994, to file
objections or requests for a hearing. The agency received no objections
or requests for a hearing on the final rule. Therefore, FDA finds that
the final rule published in the Federal Register of November 29, 1994,
should be confirmed as corrected on December 2, 1994.
List of Subjects
21 CFR Part 74
Color additives, Cosmetics, Drugs.
21 CFR Part 201
Drugs, Labeling, Reporting and recordkeeping requirements.
Therefore, under the Federal Food, Drug, and Cosmetic Act (secs.
201, 401, 402, 403, 409, 501, 502, 505, 601, 602, 701, 721 (21 U.S.C.
321, 341, 342, 343, 348, 351, 352, 355, 361, 362, 371, 379e)) and under
authority delegated to the Commissioner of Food and Drugs (21 CFR
5.10), notice is given that no objections or requests for a hearing
were filed in response to the November 29, 1994, final rule.
Accordingly, the amendments promulgated thereby became effective
December 30, 1994.
Dated: January 19, 1995.
William K. Hubbard,
Interim Deputy Commissioner for Policy.
[FR Doc. 95-2005 Filed 1-25-95; 8:45 am]
BILLING CODE 4160-01-F
