Amendments to General Regulations of the Food and Drug Administration; Technical Amendments, 69543 [2013-27773]
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Federal Register / Vol. 78, No. 224 / Wednesday, November 20, 2013 / Rules and Regulations
Pub. L. 101–649, 104 Stat. 4978, 5027 (8
U.S.C. 1184 note); sec. 303(a)(8), Pub. L. 102–
232, 105 Stat. 1733, 1748 (8 U.S.C. 1101
note); sec. 323(c), Pub. L. 103–206, 107 Stat.
2428; sec. 412(e), Pub. L. 105–277, 112 Stat.
2681 (8 U.S.C. 1182 note); sec. 2(d), Pub. L.
106–95, 113 Stat. 1312, 1316 (8 U.S.C. 1182
note); 29 U.S.C. 49k; Pub. L. 109–423, 120
Stat. 2900; 8 CFR 214.2(h)(4)(i); and 8 CFR
214.2(h)(6)(iii).
Subparts A and C issued under 8 U.S.C.
1101(a)(15)(H)(ii)(b) and 1184; 29 U.S.C. 49 et
seq.; and 8 CFR 214.2(h)(4)(i).
Subpart C—[Removed and Reserved]
2. Remove and reserve subpart C,
consisting of §§ 655.200 through
655.215.
■
Signed in Washington, DC, this 17th day of
October 2013.
Eric M. Seleznow,
Acting Assistant Secretary, Employment and
Training Administration.
[FR Doc. 2013–27693 Filed 11–19–13; 8:45 am]
BILLING CODE 4510–FP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 1
[Docket No. FDA–2010–N–0560]
Amendments to General Regulations
of the Food and Drug Administration;
Technical Amendments
AGENCY:
Food and Drug Administration,
HHS.
Final rule; technical
amendments.
ACTION:
The Food and Drug
Administration (FDA or we) published
a final rule in the Federal Register on
November 30, 2010, amending certain
regulations to include tobacco products,
where appropriate, in light of FDA’s
authority to regulate these products
under the Family Smoking Prevention
and Tobacco Control Act (Tobacco
Control Act). The final rule
inadvertently deleted an authority
citation and language related to the
definition of ‘‘package.’’ We are
restoring the inadvertent deletions and
making a corresponding technical
change.
pmangrum on DSK3VPTVN1PROD with RULES
SUMMARY:
This rule is effective November
20, 2013.
FOR FURTHER INFORMATION CONTACT:
Felicia Billingslea, Center for Food
Safety and Applied Nutrition (HFS–
820), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park,
MD 20740–3835, 240–402–2371.
DATES:
VerDate Mar<15>2010
13:56 Nov 19, 2013
Jkt 232001
We are
making technical amendments to our
regulations under 21 CFR part 1.
In the Federal Register of November
30, 2010 (75 FR 73951), we amended
certain regulations in part 1 (21 CFR
part 1), ‘‘General Enforcement
Regulations,’’ in light of our authority
under the Tobacco Control Act. The
final rule, among other things:
• Revised the authority citation for
part 1 by removing a reference to section
302 of the Federal Food, Drug, and
Cosmetic Act (FD&C Act) (21 U.S.C.
332);
• Revised § 1.1(c), ‘‘General,’’ by
removing the terms ‘‘package in § 1.20
and of’’, and
• Revised § 1.20, ‘‘Presence of
mandatory label information,’’ by
removing the terms ‘‘package in § 1.20
and of’’.
The preamble to the final rule
explained that the revisions to part 1
reflected our authority over tobacco
products under the Tobacco Control Act
(75 FR 73951 at 73952). However, the
revisions inadvertently created one
inconsistency (in that other provisions
in part 1 did, in fact, rely on section 302
of the FD&C Act as part of their legal
authority) or created confusion over
whether the definition of ‘‘package’’ was
limited to the regulations in part 1 or
whether it also applied to other FDA
regulations.
Therefore, through this rule, we are
amending part 1 as follows:
• We are restoring section 302 of the
FD&C Act to the authority citation for
part 1. Because the authority citation is
expressed in terms of the U.S. Code, the
amendment is to insert ‘‘332’’ in the list
of U.S. Code sections.
• We are revising § 1.1(c) to restore
the terms ‘‘package in § 1.20 and of’’.
• We are revising § 1.20 to add a
cross-reference to § 1.1(c).
Publication of this document
constitutes final action of these changes
under the Administrative Procedure Act
(5 U.S.C. 553). These amendments are
merely correcting inadvertent deletions.
FDA, therefore, for good cause, finds
under 5 U.S.C. 553(b)(3)(B) and (d)(3)
that notice and public comment are
unnecessary.
SUPPLEMENTARY INFORMATION:
List of Subjects in 21 CFR Part 1
Cosmetics, Drugs, Exports, Food
labeling, Imports, Labeling, Reporting
and recordkeeping requirements.
Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs, 21 CFR part 1 is
amended as follows:
PO 00000
Frm 00009
Fmt 4700
Sfmt 4700
69543
PART 1—GENERAL ENFORCEMENT
REGULATIONS
1. The authority citation for 21 CFR
part 1 is revised to read as follows:
■
Authority: 15 U.S.C. 1333, 1453, 1454,
1455, 4402; 19 U.S.C. 1490, 1491; 21 U.S.C.
321, 331, 332, 333, 334, 335a, 343, 350c,
350d, 352, 355, 360b, 362, 371, 374, 381, 382,
387, 387a, 387c, 393; 42 U.S.C. 216, 241, 243,
262, 264.
§ 1.1
[Amended]
2. Amend § 1.1 by adding the phrase
‘‘of package in § 1.20 and’’ after the
word ‘‘definition’’ in the first sentence
of paragraph (c).
■ 3. In § 1.20, revise the introductory
text to read as follows:
■
§ 1.20 Presence of mandatory label
information.
In the regulations specified in § 1.1(c)
of this chapter, the term package means
any container or wrapping in which any
food, drug, device, or cosmetic is
enclosed for use in the delivery or
display of such commodities to retail
purchasers, but does not include:
*
*
*
*
*
Dated: November 14, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–27773 Filed 11–19–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF LABOR
Occupational Safety and Health
Administration
29 CFR Part 1910
[Docket No. OSHA–2013–0010]
RIN 1218–AC80
Record Requirements in the
Mechanical Power Presses Standard
Occupational Safety and Health
Administration (OSHA), Labor.
ACTION: Direct final rule; request for
comments.
AGENCY:
OSHA is making two main
revisions to its Mechanical Power
Presses Standard. First, OSHA is
revising a provision that requires
employers to develop and maintain
certification records of periodic
inspections performed on the presses by
adding a requirement that they develop
and maintain certification records of
any maintenance and repairs they
perform on the presses during the
periodic inspections. Second, OSHA is
removing the requirement from another
provision that employers develop and
SUMMARY:
E:\FR\FM\20NOR1.SGM
20NOR1
]]>Agencies
[Federal Register Volume 78, Number 224 (Wednesday, November 20, 2013)]
[Rules and Regulations]
[Page 69543]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-27773]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
21 CFR Part 1
[Docket No. FDA-2010-N-0560]
Amendments to General Regulations of the Food and Drug
Administration; Technical Amendments
AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule; technical amendments.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) published a final
rule in the Federal Register on November 30, 2010, amending certain
regulations to include tobacco products, where appropriate, in light of
FDA's authority to regulate these products under the Family Smoking
Prevention and Tobacco Control Act (Tobacco Control Act). The final
rule inadvertently deleted an authority citation and language related
to the definition of ``package.'' We are restoring the inadvertent
deletions and making a corresponding technical change.
DATES: This rule is effective November 20, 2013.
FOR FURTHER INFORMATION CONTACT: Felicia Billingslea, Center for Food
Safety and Applied Nutrition (HFS-820), Food and Drug Administration,
5100 Paint Branch Pkwy., College Park, MD 20740-3835, 240-402-2371.
SUPPLEMENTARY INFORMATION: We are making technical amendments to our
regulations under 21 CFR part 1.
In the Federal Register of November 30, 2010 (75 FR 73951), we
amended certain regulations in part 1 (21 CFR part 1), ``General
Enforcement Regulations,'' in light of our authority under the Tobacco
Control Act. The final rule, among other things:
Revised the authority citation for part 1 by removing a
reference to section 302 of the Federal Food, Drug, and Cosmetic Act
(FD&C Act) (21 U.S.C. 332);
Revised Sec. 1.1(c), ``General,'' by removing the terms
``package in Sec. 1.20 and of'', and
Revised Sec. 1.20, ``Presence of mandatory label
information,'' by removing the terms ``package in Sec. 1.20 and of''.
The preamble to the final rule explained that the revisions to part
1 reflected our authority over tobacco products under the Tobacco
Control Act (75 FR 73951 at 73952). However, the revisions
inadvertently created one inconsistency (in that other provisions in
part 1 did, in fact, rely on section 302 of the FD&C Act as part of
their legal authority) or created confusion over whether the definition
of ``package'' was limited to the regulations in part 1 or whether it
also applied to other FDA regulations.
Therefore, through this rule, we are amending part 1 as follows:
We are restoring section 302 of the FD&C Act to the
authority citation for part 1. Because the authority citation is
expressed in terms of the U.S. Code, the amendment is to insert ``332''
in the list of U.S. Code sections.
We are revising Sec. 1.1(c) to restore the terms
``package in Sec. 1.20 and of''.
We are revising Sec. 1.20 to add a cross-reference to
Sec. 1.1(c).
Publication of this document constitutes final action of these
changes under the Administrative Procedure Act (5 U.S.C. 553). These
amendments are merely correcting inadvertent deletions. FDA, therefore,
for good cause, finds under 5 U.S.C. 553(b)(3)(B) and (d)(3) that
notice and public comment are unnecessary.
List of Subjects in 21 CFR Part 1
Cosmetics, Drugs, Exports, Food labeling, Imports, Labeling,
Reporting and recordkeeping requirements.
Therefore, under the Federal Food, Drug, and Cosmetic Act and under
authority delegated to the Commissioner of Food and Drugs, 21 CFR part
1 is amended as follows:
PART 1--GENERAL ENFORCEMENT REGULATIONS
0
1. The authority citation for 21 CFR part 1 is revised to read as
follows:
Authority: 15 U.S.C. 1333, 1453, 1454, 1455, 4402; 19 U.S.C.
1490, 1491; 21 U.S.C. 321, 331, 332, 333, 334, 335a, 343, 350c,
350d, 352, 355, 360b, 362, 371, 374, 381, 382, 387, 387a, 387c, 393;
42 U.S.C. 216, 241, 243, 262, 264.
Sec. 1.1 [Amended]
0
2. Amend Sec. 1.1 by adding the phrase ``of package in Sec. 1.20
and'' after the word ``definition'' in the first sentence of paragraph
(c).
0
3. In Sec. 1.20, revise the introductory text to read as follows:
Sec. 1.20 Presence of mandatory label information.
In the regulations specified in Sec. 1.1(c) of this chapter, the
term package means any container or wrapping in which any food, drug,
device, or cosmetic is enclosed for use in the delivery or display of
such commodities to retail purchasers, but does not include:
* * * * *
Dated: November 14, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013-27773 Filed 11-19-13; 8:45 am]
BILLING CODE 4160-01-P
