Request for Nominations for Candidates To Serve on the National Public Health Surveillance and Biosurveillance Advisory Committee (NPHSBAC), 72868 [2012-29478]
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Federal Register / Vol. 77, No. 235 / Thursday, December 6, 2012 / Notices
Kimberly S. Lane,
Deputy Director, Office of Scientific Integrity,
Office of the Associate Director for Science,
Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2012–29474 Filed 12–5–12; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
The Centers for Disease Control (CDC)/
Health Resources and Services
Administration (HRSA) Advisory
Committee on HIV, Viral Hepatitis and
STD Prevention and Treatment Notice
of Charter Renewal
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the CDC/
HRSA Advisory Committee on HIV,
Viral Hepatitis and STD Prevention and
Treatment, Department of Health and
Human Services, has been renewed for
a 2-year period through November 25,
2014.
Contact Person for More Information:
Kevin Fenton, M.D., Ph.D., Designated
Federal Officer, CDC/HRSA Advisory
Committee on HIV, Viral Hepatitis and
STD Prevention and Treatment,
Department of Health and Human
Services, CDC, 1600 Clifton Road, NE.,
Mailstop E07, Atlanta, Georgia 30333,
telephone (404) 639–8000 or fax (404)
639–8600.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: November 29, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
Request for Nominations for
Candidates To Serve on the National
Public Health Surveillance and
Biosurveillance Advisory Committee
(NPHSBAC)
BILLING CODE 4163–18–P
[FR Doc. 2012–29471 Filed 12–5–12; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Correction: This notice was published
in the Federal Register on November 1,
2012 Volume 77, Number 215, page
66620. This notice is to announce the
extension of submission for potential
nominees.
Nominations should be sent, in
writing, and postmarked by December
21, 2012: Vernellia Johnson,
Management and Program Analyst,
Public Health Surveillance and
Informatics Program Office, Centers for
Disease Control and Prevention, Office
of Surveillance, Epidemiology and
Laboratory Services Century, 1600
Clifton Road NE., MS E–97, Atlanta, GA
30333 or via email to hft9@cdc.gov.
Telephone and facsimile submissions
cannot be accepted.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities for both CDC and
the Agency for Toxic Substances and
Disease Registry.
Dated: November 30, 2012.
Cathy Ramadei,
Acting Director, Management Analysis and
Services Office, Centers for Disease Control
and Prevention (CDC).
[FR Doc. 2012–29478 Filed 12–5–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–D–1086]
Compliance Guidance for Small
Business Entities on Labeling and
Effectiveness Testing; Sunscreen Drug
Products for Over-the-Counter Human
Use; Notice of Availability
AGENCY:
Food and Drug Administration,
HHS.
mstockstill on DSK4VPTVN1PROD with
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing the
availability of a compliance guidance
for small business entities entitled
‘‘Labeling and Effectiveness Testing:
SUMMARY:
VerDate Mar<15>2010
16:42 Dec 05, 2012
Jkt 229001
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
Sunscreen Drug Products for Over-theCounter Human Use; Small Entity
Compliance Guide.’’ This guidance is
intended to help small businesses
understand and comply with the
requirements of the final rule addressing
labeling and effectiveness testing
requirements for over-the counter (OTC)
sunscreen drug products. The guidance
describes the requirements of the final
rule in plain language and provides
answers to common questions on how
to comply with the rule. This guidance
was prepared in accordance with the
Small Business Regulatory Enforcement
Fairness Act.
DATES: Submit either electronic or
written comments on Agency guidances
at any time.
ADDRESSES: Submit written requests for
single copies of this guidance to the
Division of Drug Information, Center for
Drug Evaluation and Research, Food
and Drug Administration, 10903 New
Hampshire Ave., Bldg. 51, Rm. 2201,
Silver Spring, MD 20993–0002. Send
one self-addressed adhesive label to
assist that office in processing your
requests. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the guidance document.
Submit electronic comments on the
guidance to https://www.regulations.gov.
Submit written comments to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Reynold Tan, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, Rm. 5493,
Silver Spring, MD 20993–0002, 301–
796–1009.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is announcing the availability of
a compliance guidance for small
business entities entitled ‘‘Labeling and
Effectiveness Testing: Sunscreen Drug
Products for Over-the-Counter Human
Use; Small Entity Compliance Guide.’’
This guidance summarizes the June 17,
2011, final rule (76 FR 35620) regarding
labeling and testing requirements for
OTC sunscreen drug products. Under
the 2011 sunscreen final rule, required
and permitted labeling is based upon
the results of effectiveness testing. The
effectiveness testing consists of a sun
protection factor (SPF) Test and a Broad
Spectrum (ultraviolet A (UVA) and
ultraviolet B (UVB) protection) Test. In
addition, a test demonstrating water
resistance that accompanies the SPF
Test to ensure retention of SPF
E:\FR\FM\06DEN1.SGM
06DEN1
Agencies
[Federal Register Volume 77, Number 235 (Thursday, December 6, 2012)]
[Notices]
[Page 72868]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-29478]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Request for Nominations for Candidates To Serve on the National
Public Health Surveillance and Biosurveillance Advisory Committee
(NPHSBAC)
Correction: This notice was published in the Federal Register on
November 1, 2012 Volume 77, Number 215, page 66620. This notice is to
announce the extension of submission for potential nominees.
Nominations should be sent, in writing, and postmarked by December
21, 2012: Vernellia Johnson, Management and Program Analyst, Public
Health Surveillance and Informatics Program Office, Centers for Disease
Control and Prevention, Office of Surveillance, Epidemiology and
Laboratory Services Century, 1600 Clifton Road NE., MS E-97, Atlanta,
GA 30333 or via email to hft9@cdc.gov. Telephone and facsimile
submissions cannot be accepted.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining to
announcements of meetings and other committee management activities for
both CDC and the Agency for Toxic Substances and Disease Registry.
Dated: November 30, 2012.
Cathy Ramadei,
Acting Director, Management Analysis and Services Office, Centers for
Disease Control and Prevention (CDC).
[FR Doc. 2012-29478 Filed 12-5-12; 8:45 am]
BILLING CODE 4163-18-P