[Federal Register Volume 75, Number 240 (Wednesday, December 15, 2010)]
[Notices]
[Pages 78257-78259]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-31386]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2010-N-0623]
Agency Information Collection Activities; Proposed Collection;
Comment Request; Voluntary Cosmetic Registration Program
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing an
opportunity for public comment on the proposed collection of certain
information by the Agency. Under the Paperwork Reduction Act of 1995
(the PRA), Federal Agencies are required to publish notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice. This notice solicits comments on the collection of information
associated with the Agency's Voluntary Cosmetic Registration Program
(VCRP).
DATES: Submit either electronic or written comments on the collection
of information by February 14, 2011.
ADDRESSES: Submit electronic comments on the collection of information
to http://www.regulations.gov. Submit written comments on the
collection of information to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852. All comments should be identified with the docket
number found in brackets in the heading of this document.
FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of
Information Management, Food and Drug Administration, 1350 Piccard Dr.,
PI50-400B, Rockville, MD 20850. 301-796-3793.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
Agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes Agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A))
requires Federal Agencies to provide a 60-day notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information,
before submitting the collection to OMB for approval. To comply with
this requirement, FDA is publishing notice of the proposed collection
of information set forth in this document.
With respect to the following collection of information, FDA
invites comments on these topics: (1) Whether the proposed collection
of information is necessary for the proper performance of FDA's
functions, including whether the information will have practical
utility; (2) the accuracy of FDA's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques, when
appropriate, and other forms of information technology.
Voluntary Cosmetic Registration Program--21 CFR Parts 710 and 720 (OMB
Control Number 0910-0027)--Revision
The Federal Food, Drug, and Cosmetic Act (the FD&C Act) provides
FDA with the authority to regulate cosmetic products in the United
States. Cosmetic products that are adulterated under section 601 of the
FD&C Act (21 U.S.C. 361) or misbranded under section 602 of the FD&C
Act (21 U.S.C. 362) may not be distributed in interstate commerce. To
assist FDA in carrying out its responsibility to regulate cosmetics,
the Agency has developed the VCRP.
In 21 CFR part 710, FDA requests that establishments that
manufacture or package cosmetic products register with the Agency on
Form FDA 2511 entitled ``Registration of Cosmetic Product
Establishment.'' The term ``Form FDA 2511'' refers to both the paper
and electronic versions of the form. The electronic version of Form FDA
2511 is available on FDA's VCRP Web site at http://www.fda.gov/Cosmetics/GuidanceComplianceRegulatoryInformation/VoluntaryCosmeticsRegistrationProgramVCRP/OnlineRegistration/default.htm. FDA's online registration system, intended to make it
easier to participate in the VCRP, was made available industrywide on
December 1, 2005. The Agency strongly encourages electronic
registration of Form FDA 2511 because it is faster and more convenient.
A registering facility will receive confirmation of electronic
registration, including a registration number, by e-mail, usually
within 7 business days. The online system also allows for amendments to
past submissions.
Because registration of cosmetic product establishments is not
mandatory, voluntary registration provides FDA with the best
information available about the locations, business trade names, and
types of activity (manufacturing or packaging) of cosmetic product
establishments. FDA places the registration information in a computer
database and uses the information to generate mailing lists for
distributing regulatory information and for inviting firms to
participate in workshops on topics in which they may be interested. FDA
also uses the
[[Page 78258]]
information for estimating the size of the cosmetic industry and for
conducting onsite establishment inspections. Registration is permanent,
although FDA requests that respondents submit an amended Form FDA 2511
if any of the originally submitted information changes.
In part 720 (21 CFR part 720), FDA requests that firms that
manufacture, pack, or distribute cosmetics file with the Agency an
ingredient statement for each of their products. Ingredient statements
for new submissions (Sec. Sec. 720.1 through 720.4) are reported on
Form FDA 2512, ``Cosmetic Product Ingredient Statement,'' and on Form
FDA 2512a, a continuation form. Amendments to product formulations
(Sec. 720.6) also are reported on Forms FDA 2512 and FDA 2512a. When a
firm discontinues the commercial distribution of a cosmetic, FDA
requests that the firm file Form FDA 2514, ``Notice of Discontinuance
of Commercial Distribution of Cosmetic Product Formulation''
(Sec. Sec. 720.3 and 720.6). If any of the information submitted on or
with these forms is confidential, the firm may submit a request for
confidentiality under Sec. 720.8.
FDA's online filing system is available on FDA's VCRP Web site at
http://wcms.fda.gov/FDAgov/Cosmetics/GuidanceComplianceRegulatoryInformation/VoluntaryCosmeticsRegistrationProgramVCRP/OnlineRegistration/default.htm. The online filing system contains the electronic versions
of Forms FDA 2512, 2512a, and 2514, which are collectively found within
the electronic version of Form FDA 2512. The Agency strongly encourages
electronic filing of Form FDA 2512 because it is faster and more
convenient. A filer will receive confirmation of electronic filing by
e-mail.
FDA places cosmetic product filing information in a computer
database and uses the information for evaluation of cosmetic products
currently on the market. Because filing of cosmetic product
formulations is not mandatory, voluntary filings provide FDA with the
best information available about cosmetic product ingredients and their
frequency of use, businesses engaged in the manufacture and
distribution of cosmetics, and approximate rates of product
discontinuance and formula modifications. The information assists FDA
scientists in evaluating reports of alleged injuries and adverse
reactions from the use of cosmetics. The information also is used in
defining and planning analytical and toxicological studies pertaining
to cosmetics.
Information from the database is releasable to the public under FDA
compliance with the Freedom of Information Act. FDA shares
nonconfidential information from its files on cosmetics with consumers,
medical professionals, and industry.
FDA estimates the burden of this collection of information as
follows:
Table 1--Estimated Annual Reporting Burden \1\
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Annual
21 CFR section or part Form No. Number of frequency per Total annual Hours per Total hours
respondents response responses response
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Part 710 (registrations)................... FDA 2511 \2\................. 135 1 135 0.2 27
720.1 through 720.4 (new submissions)...... FDA 2512 \3\................. 141 31 4,371 0.33 1,442
720.6 (amendments)......................... FDA 2512..................... 109 7 763 0.17 130
720.6 (notices of discontinuance).......... FDA 2512..................... 55 41 2,255 0.1 226
720.8 (requests for confidentiality)....... ............................. 1 1 1 2.0 2.0
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Total.................................. ............................. .............. .............. .............. ............. 1,827
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\1\ There are no capital costs or operating and maintenance costs associated with this collection of information.
\2\ The term ``Form FDA 2511'' refers to both the paper Forms FDA 2511 and electronic Form FDA 2511 in the electronic system known as the Voluntary
Cosmetic Registration Program, which is available at http://wcms.fda.gov/FDAgov/Cosmetics/GuidanceComplianceRegulatoryInformation/VoluntaryCosmeticsRegistrationProgramVCRP/OnlineRegistration/default.htm.
\3\ The term ``Form FDA 2512'' refers to the paper Forms FDA 2512, 2512a, and 2514 and electronic Form FDA 2512 in the electronic system known as the
Voluntary Cosmetic Registration Program, which is available at http://wcms.fda.gov/FDAgov/Cosmetics/GuidanceComplianceRegulatoryInformation/VoluntaryCosmeticsRegistrationProgramVCRP/OnlineRegistration/default.htm.
FDA bases its estimate of the number of responses on submissions
received from fiscal years 2005 to 2007. FDA bases its estimate of the
hours per response upon information from cosmetic industry personnel
and FDA experience entering data submitted on paper Forms 2511, 2512,
2512a, and 2514. FDA estimates that, annually, 135 establishments that
manufacture or package cosmetic products will each submit 1
registration on Form FDA 2511, for a total of 135 annual responses.
Each submission is estimated to take 0.2 hour per response for a total
of 27 hours. FDA estimates that, annually, 141 firms that manufacture,
pack, or distribute cosmetics will file 31 ingredient statements for
new submissions on Forms FDA 2512 and FDA 2512a, for a total of 4,371
annual responses. Each submission is estimated to take 0.33 hour per
response for a total of 1,442.43 hours, rounded to 1,442. FDA estimates
that, annually, 109 firms that manufacture, pack, or distribute
cosmetics will file 7 amendments to product formulations on Forms FDA
2512 and FDA 2512a, for a total of 763 annual responses. Each
submission is estimated to take 0.17 hour per response for a total of
129.71 hours, rounded to 130. FDA estimates that, annually, 55 firms
that manufacture, pack, or distribute cosmetics will file 41 notices of
discontinuance on Form FDA 2514, for a total of 2,255 annual responses.
Each submission is estimated to take 0.1 hour per response for a total
of 225.50 hours, rounded to 226. FDA estimates that, annually, one firm
will file one request for confidentiality. Each such request is
estimated to take 2 hours to prepare for a total of 2.0 hours. Thus,
the total estimated hour burden for this information collection is
1,827 hours.
This is a revision request in which the burden hours for the
information collection request (ICR) under OMB control number 0910-
0030, ``Cosmetic Product Voluntary Reporting Program'' are being
consolidated under the ICR assigned OMB control number 0910-0027,
``Voluntary Registration of Cosmetic Product Establishments,'' which
expires February 28, 2011. The revised ICR for 0910-0027 has been
renamed ``Voluntary Cosmetic Registration Program.'' Upon approval of
this revision request, the ICR for 0910-0030 will be discontinued.
[[Page 78259]]
Dated: December 9, 2010.
Leslie Kux,
Acting Assistant, Commissioner for Policy.
[FR Doc. 2010-31386 Filed 12-14-10; 8:45 am]
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