Inorganic Arsenic in Rice Cereals for Infants: Action Level; Guidance for Industry; Availability, 47797-47798 [2020-17169]
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Federal Register / Vol. 85, No. 152 / Thursday, August 6, 2020 / Notices
companies registered multiple facilities
in a single email.
Based on our experience with a
similar information collection, upon
requesting to be placed on the list, data
elements that may be provided to China
include the facility name, street address,
city, State, and ZIP code of U.S.
manufacturers and processors of
covered products, who want to be
included on the list sent to China.
Manufacturers of these products must
currently register with FDA consistent
with 21 CFR part 1, subpart H.
Therefore, we believe burden associated
with this collection should be minimal,
but we welcome specific feedback in
this regard.
Dated: July 30, 2020.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2020–17161 Filed 8–5–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–D–1099]
Inorganic Arsenic in Rice Cereals for
Infants: Action Level; Guidance for
Industry; Availability
Food and Drug Administration,
Health and Human Services (HHS).
ACTION: Notice of availability.
AGENCY:
The Food and Drug
Administration (FDA or we) is
announcing the availability of a final
guidance for industry entitled
‘‘Inorganic Arsenic in Rice Cereals for
Infants: Action Level.’’ The guidance
identifies for industry an action level for
inorganic arsenic in rice cereals for
infants that is intended to help protect
public health and is achievable with the
use of current good manufacturing
practices. It also describes our intended
sampling and enforcement approach.
Thus, the guidance finalizes the
approach presented in the draft
guidance issued in 2016.
DATES: The announcement of the
guidance is published in the Federal
Register on August 6, 2020.
ADDRESSES: You may submit either
electronic or written comments on FDA
guidances at any time as follows:
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
VerDate Sep<11>2014
17:13 Aug 05, 2020
Jkt 250001
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2016–D–1099 for ‘‘Inorganic Arsenic in
Rice Cereals for Infants: Action Level;
Guidance for Industry.’’ Received
comments will be placed in the docket
and, except for those submitted as
‘‘Confidential Submissions,’’ publicly
viewable at https://www.regulations.gov
or at the Dockets Management Staff
between 9 a.m. and 4 p.m., Monday
through Friday, 240–402–7500.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION.’’ We
will review this copy, including the
claimed confidential information, in our
consideration of comments. The second
copy, which will have the claimed
confidential information redacted/
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
47797
blacked out, will be available for public
viewing and posted on https://
www.regulations.gov. Submit both
copies to the Dockets Management Staff.
If you do not wish your name and
contact information to be made publicly
available, you can provide this
information on the cover sheet and not
in the body of your comments and you
must identify this information as
‘‘confidential.’’ Any information marked
as ‘‘confidential’’ will not be disclosed
except in accordance with 21 CFR 10.20
and other applicable disclosure law. For
more information about FDA’s posting
of comments to public dockets, see 80
FR 56469, September 18, 2015, or access
the information at: https://
www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852, 240–402–7500.
You may submit comments on any
guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single
copies of the guidance to Division of
Plant Products and Beverages, Office of
Food Safety, Center for Food Safety and
Applied Nutrition, Food and Drug
Administration (HFS–317), 5001
Campus Dr., College Park, MD 20740.
Send two self-addressed adhesive labels
to assist that office in processing your
request. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the guidance.
FOR FURTHER INFORMATION CONTACT:
Eileen Abt, Center for Food Safety and
Applied Nutrition (HFS–317), Food and
Drug Administration, 5001 Campus Dr.,
College Park, MD 20740, 240–402–1529.
SUPPLEMENTARY INFORMATION:
I. Background
We are announcing the availability of
a guidance for industry entitled
‘‘Inorganic Arsenic in Rice Cereals for
Infants: Action Level.’’ We are issuing
this guidance consistent with our good
guidance practices regulation (21 CFR
10.115). The guidance represents the
current thinking of FDA on this topic.
It does not establish any rights for any
person and is not binding on FDA or the
public. You can use an alternative
approach if it satisfies the requirements
of the applicable statutes and
regulations.
E:\FR\FM\06AUN1.SGM
06AUN1
jbell on DSKJLSW7X2PROD with NOTICES
47798
Federal Register / Vol. 85, No. 152 / Thursday, August 6, 2020 / Notices
In the Federal Register of April 6,
2016 (81 FR 19976), we made available
a draft guidance for industry entitled
‘‘Inorganic Arsenic in Rice Cereals for
Infants: Action Level.’’ We also
announced the availability of two
related scientific documents: a
document entitled ‘‘Supporting
Document for Action Level for Inorganic
Arsenic in Rice Cereals for Infants’’
(supporting document), and a risk
assessment entitled ‘‘Arsenic in Rice
and Rice Products Risk Assessment:
Report’’ (the risk assessment report). We
gave interested parties an opportunity to
submit comments by July 5, 2016, and
later extended the comment period to
July 19, 2016 (see 81 FR 42714 (June 30,
2016)).
This guidance finalizes FDA’s action
level for inorganic arsenic in rice cereals
for infants of 100 micrograms per
kilogram (mg/kg) or 100 parts per billion
(ppb) and identifies FDA’s intended
sampling and enforcement approach.
The basis for the action level is set forth
in the revised supporting document.
The revised supporting document as
well as the risk assessment report
originally made available on April 6,
2016 (81 FR 19976), can be accessed at
www.regulations.gov. The revised
supporting document reviews data on
inorganic arsenic levels in rice cereals
for infants, health effects, and
achievability and explains FDA’s
rationale for identifying an action level
of 100 mg/kg for inorganic arsenic in rice
cereals for infants.
Arsenic is present in the environment
as a naturally occurring substance or as
a result of contamination from human
activity. In foods, arsenic may be
present as inorganic arsenic (the
primary toxic form of arsenic) or organic
arsenic. Exposure to inorganic arsenic is
associated with adverse human health
effects including cancer and
neurodevelopmental effects. Rice and
rice products are common in the
American diet, and FDA sampling data
have demonstrated that rice and rice
products have higher levels of inorganic
arsenic than other foods. Furthermore,
rice and rice products are a greater
potential source of dietary inorganic
arsenic exposure for infants and
children than for adults, because the
dietary patterns of infants and children
are often less varied than those of
adults, and because infants and children
consume more food relative to their
body weight than do adults. We expect
that that the 100 mg/kg action level,
though non-binding, will help protect
the public health, by encouraging
manufacturers to reduce levels of
inorganic arsenic in rice cereals for
infants, and we also expect that this
VerDate Sep<11>2014
17:13 Aug 05, 2020
Jkt 250001
level is achievable by industry with the
use of current good manufacturing
practices. We intend to consider the
action level of 100 mg/kg or 100 ppb
inorganic arsenic as an important source
of information for determining whether
infant rice cereal is adulterated within
the meaning of section 402(a)(1) of the
Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 342(a)(1)).
Comments on the draft guidance
requested that we consider establishing
action levels for rice-based foods other
than infant cereal, lower the action level
under 100 ppb, and questioned the
achievability of the action level of 100
ppb for inorganic arsenic in infant rice
cereals. However, we did not receive
new data from the comments supporting
establishment of either lower or higher
action levels. We determined that we
should prioritize efforts to reduce infant
exposure to inorganic arsenic from rice
because rice intake, primarily through
infant rice cereal, is about three times
greater for infants than adults in relation
to body weight (Ref. 1), and
epidemiologic data show that early life
exposure to inorganic arsenic, including
dietary exposure, can result in a child’s
decreased performance on certain
developmental tests that measure
learning (Ref. 1). Thus, the guidance
finalizes the approach presented in the
draft guidance.
Other comments suggested
modifications to the risk assessment
report. We note that the risk assessment
report underwent extensive interagency
review and external peer review before
we made it available to the public. None
of these comments supported a
determination that the risk assessment
report needs to be modified. We will
continue to monitor research
developments on non-cancer adverse
health effects, such as
neurodevelopmental effects,
cardiovascular disease, and diabetes, to
determine if new data support changes
to the risk assessment report or
guidance.
II. Paperwork Reduction Act of 1995
This guidance contains no collection
of information. Therefore, clearance by
the Office of Management and Budget
under the Paperwork Reduction Act is
not required.
III. Electronic Access
Persons with access to the internet
may obtain the guidance at either
https://www.fda.gov/FoodGuidances or
https://www.regulations.gov. Use the
FDA website listed in the previous
sentence to find the most current
version of the guidance.
PO 00000
Frm 00070
Fmt 4703
Sfmt 4703
IV. References
The following references are on
display at the Dockets Management Staff
(see ADDRESSES) and are available for
viewing by interested persons between
9 a.m. and 4 p.m., Monday through
Friday; they are also available
electronically at https://
www.regulations.gov. FDA has verified
the website addresses, as of the date this
document publishes in the Federal
Register, but websites are subject to
change over time.
1. FDA, ‘‘Arsenic in Rice and Rice Products
Risk Assessment: Report,’’ 2016, https://
www.fda.gov/Food/FoodScienceResearch/
RiskSafetyAssessment/ucm485278.htm.
Dated: July 29, 2020.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2020–17169 Filed 8–5–20; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2020–N–0955]
Phibro Animal Health Corp.; Carbadox
in Medicated Swine Feed; Revocation
of Approved Method; Correction
Food and Drug Administration,
Health and Human Services (HHS).
AGENCY:
ACTION:
Proposed order; correction.
The Food and Drug
Administration (FDA) is correcting a
proposed order to revoke the approved
method for detecting residues of
carbadox, a carcinogenic new animal
drug used in swine feed. The document
was published with an incorrect docket
number. This document corrects that
error.
SUMMARY:
FOR FURTHER INFORMATION CONTACT:
Diane Heinz, Center for Veterinary
Medicine (HFV–6), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240–402–5692,
diane.heinz@fda.hhs.gov.
In the
Federal Register of July 20, 2020, in FR
Doc. 2020–15246, on page 43853, the
following correction is made:
On page 43853, in the second column,
in the header of the document, and also
in the third column under Instructions,
‘‘Docket No. FDA–2016–N–0832’’ is
corrected to read ‘‘Docket No. FDA–
2020–N–0955’’.
SUPPLEMENTARY INFORMATION:
E:\FR\FM\06AUN1.SGM
06AUN1
Agencies
[Federal Register Volume 85, Number 152 (Thursday, August 6, 2020)]
[Notices]
[Pages 47797-47798]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-17169]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2016-D-1099]
Inorganic Arsenic in Rice Cereals for Infants: Action Level;
Guidance for Industry; Availability
AGENCY: Food and Drug Administration, Health and Human Services (HHS).
ACTION: Notice of availability.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA or we) is announcing the
availability of a final guidance for industry entitled ``Inorganic
Arsenic in Rice Cereals for Infants: Action Level.'' The guidance
identifies for industry an action level for inorganic arsenic in rice
cereals for infants that is intended to help protect public health and
is achievable with the use of current good manufacturing practices. It
also describes our intended sampling and enforcement approach. Thus,
the guidance finalizes the approach presented in the draft guidance
issued in 2016.
DATES: The announcement of the guidance is published in the Federal
Register on August 6, 2020.
ADDRESSES: You may submit either electronic or written comments on FDA
guidances at any time as follows:
Electronic Submissions
Submit electronic comments in the following way:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments. Comments submitted
electronically, including attachments, to https://www.regulations.gov
will be posted to the docket unchanged. Because your comment will be
made public, you are solely responsible for ensuring that your comment
does not include any confidential information that you or a third party
may not wish to be posted, such as medical information, your or anyone
else's Social Security number, or confidential business information,
such as a manufacturing process. Please note that if you include your
name, contact information, or other information that identifies you in
the body of your comments, that information will be posted on https://www.regulations.gov.
If you want to submit a comment with confidential
information that you do not wish to be made available to the public,
submit the comment as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For written/paper comments submitted to the Dockets
Management Staff, FDA will post your comment, as well as any
attachments, except for information submitted, marked and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All submissions received must include the Docket No.
FDA-2016-D-1099 for ``Inorganic Arsenic in Rice Cereals for Infants:
Action Level; Guidance for Industry.'' Received comments will be placed
in the docket and, except for those submitted as ``Confidential
Submissions,'' publicly viewable at https://www.regulations.gov or at
the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through
Friday, 240-402-7500.
Confidential Submissions--To submit a comment with
confidential information that you do not wish to be made publicly
available, submit your comments only as a written/paper submission. You
should submit two copies total. One copy will include the information
you claim to be confidential with a heading or cover note that states
``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' We will review
this copy, including the claimed confidential information, in our
consideration of comments. The second copy, which will have the claimed
confidential information redacted/blacked out, will be available for
public viewing and posted on https://www.regulations.gov. Submit both
copies to the Dockets Management Staff. If you do not wish your name
and contact information to be made publicly available, you can provide
this information on the cover sheet and not in the body of your
comments and you must identify this information as ``confidential.''
Any information marked as ``confidential'' will not be disclosed except
in accordance with 21 CFR 10.20 and other applicable disclosure law.
For more information about FDA's posting of comments to public dockets,
see 80 FR 56469, September 18, 2015, or access the information at:
https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket to read background documents or
the electronic and written/paper comments received, go to https://www.regulations.gov and insert the docket number, found in brackets in
the heading of this document, into the ``Search'' box and follow the
prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane,
Rm. 1061, Rockville, MD 20852, 240-402-7500.
You may submit comments on any guidance at any time (see 21 CFR
10.115(g)(5)).
Submit written requests for single copies of the guidance to
Division of Plant Products and Beverages, Office of Food Safety, Center
for Food Safety and Applied Nutrition, Food and Drug Administration
(HFS-317), 5001 Campus Dr., College Park, MD 20740. Send two self-
addressed adhesive labels to assist that office in processing your
request. See the SUPPLEMENTARY INFORMATION section for electronic
access to the guidance.
FOR FURTHER INFORMATION CONTACT: Eileen Abt, Center for Food Safety and
Applied Nutrition (HFS-317), Food and Drug Administration, 5001 Campus
Dr., College Park, MD 20740, 240-402-1529.
SUPPLEMENTARY INFORMATION:
I. Background
We are announcing the availability of a guidance for industry
entitled ``Inorganic Arsenic in Rice Cereals for Infants: Action
Level.'' We are issuing this guidance consistent with our good guidance
practices regulation (21 CFR 10.115). The guidance represents the
current thinking of FDA on this topic. It does not establish any rights
for any person and is not binding on FDA or the public. You can use an
alternative approach if it satisfies the requirements of the applicable
statutes and regulations.
[[Page 47798]]
In the Federal Register of April 6, 2016 (81 FR 19976), we made
available a draft guidance for industry entitled ``Inorganic Arsenic in
Rice Cereals for Infants: Action Level.'' We also announced the
availability of two related scientific documents: a document entitled
``Supporting Document for Action Level for Inorganic Arsenic in Rice
Cereals for Infants'' (supporting document), and a risk assessment
entitled ``Arsenic in Rice and Rice Products Risk Assessment: Report''
(the risk assessment report). We gave interested parties an opportunity
to submit comments by July 5, 2016, and later extended the comment
period to July 19, 2016 (see 81 FR 42714 (June 30, 2016)).
This guidance finalizes FDA's action level for inorganic arsenic in
rice cereals for infants of 100 micrograms per kilogram ([micro]g/kg)
or 100 parts per billion (ppb) and identifies FDA's intended sampling
and enforcement approach. The basis for the action level is set forth
in the revised supporting document. The revised supporting document as
well as the risk assessment report originally made available on April
6, 2016 (81 FR 19976), can be accessed at www.regulations.gov. The
revised supporting document reviews data on inorganic arsenic levels in
rice cereals for infants, health effects, and achievability and
explains FDA's rationale for identifying an action level of 100
[micro]g/kg for inorganic arsenic in rice cereals for infants.
Arsenic is present in the environment as a naturally occurring
substance or as a result of contamination from human activity. In
foods, arsenic may be present as inorganic arsenic (the primary toxic
form of arsenic) or organic arsenic. Exposure to inorganic arsenic is
associated with adverse human health effects including cancer and
neurodevelopmental effects. Rice and rice products are common in the
American diet, and FDA sampling data have demonstrated that rice and
rice products have higher levels of inorganic arsenic than other foods.
Furthermore, rice and rice products are a greater potential source of
dietary inorganic arsenic exposure for infants and children than for
adults, because the dietary patterns of infants and children are often
less varied than those of adults, and because infants and children
consume more food relative to their body weight than do adults. We
expect that that the 100 [micro]g/kg action level, though non-binding,
will help protect the public health, by encouraging manufacturers to
reduce levels of inorganic arsenic in rice cereals for infants, and we
also expect that this level is achievable by industry with the use of
current good manufacturing practices. We intend to consider the action
level of 100 [micro]g/kg or 100 ppb inorganic arsenic as an important
source of information for determining whether infant rice cereal is
adulterated within the meaning of section 402(a)(1) of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C. 342(a)(1)).
Comments on the draft guidance requested that we consider
establishing action levels for rice-based foods other than infant
cereal, lower the action level under 100 ppb, and questioned the
achievability of the action level of 100 ppb for inorganic arsenic in
infant rice cereals. However, we did not receive new data from the
comments supporting establishment of either lower or higher action
levels. We determined that we should prioritize efforts to reduce
infant exposure to inorganic arsenic from rice because rice intake,
primarily through infant rice cereal, is about three times greater for
infants than adults in relation to body weight (Ref. 1), and
epidemiologic data show that early life exposure to inorganic arsenic,
including dietary exposure, can result in a child's decreased
performance on certain developmental tests that measure learning (Ref.
1). Thus, the guidance finalizes the approach presented in the draft
guidance.
Other comments suggested modifications to the risk assessment
report. We note that the risk assessment report underwent extensive
interagency review and external peer review before we made it available
to the public. None of these comments supported a determination that
the risk assessment report needs to be modified. We will continue to
monitor research developments on non-cancer adverse health effects,
such as neurodevelopmental effects, cardiovascular disease, and
diabetes, to determine if new data support changes to the risk
assessment report or guidance.
II. Paperwork Reduction Act of 1995
This guidance contains no collection of information. Therefore,
clearance by the Office of Management and Budget under the Paperwork
Reduction Act is not required.
III. Electronic Access
Persons with access to the internet may obtain the guidance at
either https://www.fda.gov/FoodGuidances or https://www.regulations.gov. Use the FDA website listed in the previous
sentence to find the most current version of the guidance.
IV. References
The following references are on display at the Dockets Management
Staff (see ADDRESSES) and are available for viewing by interested
persons between 9 a.m. and 4 p.m., Monday through Friday; they are also
available electronically at https://www.regulations.gov. FDA has
verified the website addresses, as of the date this document publishes
in the Federal Register, but websites are subject to change over time.
1. FDA, ``Arsenic in Rice and Rice Products Risk Assessment:
Report,'' 2016, https://www.fda.gov/Food/FoodScienceResearch/RiskSafetyAssessment/ucm485278.htm.
Dated: July 29, 2020.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2020-17169 Filed 8-5-20; 8:45 am]
BILLING CODE 4164-01-P