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ONE TIME Reporting Burden
Substances Generally Recognized as Safe: Notification Procedure
OMB: 0910-0342
IC ID: 223140
OMB.report
HHS/FDA
OMB 0910-0342
ICR 201907-0910-015
IC 223140
( )
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0342 can be found here:
2022-06-09 - Extension without change of a currently approved collection
Documents and Forms
Document Name
Document Type
Form FDA 3667
ONE TIME Reporting Burden
Form
FDA 3667 Generally Recognized as Safe (GRAS) Notice
Form FDA 3667.pdf
Form
Information Collection (IC) Details
View Information Collection (IC)
IC Title:
ONE TIME Reporting Burden
Agency IC Tracking Number:
Is this a Common Form?
No
IC Status:
Removed
Obligation to Respond:
Voluntary
CFR Citation:
21 CFR 170.210-170.270
21 CFR 570.120-570.270
21 CFR 170.285
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Form
FDA 3667
Generally Recognized as Safe (GRAS) Notice
Form FDA 3667.pdf
Yes
Yes
Fillable Fileable
Federal Enterprise Architecture Business Reference Module
Line of Business:
Health
Subfunction:
Consumer Health and Safety
Privacy Act System of Records
Title:
FR Citation:
Number of Respondents:
525
Number of Respondents for Small Entity:
0
Affected Public:
Private Sector
Private Sector:
Businesses or other for-profits
Percentage of Respondents Reporting Electronically:
70 %
Approved
Program Change Due to New Statute
Program Change Due to Agency Discretion
Change Due to Adjustment in Agency Estimate
Change Due to Potential Violation of the PRA
Previously Approved
Annual Number of Responses for this IC
0
0
0
-525
0
525
Annual IC Time Burden (Hours)
0
0
0
-46,725
0
46,725
Annual IC Cost Burden (Dollars)
0
0
0
0
0
0
Documents for IC
Title
Document
Date Uploaded
No associated records found
Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.