Color Additive Requests and Recordkeeping

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
0216 21 CFR 80 39.doc	Supplementary Document	Uploaded 2007-11-16	Available
0216 21 CFR 80 22.doc	Supplementary Document	Uploaded 2007-11-16	Available
0216 21 CFR 80 21.doc	Supplementary Document	Uploaded 2007-11-16	Available
0216 Section 721a of the FFDCA.doc	Supplementary Document	Uploaded 2007-11-16	Available
0216 ss 11-15-2007.doc	Supporting Statement A	Uploaded 2007-11-16	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
5817	Color Additive Requests and Recordkeeping		Modified
182949	Color Additive Requests and Recordkeeping		New
182948	Color Additive Requests and Recordkeeping		New

ICR Details

OMB Control No: 0910-0216	ICR Reference No: 200712-0910-001
Status: Historical Active	Previous ICR Reference No: 200408-0910-005
Agency/Subagency: HHS/FDA	Agency Tracking No:
Title: Color Additive Requests and Recordkeeping
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 02/11/2008
Retrieve Notice of Action (NOA)	Date Received in OIRA: 12/10/2007
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2011	36 Months From Approved	02/29/2008
Responses	16,704	0	4,603
Time Burden (Hours)	2,784	0	2,302
Cost Burden (Dollars)	0	0	0

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Abstract: Section 721 of the Federal Food, Drug, and Cosmetic Act requires FDA to batch certify the color additives listed in 21 CFR parts 74 and 82. FDA's Color Certification Program described in 21 CFR part 80, requires submission to FDA of manufacturer information for each new batch of color additive, FDA analysis of a representative sample of the batch, and issuance of a certification lot number for the batch upon completion of the certification process.

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Authorizing Statute(s): US Code: 21 USC 379 Name of Law: FFDCA
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	72 FR 40310	07/24/2007
30-day Notice:	Federal Register Citation:	Citation Date:
	72 FR 67942	12/03/2007
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 3

table that charts list of burden

IC Title	Form No.	Form Name
Color Additive Requests and Recordkeeping
Color Additive Requests and Recordkeeping
Color Additive Requests and Recordkeeping

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ICR Summary of Burden

table that charts list of burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	16,704	4,603	0	0	12,101	0
Annual Time Burden (Hours)	2,784	2,302	0	0	482	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 12/10/2007

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