Registrants Inventory of Drugs Surrendered

OMB Control No: 1117-0007	ICR Reference No: 201102-1117-002
Status: Historical Active	Previous ICR Reference No: 200712-1117-003
Agency/Subagency: DOJ/DEA	Agency Tracking No:
Title: Registrants Inventory of Drugs Surrendered
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 with change	Conclusion Date: 08/25/2011
Retrieve Notice of Action (NOA)	Date Received in OIRA: 06/29/2011
Terms of Clearance: DEA will submit a major revision to this form in the immediate future as part of its rulemaking on the disposal of controlled substances. DEA will address DEA Form 41 changes in detail in the NPRM preamble, the Paperwork Reduction Act analysis, and the regulatory text. If DEA does not submit a major revision to this form during this new clearance period, the agency will: • Insert a blank line between the signature box and the registrant’s DEA number on pg. 1 of the form; • Insert a short statement—“If you destroyed any controlled substance, please provide the following:”—above the DATE line on pg. 2 of the form; • Reduce the number of copies associated with the form.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/2014	36 Months From Approved	08/31/2011
Responses	22,500	0	22,500
Time Burden (Hours)	11,250	0	11,250
Cost Burden (Dollars)	18,900	0	0

---

Abstract: Title 21, CFR, 1307.21 requires that any registrant desiring to voluntarily dispose of controlled substances shall list these controlled substances on DEA Form 41 and submit the form to the nearest DEA office. The DEA 41 is used to account for destroyed controlled substances, and its use is mandatory.

---

Authorizing Statute(s): US Code: 21 USC 827 Name of Law: Records and Reports of Registrants

Citations for New Statutory Requirements: None

---

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

---

Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 10392	02/24/2011
30-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 24054	04/29/2011
Did the Agency receive public comments on this ICR? No

---

Number of Information Collection (IC) in this ICR: 1

IC Title Form No. Form Name Registrants Inventory of Drugs Surrendered--DEA Form 41 41 Registrants Inventory of Drugs Surrendered

---

ICR Summary 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	22,500	22,500	0	0	0	0
Annual Time Burden (Hours)	11,250	11,250	0	0	0	0
Annual Cost Burden (Dollars)	18,900	0	0	0	18,900	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:

---

Annual Cost to Federal Government: $141,044

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]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

Agency Contact: Cathy Gallagher 202 307-7297 [email protected]

---

Common Form ICR:  No

---

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: 06/29/2011

---