Submission of Unreasonable Adverse Effects Information Under FIFRA Section 6(a)(2)

ICR 201408-2070-001

OMB: 2070-0039

Federal Form Document

Forms and Documents
Document
Name
Status
Supporting Statement A
2014-08-21
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
Supplementary Document
2014-08-15
IC Document Collections
ICR Details
2070-0039 201408-2070-001
Historical Active 201009-2070-001
EPA/OCSPP 1204.12
Submission of Unreasonable Adverse Effects Information Under FIFRA Section 6(a)(2)
Extension without change of a currently approved collection   No
Regular
Approved without change 09/08/2015
Retrieve Notice of Action (NOA) 09/15/2014
  Inventory as of this Action Requested Previously Approved
09/30/2018 36 Months From Approved 09/30/2015
112,985 0 91,979
272,246 0 203,236
0 0 0

Section 6(a)(2) of the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) requires pesticide registrants to submit information to the Agency which may be relevant to the balancing of the risks and benefits of a pesticide product. Specifically, registrants are required to submit any factual information that it acquires regarding adverse effects associated with its pesticidal products, and it is up to the Agency to determine whether or not that factual information constitutes an unreasonable adverse effect. In order to limit the amount of less meaningful information that might be submitted to the Agency, EPA has defined the scope of factual information that the registrant must submit. EPA regulations at 40 CFR 159 provide a detailed description of the reporting obligations of registrants under FIFRA section 6(a)(2). Potential respondents affected by the collection activities under this ICR include anyone who holds or ever held a registration for a pesticide product issued under FIFRA section 3 or 24(c). The North American Industrial Classification System (NAICS) code is 325320 (Pesticide and Other Agricultural Chemical Manufacturing).

US Code: 7 USC 136d(a)(2) Name of Law: Section 6(a)(2) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
  
None

Not associated with rulemaking

  79 FR 6897 02/05/2014
79 FR 54977 09/15/2014
No

3
IC Title Form No. Form Name
FIFRA Section 6(a)(2) Submissions - Incidents
FIFRA Section 6(a)(2) Submisssions - Studies
FIFRA Section 6(a)(2) - Training

  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 112,985 91,979 0 0 21,006 0
Annual Time Burden (Hours) 272,246 203,236 0 0 69,010 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No
This increase is due to an adjustment based on activities under the ICR during the current approval period. Specifically, EPA is increasing the number of potential responses and the number of registrants of products, which results in a small increase in the number of employees being trained. There is also an increase in incident information collected on spot-on treatments and neonicotinoid pesticides due to bee kills and colony loses.

$1,540,778
No
No
No
No
No
Uncollected
Angela Hofmann 202 260-2922 hofmann.angela@epamail.epa.gov

  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:
 
 
 
 
 
 
 
    (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;
 
 
 
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.
09/15/2014


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