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This document details the approval of an amended labeling for Turf Fertilizer with Prodiamine 0.75%, which includes changes to state restrictions, use restrictions, agricultural use requirements, label claims, and typographical corrections. It outlines the acceptable use and distribution of the product along with necessary precautions and application guidelines as per EPA regulations.
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How to fill out non-pria labeling amendment

01
Identify the product for which you need to submit a non-PRIA labeling amendment.
02
Gather all relevant documents and previous labeling information.
03
Outline the specific changes that need to be made to the labeling.
04
Complete the non-PRIA amendment form accurately, ensuring all required fields are filled out.
05
Attach the revised labeling draft that reflects the proposed changes.
06
Provide any additional information that may be required to support the amendment request.
07
Review the submission for accuracy and completeness.
08
Submit the amendment to the relevant regulatory authority.

Who needs non-pria labeling amendment?

01
Manufacturers of pesticides who wish to update their product labeling.
02
Companies that have made changes to their formulations which necessitate label updates.
03
Pesticide registrants seeking to clarify or modify claims on their product labels.
04
Industry stakeholders involved in the marketing or distribution of pesticide products.
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A non-PRIA labeling amendment refers to updates or changes made to the labeling of a product that do not qualify under the Pesticide Registration Improvement Act (PRIA) framework.
Any registrant who wishes to make changes to the labeling of their pesticide product must file a non-PRIA labeling amendment if the changes do not fall under the PRIA guidelines.
To fill out a non-PRIA labeling amendment, registrants must complete the appropriate forms provided by the EPA, including details of the labeling changes, and submit them along with the revised labeling.
The purpose of a non-PRIA labeling amendment is to ensure that any significant updates to product labeling are officially documented and approved, maintaining compliance with regulatory requirements.
The information to be reported includes details about the product, a description of the labeling changes, and the rationale for those changes.
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