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This document outlines the reassessment of the tolerance exemptions for the inert ingredient glyceryl tris-12-hydroxystearate, focusing on its use as a pesticide inert ingredient and summarizing its

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What is inert ingredient tolerance reassessment?

Inert ingredient tolerance reassessment is the process of reevaluating and determining the acceptable levels of inert ingredients in pesticide products. Inert ingredients are substances that are not intended to have any pesticidal activity but are included in pesticide formulations to enhance the product's effectiveness or other non-pesticidal purposes.

Who is required to file inert ingredient tolerance reassessment?

The responsibility to file inert ingredient tolerance reassessment lies with pesticide manufacturers or registrants who have products containing inert ingredients. They are required to provide the necessary data and information to support the reassessment.

How to fill out inert ingredient tolerance reassessment?

To fill out inert ingredient tolerance reassessment, pesticide manufacturers or registrants need to gather relevant data and information about the inert ingredients used in their products. This may include chemical composition, toxicity data, and any other information deemed necessary by the regulatory authority. The collected data should then be compiled and submitted according to the specified format and guidelines provided by the regulatory authority.

What is the purpose of inert ingredient tolerance reassessment?

The purpose of inert ingredient tolerance reassessment is to ensure that the levels of inert ingredients in pesticide products do not pose any undue risk to human health or the environment. It is an essential step in the regulatory process to evaluate the safety and effectiveness of pesticide products.

What information must be reported on inert ingredient tolerance reassessment?

Inert ingredient tolerance reassessment requires the reporting of various information related to the inert ingredients used in pesticide products. This may include chemical composition, toxicity data, mode of action, exposure scenarios, and any other relevant data or information required by the regulatory authority.

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