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County Agricultural Commissioners June 21, 2018 Page 4 The requirements in this box only apply to uses of this product that are covered by the Worker Protection Standard. Do not enter or allow worker entry into treated areas during the restricted entry interval (REI) of 4 hours. PPE required for early entry to treated areas that is permitted under the Worker Protection Standard and that involves contact with anything that has been treated, such as plants, soil, or water, is: • Coveralls • Chemical resistant gloves made of any waterproof material • Shoes plus socks All applicable directions, restrictions, and precautions on the U.S. EPA registered label for INTREPID 2F (EPA Reg. No. 62719-442) and these use directions must be followed. These use directions must be in the possession of the user at the time of pesticide application. The Department of Pesticide Regulation (DPR), Pesticide Registration Branch, shall be immediately informed of any adverse effects resulting from the use of this exemption. Please note: The United States Enviromnental Protection Agency (U.S. EPA) expects concerned growers or grower groups to work toward the registration of use patterns that may be needed on a continuing basis. It will, therefore, be necessary to require applicants wishing to renew emergency exemptions to provide. a progress report on residue tolerance and registration along with request for re -issuance of an emergency exemption. Without substantial progress in pursuing a tolerance and registration for the use in question, it will be difficult to obtain an emergency exemption for another season. The pesticide manufacturer or Western Region IR -4 may be contacted regarding the initiation of a pesticide petition for residue tolerance. A final report must be submitted by the county agricultural commissioner to the Pesticide Registration Branch within 45 days of the expiration date of this exemption. This report must include the following information: a. Amount of product used. b. Units (i.e., acres, trees, cattle) treated. c. Number of applications. d. Estimate of effectiveness. e. Any adverse effects noted.