[Code of Federal Regulations] [Title 40, Volume 15] [Revised as of July 1, 2003] From the U.S. Government Printing Office via GPO Access [CITE: 40CFR82.120] [Page 435-436] TITLE 40--PROTECTION OF ENVIRONMENT CHAPTER I--ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) PART 82--PROTECTION OF STRATOSPHERIC OZONE--Table of Contents Subpart E--The Labeling of Products Using Ozone-Depleting Substances Sec. 82.120 Petitions. (a) Requirements for procedure and timing. Persons seeking to apply the requirements of this regulation to a product containing a class II substance or a product manufactured with a class I or a class II substance which is not otherwise subject to the requirements, or to temporarily exempt a product manufactured with a class I substance, based on a showing of a lack of currently or potentially available alternatives, from the requirements of this regulation may submit petitions to: Labeling Program Manager, Stratospheric Protection Division, Office of Atmospheric Programs, U.S. Environmental Protection Agency, 6202-J, 1200 Pennsylvania Ave., NW., Washington, DC 20460. Such persons must label their products while such petitions are under review by the Agency. (b) Requirement for adequate data. Any petition submitted under paragraph (a) of this section shall be accompanied by adequate data, as defined in Sec. 82.120(c). If adequate data are not included by the petitioner, the Agency may return the petition and request specific additional information. (c) Adequate data. A petition shall be considered by the Agency to be supported by adequate data if it includes all of the following: (1) A part clearly labeled ``Section I.A.'' which contains the petitioner's full name, company or organization name, address and telephone number, the product that is the subject of the petition, and, in the case of a petition to temporarily exempt a product manufactured with a class I substance from the labeling requirement, the manufacturer or manufacturers of that product. (2) For petitions to temporarily exempt a product manufactured with a class I substance only, a part clearly labeled ``Section I.A.T.'' which states the length of time for which an exemption is requested. (3) A part clearly labeled ``Section I.B.'' which includes the following statement, signed by the petitioner or an authorized representative: ``I certify under penalty of law that I have personally examined and am familiar with the information submitted in this petition and all attached documents, and that, based on my inquiry of those individuals immediately responsible for obtaining the information, I believe that the submitted information is true, accurate, and complete. I am aware that there are significant penalties for submitting false information.'' (4) A part clearly labeled ``Section I.C.'' which fully explains the basis for the petitioner's request that EPA add the labeling requirements to or remove them from the product which is the subject of the petition, based specifically upon the technical facility or laboratory tests, literature, or economic analysis described in paragraphs (c) (5), (6) and (7) of this section. (5) A part clearly labeled ``Section II.A.'' which fully describes any technical facility or laboratory tests used to support the petitioner's claim. (6) A part clearly labeled ``Section II.B.'' which fully explains any values taken from literature or estimated on the basis of known information that are used to support the petitioner's claim. [[Page 436]] (7) A part clearly labeled ``Section II.C.'' which fully explains any economic analysis used to support the petitioner's claim. (d) Criteria for evaluating petitions. Adequate data in support of any petition to the Agency to add a product to the labeling requirement or temporarily remove a product from the labeling requirement will be evaluated based upon a showing of sufficient quality and scope by the petitioner of whether there are or are not substitute products or manufacturing processes for such product: (1) That do not rely on the use of such class I or class II substance; (2) That reduce the overall risk to human health and the environment; and (3) That are currently or potentially available. (e) Procedure for acceptance or denial of petition. (1) If a petition submitted under this section contains adequate data, as defined under paragraph (c) of this section, the Agency shall within 180 days after receiving the complete petition either accept the petition or deny the petition. (2) If the Agency makes a decision to accept a petition to apply the requirements of this regulation to a product containing or manufactured with a class II substance, the Agency will notify the petitioner and publish a proposed rule in the Federal Register to apply the labeling requirements to the product. (3) If the Agency makes a decision to deny a petition to apply the requirements of this regulation to a product containing or manufactured with a class II substance, the Agency will notify the petitioner and publish an explanation of the petition denial in the Federal Register. (4) If the Agency makes a decision to accept a petition to temporarily exempt a product manufactured with a class I substance from the requirements of this regulation, the Agency will notify the petitioner and publish a proposed rule in the Federal Register to temporarily exempt the product from the labeling requirements. Upon notification by the Agency, such manufacturer may immediately cease its labeling process for such exempted products. (5) If the Agency makes a decision to deny a petition to temporarily exempt a product manufactured with a class I substance from the requirements of this regulation, the Agency will notify the petitioner and may, in appropriate circumstances, publish an explanation of the petition denial in the Federal Register.