SENATE FLOOR VERSION - HB2511 SFLR Page 1 (Bold face denotes Committee Amendments) 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 SENATE FLOOR VERSION April 5, 2021 ENGROSSED HOUSE BILL NO. 2511 By: Kannady of the House and Howard of the Senate An Act relating to tobacco and vapor products; requiring vapor product manufacturers to make a certain attestation to the Alcoholic Beverage Laws Enforcement Commission; providing for contents of the attestation; requiring notification of material changes to the attestation; requiring the ABLE Commission to develop, publish, and maintain a certain directory; prohibiting certain acts; providing for codification; and p roviding an effective date. BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA: SECTION 1. NEW LAW A new section of law to be codified in the Oklahoma Statutes as Section 1-229.35 of Title 63, unless there is created a duplica tion in numbering, reads as follows: A. Beginning July 1, 2022, every manufacturer of a vapor product that is sold or intended to be sold in this state, whether directly or through a distributor, reta iler or similar intermediary or intermediaries, shall execute and deliver an attestation under penalty of perjury to the Oklahoma Alcoholic Beverage Laws SENATE FLOOR VERSION - HB2511 SFLR Page 2 (Bold face denotes Committee Amendments) 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Enforcement (ABLE) Commission certifying that, as of the date of such attestation: 1. The vapor product was available for purchase in the United States as of August 8, 2016, and the manufacturer has applied for a marketing order for the vapor product by submitting a Premarket Tobacco Product Application on or before September 9, 2020, to the United States Food and Drug Administration (FDA); or 2. The manufacturer has received a marketing order or other authorization for the vapor product from the FDA pursuant to Section 387j of Title 21 of the United States Code. B. The manufacturer shall notify the ABL E Commission within thirty (30) days of any material ch ange to the attestation including whether the FDA has issued or not issued a market order or other authorization or has ordered the manufacturer to remove the vapor product, either temporarily or perm anently, from the United States market. C. The ABLE Commission shall develop a directory listing all of the manufacturers that have provided attestations that comply with subsection A of this section and all vapor products that are listed in such attestations. The ABLE Commission shall: 1. Make the director y available for public inspection on its website on or before October 1, 2022; and SENATE FLOOR VERSION - HB2511 SFLR Page 3 (Bold face denotes Committee Amendments) 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 2. Update the directory as necessary to correct mistakes and to add or remove manufacturers or vapor products to main tain the directory in conformity with the requirements of this section. D. It shall be unlawful for any person, directly or indirectly, to knowingly manufacture, distribute, sell, barter or furnish in this state any vapor product that is not included in the directory. SECTION 2. This act shall become effective November 1, 2021. COMMITTEE REPORT BY: COMMITTEE ON HEALTH AND HUMAN SERVICES April 5, 2021 - DO PASS