Indiana Code 7.1-7-5-1.1. Requirements for retailers, distributors, and manufacturers
Terms Used In Indiana Code 7.1-7-5-1.1
(c) A retailer shall retain all invoices for e-liquid that the retailer purchases for two (2) years.
(d) A retailer shall not allow the self-service sale for individuals purchasing an e-liquid.
(e) A retailer may not sell an e-liquid that contains more than seventy-five (75) milligrams per milliliter of nicotine.
(f) A manufacturer must have an e-liquid manufacturing permit issued under IC 7.1-7-4.
(g) A distributor that does not have a valid e-liquid manufacturing permit issued under IC 7.1-7-4 must have a valid distributor’s license issued under IC 6-7-2-8.
(h) A distributor shall purchase and distribute e-liquid from an:
(1) Indiana e-liquid manufacturer that has a valid e-liquid manufacturing permit under IC 7.1-7-4; or
(2) Indiana e-liquid distributor that has a valid:
(A) e-liquid manufacturing permit issued under IC 7.1-7-4; or
(B) distributor’s license under IC 6-7-2-8.
(i) A distributor shall retain all invoices to a retailer or from a manufacturer for at least two (2) years.
(j) A manufacturer, distributor, or retailer may not market e-liquid as a modified risk tobacco product, as defined by IC 7.1-7-2-17.5, that has not been designated as a modified risk tobacco product by the federal Food and Drug Administration.
(k) Except as provided in subsection (m), a manufacturer, including a manufacturer of a closed system vapor product, shall annually submit a report to the commission setting forth:
(1) each new product that the manufacturer is producing and is sold in Indiana with a list of the contents and ingredients by volume; and
(2) whether the manufacturer has stopped producing products previously produced and sold in Indiana.
A report under this subsection is confidential, and the commission may not disclose it to another person.
(l) A manufacturer shall annually submit a report to the commission setting forth:
(1) the milligrams per milliliter of nicotine in each product the manufacturer produces; and
(2) the milliliters of each product sold that current year.
A report under this subsection is confidential, and the ATC may not disclose it to another person.
(m) A manufacturer is not required to submit a report described in subsection (k) if the manufacturer submits to the commission a certification, by October 1 of each year, that each of the manufacturer’s vapor products sold in Indiana has been filed with the federal Food and Drug Administration.
As added by P.L.206-2017, SEC.29. Amended by P.L.220-2023, SEC.16.