§329-64  Exceptions.  (a)  The
requirements imposed by sections 329‑62, 329‑63(a), and 329‑67
of this part shall not apply to any of the following:



(1)  Any pharmacist or other authorized person who
sells or furnishes a substance upon the prescription of a physician, dentist,
podiatrist, or veterinarian;



(2)  Any physician, dentist, podiatrist, or
veterinarian who administers or furnishes a substance to patients;



(3)  Any manufacturer or wholesaler licensed by the
State who sells, transfers, or otherwise furnishes a substance to a licensed
pharmacy, physician, dentist, podiatrist, or veterinarian;



(4)  Any sale, transfer, furnishing, or receipt of any
drug that contains pseudoephedrine or norpseudoephedrine that is lawfully sold,
transferred, or furnished over the counter without a prescription pursuant to
the federal Food, Drug, and Cosmetic Act (21 United States Code Sec. 301 et
seq.) or regulations adopted thereunder as long as it complies with the
requirements of sections 329-73, 329-74, and 329-75; and



(5)  Any "dietary supplement" as defined by
the federal Food, Drug, and Cosmetic Act (21 United States Code Sec. 301)
containing ephedrine alkaloids extracted from any species of Ephedra that meets
all of the following criteria:



(A)  It contains, per dosage unit or serving,
not more than twenty-five milligrams of ephedrine alkaloids and its labeling
does not suggest or recommend a total daily intake of more than one
hundred milligrams of ephedrine alkaloids;



(B)  It contains no hydrochloride or sulfate salts
of ephedrine alkaloids; and



(C)  It is packaged with a prominent label
securely affixed to each package that states all of the following:



(i)  The amount in milligrams of ephedrine
alkaloids in a dosage unit or serving;



(ii)  The amount of the dietary supplement that
constitutes a dosage unit or serving; and



(iii)  The maximum recommended dosage of ephedrine
alkaloids for a healthy adult human is not more than one hundred milligrams in
a twenty-four-hour period.



(b)  Notwithstanding the exceptions created by
subsection (a) of this section, any manufacturer, wholesaler, retailer, or
other person who sells, transfers, or otherwise distributes in this State any
list 1 or list 2 chemical, as defined in section 329-61, and who is required to
register with the federal Drug Enforcement Administration as a list I chemical
distributor under federal law (or who registers as a controlled substance
distributor in lieu thereof), shall submit a copy of that registration
application to the department of public safety.  When such application is
granted, the distributor shall file a copy of the federal Drug Enforcement
Administration List I Chemical Registration (or Controlled Substance
Registration) with the department.  The distributor shall also file with the department
a duplicate copy of any reports required under federal law at the same time as
such reports are filed with the federal Drug Enforcement Administration for any
transactions involving list I chemicals that shall be shipped into or otherwise
transferred or distributed in this State.



(c)  The exceptions set forth in subsection (a)
of this section shall not be a defense to any offense as set forth in section
329-65(c) and (d). [L 1990, c 200, pt of §1; am L 1999, c 252, §10; am L 2006,
c 171, §2]