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20-2-188
Section 20-2-188 Exceptions to requirements for sale or transfer of chemicals, and to licensing
requirements. (a) The provisions of this article shall not apply to the sale or transfer of
products which include a listed precursor chemical if the product may be sold lawfully with
a prescription or over the counter without a prescription under the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. Section 301 et seq.), or under a rule adopted pursuant to that act.
(b) Notwithstanding any other provision of this article, no person shall be required to obtain
a listed precursor license or permit for the sale, receipt, transfer, manufacture, or possession
of a listed precursor chemical when: (1) Such person is a duly licensed physician, dentist,
veterinarian, podiatrist, or pharmacist, when the sale, receipt, transfer, manufacture, or
possession of such listed precursor chemical is a transaction otherwise lawfully authorized;
(2) A domestic lawful distribution in the usual course of business...
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34-23-157
Section 34-23-157 Components transferred to nonoriginal container; advance product preparation;
labeling. (a) If a component is transferred from the original container to another container,
including, but not limited to, a powder being taken from the original container and stored
in another container, the new container shall be identified with the following information:
(1) Component name and supplier. (2) Lot number and expiration date, if available. (3) Strength
and concentration. (b) Products prepared in anticipation of a prescription prior to receiving
a valid prescription shall be prepared in reasonable amounts. Products shall be labeled or
documentation referenced with all of the following information: (1) A complete list of ingredients
or designated name of the preparation. (2) Preparation date. (3) Beyond use date. (4) Storage
under conditions dictated by composition and stability, including storage in a clean, dry
place or in the refrigerator. (5) Batch or lot number. (c) Upon...
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34-23-9
Section 34-23-9 Purity of drugs dispensed. No person shall compound or sell or offer for sale
or cause to be compounded, sold, or offered for sale any medicine, drug, poison, chemical,
or pharmaceutical preparation that is adulterated. Any one of the above-named substances shall
be deemed to be adulterated if it is sold by a name recognized in the United States Pharmacopoeia
or National Formulary and it differs from the standard of strength, quality, or purity as
determined by the test laid down therein. A product may be of a lesser strength only if the
product is clearly labeled with the actual strength. The board may use product analysis data
from any laboratory that satisfies all of the following qualifications: (1) Is registered
by the Food and Drug Administration. (2) If the product is a legend controlled drug, is licensed
by the Bureau of Narcotics and Dangerous Drugs. (3) Is ISO 17025 certified. (Acts 1966, Ex.
Sess., No. 205, p. 231, §17; Act 2017-422, §1.)...
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34-22-4
Section 34-22-4 Limitation on application of chapter. (a) It is not the intent of this chapter
to prevent any school teacher, welfare worker, state, county, municipality, or other public
board, body, agency, institution, or official from determining in the course of their official
duties the probable need of visual services; provided, that the aforenamed person or agency
does not attempt to examine, diagnose, prescribe, or recommend any particular practitioner
and complies with the provisions of Section 38-1-2. (b) A license to practice optometry shall
not be required for the sale, preparation, or dispensing of eyeglasses or spectacles in a
retail optical dispensary or from a store, shop, or other permanently established place of
business with an optical department on prescription of a duly licensed physician skilled in
diseases of the eyes or a duly licensed optometrist authorized to practice under the laws
of this state. Contact lenses may be sold or dispensed in a retail optical...
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34-23-32
Section 34-23-32 Manufacturer, bottler, packager, repackager, etc., of drugs. (a) Commencing
on August 1, 2017, every manufacturer, bottler, packager, repackager, third party logistic
provider, wholesale drug distributor, private label distributor, outsourcing facility, or
pharmacy business identified in the supply chain of drugs, medicines, chemicals, or poisons
for medicinal purposes shall register annually with the board by application for a permit
on a form furnished by the board and accompanied by a fee to be determined by the board as
follows: (1) The fee shall not be less than five hundred dollars ($500) nor more than two
thousand dollars ($2,000) for a new establishment. (2) The fee shall not be less than two
hundred fifty dollars ($250) nor more than one thousand dollars ($1,000) for a renewal permit.
(3) The fee shall not be less than five hundred dollars ($500) nor more than two thousand
dollars ($2,000) for a permit due to transfer of ownership. (b) A holder of a permit...
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34-23-33
Section 34-23-33 Revocation, suspension, etc., of license or certificate; non-disciplinary
administrative penalty. (a) The board may revoke, suspend, place on probation, or require
remediation for any licensed pharmacist or a holder of a pharmacy intern or extern certificate
for a specified time as determined by the board and take the same or similar action against
the permit to operate any pharmacy in this state, whenever the board finds by a preponderance
of the evidence, or pursuant to a consent decree, that the pharmacist has been guilty of any
of the following acts or offenses: (1) Obtaining a license, permit, or registration from the
board by fraudulent means. (2) Violation of the laws regulating the sale or dispensing of
narcotics, exempt narcotics, or drugs bearing the label "caution, federal law prohibits
dispensing without prescription," or similar wording which causes the drugs to be classified
as prescription legend drugs. (3) Conviction of a felony. A copy of the record of...
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34-23-3
Section 34-23-3 State drug investigators. Each state drug investigator employed by the board
following the passage of this chapter must furnish satisfactory proof to the board that he
or she is a person of good moral character and that in the judgment of the members of the
board he or she has sufficient knowledge of the laws pertaining to the practice of pharmacy
and law enforcement to enable him or her to carry out his or her duties as an investigator
consistent with this chapter. Each state drug investigator employed by the board shall serve
an apprenticeship of a minimum of six months working with and under the supervision of the
Chief Drug Investigator or other investigator designated by the board. Each such investigator,
before entering upon his or her duties, shall post with the board a bond in the amount of
two thousand dollars ($2,000) conditioned upon the faithful performance of his or her duties.
Each state drug investigator shall have the power to inspect the medicines and...
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8-17-80
Section 8-17-80 Definitions. (a) The following words and phrases, when used in this article,
shall have the meanings ascribed to them in this section, except where the context clearly
indicates a different meaning: (1) AVIATION GASOLINE. Motor fuel designed for use in the operation
of aircraft other than jet aircraft, and sold or used for that purpose. (2) BIODIESEL FUEL.
Any motor fuel or mixture of motor fuels that is derived, in whole or in part, from agricultural
products or animal fats, or the wastes of such products or fats, and is advertised as, offered
for sale as, suitable for use as, or used as motor fuel in a diesel engine. (3) BLENDED FUEL.
A mixture composed of gasoline or diesel fuel and any other liquid that can be used as a motor
fuel in a highway vehicle. (4) BOARD. The Alabama Board of Agriculture and Industries. (5)
BRAND. The trade name or other designation under which a particular petroleum product is sold,
offered for sale, or otherwise identified. (6) BULK...
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26-23E-3
Section 26-23E-3 Definitions. As used in this chapter, the following terms shall have the following
meanings: (1) ABORTION. The use or prescription of any instrument, medicine, drug, or any
other substance or device with the intent to terminate the pregnancy of a woman known to be
pregnant with knowledge that the termination by those means will with reasonable likelihood
cause the death of the unborn child. Such use or prescription is not an abortion if done with
the intent to save the life or preserve the health of an unborn child, remove a dead unborn
child, or to deliver the unborn child prematurely in order to preserve the health of both
the mother (pregnant woman) and her unborn child. The term abortion as used in this chapter,
does not include a procedure or act to terminate the pregnancy of a woman with an ectopic
pregnancy, nor does it include the procedure or act to terminate the pregnancy of a woman
when the unborn child has a lethal anomaly. For the purposes of this chapter,...
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27-1-21
Section 27-1-21 Uniformity of limits applied to fulfillment of certain drug prescriptions.
(a) For the purposes of this section, the following words shall have the following meanings:
(1) ENROLLEE. A person enrolled in a health benefit plan. (2) HEALTH BENEFIT PLAN. Any individual
or group plan, policy, or contract for health care services issued, delivered, issued for
delivery, renewed in this state by a health care insurer, health maintenance organization,
accident and sickness insurer, fraternal benefit society, nonprofit hospital service corporation,
nonprofit medical service corporation, health care service plan, or any other person, firm,
corporation, joint venture, or other similar business entity that pays for, purchases, or
furnishes health care services to patients, insureds, or beneficiaries in this state. The
term includes, but is not limited to, entities created pursuant to Article 6 of Chapter 4
of Title 10. The term shall not include any collective bargaining agreement...
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