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FL CDR Questions and Answers (100% Correct Answers) Already Graded A+

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FL CDR Questions and Answers (100% Correct Answers) Already Graded A+

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FL CDR
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Institution
FL CDR
Course
FL CDR

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Uploaded on
October 20, 2025
Number of pages
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Written in
2025/2026
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FL CDR Questions and Answers (100%
Correct Answers) Already Graded A+
Active pharmaceutical ingredient [ANS:] includes any substance
or mixture of substances intended, represented, or labeled for use
in drug manufacturing that furnishes or is intended to furnish, in a
finished dosage form, any pharmacological activity or other direct
effect in the diagnosis, cure, mitigation, treatment, therapy, or
prevention of disease in humans or other animals, or to affect the
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structure or any function of the body of humans or animals.

"Advertisement" [ANS:] any representation disseminated in any
manner or by any means, other than by labeling, for the purpose
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of inducing, or which is likely to induce, directly or indirectly, the
purchase of drugs, devices, or cosmetics.

"Affiliate"* [ANS:] a business entity that has a relationship with
another business entity in which, directly or indirectly: (a) The
business entity controls, or has the power to control, the other
business entity; or (b) A third party controls, or has the power to
control, both business entities.

"Affiliated party"** (KNOW THIS) [ANS:] means: (a) A director,
officer, trustee, partner, or committee member of a permittee or
applicant or a subsidiary or service corporation of the permittee or
applicant; (b) A person who, directly or indirectly, manages,
controls, or oversees the operation of a permittee or applicant,
regardless of whether such person is a partner, shareholder,
manager, member, officer, director, independent contractor, or
employee of the permittee or applicant; (c) A person who has
filed or is required to file a personal information statement
pursuant to s. 499.012(9) or is required to be identified in an
application for a permit or to renew a permit pursuant to s.

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499.012(8); or (d) The five largest natural shareholders that own at
least 5 percent of the permittee or applicant.

"Applicant" [ANS:] means a person applying for a permit or
certification under this part.

"Certificate of free sale" [ANS:] means a document prepared by
the department which certifies a drug, device, or cosmetic, that is
registered with the department, as one that can be legally sold in
the state.
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"Chain pharmacy warehouse" [ANS:] means a distributor
permitted pursuant to s. 499.01 that maintains a physical location
for prescription drugs that functions solely as a central warehouse
to perform intracompany transfers of such drugs between
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members of an affiliate.

"Closed pharmacy" [ANS:] means a pharmacy that is licensed
under chapter 465 and purchases prescription drugs for use by a
limited patient population and not for wholesale distribution or
sale to the public. The term does not include retail pharmacies.

"Color" [ANS:] includes black, white, and intermediate grays.

"Color additive" [ANS:] means, with the exception of any material
that has been or hereafter is exempt under the federal act, a
material that: (a) Is a dye pigment, or other substance, made by a
process of synthesis or similar artifice, or extracted, isolated, or
otherwise derived, with or without intermediate or final change of
identity from a vegetable, animal, mineral, or other source; or (b)
When added or applied to a drug or cosmetic or to the human
body, or any part thereof, is capable alone, or through reaction
with other substances, of imparting color thereto.

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