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  2. Automated dispensing cabinet - Wikipedia

    en.wikipedia.org/wiki/Automated_dispensing_cabinet

    These unit-based medication repositories provide computer-controlled storage, dispensation, tracking, and documentation of medication distribution in the resident care unit. Since automated dispensing cabinets are not located in the pharmacy, they are considered "decentralized" medication distribution systems.

  3. Auxiliary label - Wikipedia

    en.wikipedia.org/wiki/Auxiliary_Label

    An auxiliary label (also called cautionary and advisory label or prescription drug warning label) is a label added on to a dispensed medication package by a pharmacist in addition to the usual prescription label. These labels are intended to provide supplementary information regarding the safe administration, use, and storage of the medication. [1]

  4. Pill organizer - Wikipedia

    en.wikipedia.org/wiki/Pill_organizer

    A pill organiser covering 4 daily doses over one week (labelled in French) Swedish pill organiser, "Dosett". A pill organiser (or pill organizer), pill container, dosette box, pillcase or pillbox is a multicompartment compliance aid for storing scheduled doses of medications.

  5. USP Controlled Room Temperature - Wikipedia

    en.wikipedia.org/wiki/USP_Controlled_Room...

    The USP Controlled Room Temperature is a series of United States Pharmacopeia guidelines for the storage of pharmaceuticals; [1] the relevant omnibus standard is USP 797. [2] [3] Although 100% compliance remains challenging for any given facility, [4] the larger protocol may be regarded as constituting a form of clean room [5] which is included in a suite of best practices.

  6. Vaccine storage - Wikipedia

    en.wikipedia.org/wiki/Vaccine_storage

    Vaccine storage relates to the proper vaccine storage and handling practices from their manufacture to the administration in people. [2] The general standard is the 2–8 °C cold chain for vaccine storage and transportation. This is used for all current US Food and Drug Administration (FDA)-licensed human vaccines and in low and middle-income ...

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  9. Medication package insert - Wikipedia

    en.wikipedia.org/wiki/Medication_package_insert

    In the United States, the Food and Drug Administration (FDA) determines the requirements for patient package inserts. In the United States, the FDA will occasionally issue revisions to previously approved package inserts, in much the same way as an auto manufacturer will issue recalls upon discovering a problem with a certain car.