Dispenser for dispensing pharmaceutical liquid having a housing, a liquid reservoir arranged within the housing, an exit opening through which liquid is discharged into a surrounding atmosphere, an outlet channel connecting the liquid reservoir to the exit opening and having an outlet valve, openable in a pressure-dependent manner or actuatable manually, arranged in the outlet channel. With the valve closed, the outlet channel is subdivided into a first portion upstream of the outlet valve and a second portion downstream of the outlet valve. The housing is of antibacterial design in the region of surfaces which are intended to come into contact with the liquid, wherein it is exclusively surfaces in the region of the second portion and/or of an outer surface of the housing which have this antibacterial design.

A dispensing mechanism includes at least two helical augers having threads, and at least two channels configured to hold the items to be dispensed. The items to be dispensed are received at least partially within the threads of the augers. The dispensing mechanism includes a drive mechanism engaged with the at least two augers and configured to rotate the at least two augers to transport the items to be dispensed, driven by the threads of the augers, to dispense the items from the dispensing mechanism. The dispensing mechanism may include a separable dispenser and cassette.

An apparatus to preserve liquid from a medicine vial may include a vial coupling member forming a vial coupling member cavity and a container forming a cavity. The apparatus may further include a first fluid pathway forming a first lumen that is in fluid communication with the vial coupling member cavity and the cavity and a second fluid pathway forming a second lumen that is in fluid communication with the vial coupling member cavity and the cavity. The vial coupling member cavity, the cavity, the first lumen, and the second lumen may form a sterile environment that is sealed from contaminants in an ambient environment. The apparatus may include a disengaging member configured to permit the container to disengage from the first fluid pathway and the second fluid pathway while permanently sealing at least one of the first lumen or the second lumen.

An unfilled liquid reservoir for use as part of a dispenser for dispensing pharmaceutical or cosmetic liquids, including an outer housing for placing on a dispensing head of the dispenser and a flexible bag arranged within the outer housing for receiving liquid before the dispensing process. The bag has an opening for removing the liquid, and an intermediate region between the outer housing and the bag is connected to a surrounding area by a ventilation opening which passes through a wall of the outer housing. The flexible bag is provided in a stowed storage state in which the inner volume of the bag is maximally 10% of the maximum inner volume of the bag within the outer housing.

A dispensing mechanism includes at least two helical augers having threads, and at least two channels configured to hold the items to be dispensed. The items to be dispensed are received at least partially within the threads of the augers. The dispensing mechanism includes a drive mechanism engaged with the at least two augers and configured to rotate the at least two augers to transport the items to be dispensed, driven by the threads of the augers, to dispense the items from the dispensing mechanism. The dispensing mechanism may include a separable dispenser and cassette.

A self-disinfecting medication vial cap assembly for a medication vial includes a needle-penetrable assembly base configured for attachment to the medication vial; an assembly cap carried by the assembly base, the assembly base and the assembly cap having a cap interior and the assembly cap positional between closed and open positions; a rupturable antiseptic pouch attached to the assembly base and the assembly cap in the cap interior; and an antiseptic contained in the antiseptic pouch. The antiseptic pouch remains intact in the closed position of the assembly cap. The antiseptic pouch ruptures and the antiseptic is discharged onto the assembly base upon movement of the assembly cap from the closed position to the open position.

Provided is an exposure-preventing cap of a novel and simple structure that, by being mounted on a vial, can more reliably inhibit leaking of drug solution to an outside when pulling out and collecting drug solution in a syringe from the vial. An exposure-preventing cap, which is mounted on a mouth of a vial sealed with a rubber stopper, wherein a puncturing hole is formed in a center part of a cap-shaped housing that is attached to a mouth of the vial, and a rubber membrane is arranged at the puncturing hole so as to form an internal space between facing surfaces of the rubber membrane and the rubber stopper. The rubber membrane has a dome shape that is convex facing the rubber stopper.

A food arrangement with at least one receptacle which is filled with a liquid, sterile food; a connector, which is introduced into the receptacle and has a pierced membrane arranged in a filler neck; and a tamper-evident seal, which is connected to the connector and closes the filler neck. A sterile food arrangement is thus made available, without the need for final autoclaving of the entire filled receptacle.

Systems and methods for removing a preservative from a solution, emulsion, or suspension may include an ophthalmic agent, a complexing agent, and a matrix. A method for administering an ophthalmic agent may include: providing a solution, emulsion, or suspension comprising a hydrophobic ophthalmic agent, a preservative, and a complexing agent, wherein the complexing agent is configured to host the hydrophobic ophthalmic agent; and providing a polymeric matrix, wherein the complexing agent is configured to reduce an affinity of the ophthalmic agent for the polymeric matrix and wherein the polymeric matrix is configured to selectively absorb the preservative when the solution, emulsion, or suspension is passed therethrough.

Some fluid coupling devices described herein are configured for use in fluid systems for purposes of providing a sterile connection for drug delivery. In some embodiments, the fluid coupling devices can be implemented as multi-use, sterile fluid coupling devices that are configured to reduce the likelihood of fluid spillage when being disconnected.