A save-and-draw capping system may be snapped or otherwise attached/connected to the top of a liquid medicine bottle having a rubber surface that may be punctured using a syringe to draw medicine. Using the save-and-draw capping system, the rubber surface may be sealed after it has been punctured. A secondary seal may be used to apply pressure to the cap of the liquid medicine bottle. A draw attachment, such as a draw needle, may be attached to the save-and-draw cap so that a hose may be connected to the liquid medicine bottle when multiple injections are needed. The save-and-draw capping system may be removed from one liquid medicine bottle to be used on another liquid medicine bottle.

An antifreeze cartridge includes a container containing an antifreeze agent, and a sealing film on the container. A connecting structure is configured and intended to be connected by force fit or form fit to a complementary receiver of an antifreeze inlet of a motor vehicle. The container has a handling portion which is configured and intended to allow the manual connection of the connecting structure to the complementary receiver of the antifreeze inlet. The sealing film is configured and intended to be perforated by a hollow perforation element of the antifreeze inlet so that the antifreeze agent contained in the container can be supplied to a frost-protection system of the motor vehicle through the hollow perforation element. A motor vehicle has an antifreeze inlet wherein the antifreeze inlet is accessible from the outside of an engine bay of the motor vehicle without opening a hood of the motor vehicle.

A cap assembly includes an access member configured for attachment to a reservoir. The access member includes a first port that enables needleless extraction of contents from the reservoir, and at least one second port that enables needled extraction of the contents from the reservoir. The cap assembly further includes a valve member positioned in or configured to be positioned in the access member to i) enable needleless extraction of the contents of the reservoir through the first port when the first port is attached to a needless extraction device, ii) enable needled extraction of the contents through the at least one second port, and iii) seal the contents of the reservoir at the first port and at the at least one second port prior to and subsequent to the needleless or needled extraction.

A vial blinding assembly includes a vial having a bottle with a constricted neck and an annular shoulder that inwardly extends; a stopper disposed on an opening of the bottle and having a septum with a top surface; and a retainer securing the stopper to the bottle. A tubular blinding shell encircles a compartment that extends between a first end with an inlet opening and an opposing second end with an access opening. A floor plug is secured to the first end of the blinding shell. The vial is disposed within compartment of the blinding shell with the vial being supported by the floor plug and the neck passing through the access opening so that the top surface of the septum is disposed outside of the compartment of the blinding shell, the shoulder of the vial having an outside diameter larger than a diameter of the access opening.

A bubble manufacturing container 20 of the present invention includes: a container body 21 having an opening portion; and a rubber stopper 221 provided on the opening portion of the container body 21. The rubber stopper 221 is constituted so that the bubbles 1 of an inside of the container body 21 are able to be taken by piercing an injection needle. It is preferred that the bubble manufacturing container 20 has a fastening portion 222 provided on the rubber stopper 221, having an opening and sealing the container body 21 with the rubber stopper 221. Furthermore, it is preferred that the container body 21 mounts a weight portion.

A clean, sterile fingertip mist of simulated saliva of appropriate droplet size and quantity is provided to allow consumers to easily moisten their fingertips to open produce bags, to count money, separate papers and for other applications where moist fingertips are useful. The simulated saliva provided substitutes for natural saliva to avoid spread of germs such as virus, bacterium, bacillus and other microbes and microorganisms, and other undesirables found in natural human saliva. A misting apparatus is provided, being tailored for delivery of a fine range, having distributed, but limited, quantity of droplets of sterile simulated saliva. This invention avoids consumers passing germs by using their own germ laden saliva to moisten fingertips then open produce bags, county money, separate papers and the like. In one embodiment, a method of layer separation by use specific sterile simulated saliva and mist dispenser therefor are provided in lieu of actions such as (i) licking fingertips, (ii) applying oily lotions or thick globs of hand sanitizer (iii) wearing gloves or (iv) intense, repetitive rubbing for friction separation.

A tubular locking body of a tamper evident plastic closure for necked vials for holding a plug in a mouth of a vial includes a retaining member for retaining the plug, a central opening being formed in the retaining member for providing access to the inside of the vial via the plug. The cap includes a disc-shaped cover and a coupling portion, for coupling the cap with the tubular locking body by positive-fit engagement. The coupling portion includes at least one frangible portion each configured such that at least one indicator member remains as a tamper evidence at a rim of the central opening of the tubular locking body after removal of the cap from the distal end of the tubular locking body by irreversibly breaking the annular frangible portion for providing access to the inside of the vial via the plug.

A needleless syringe connector cap to be provided to a container having an aperture at its top, said cap comprising an elastically deformable plastic valve body. Said valve body comprises a first and second passage, each passage extending through the valve body. Both passages comprise a cross-slit valve in the extreme lower end of said passage, embodied as an aeration valve. The first passage is adapted to receive a first tapered syringe tip and the second passage is adapted to receive a second tapered syringe tip, wherein when fluid is withdrawn from a container to which the cap is provided through the first (second) passage using a first (second) tapered syringe tip to which said first (second) passage is adapted, the second (first) cross-slit valve opens in response to an under pressure in said container resulting from said withdrawal, so as to aerate said container.

A sealed pharmaceutical container includes a shoulder, a neck extending from the shoulder, and a flange extending from the neck. The flange includes an inclined sealing surface defining an opening in the sealed pharmaceutical container. The sealed pharmaceutical container also includes a sealing assembly including a stopper extending over the sealing surface of the flange and a cap securing the stopper to the flange. The stopper has a glass transition temperature (T.sub.g) that is greater than or equal to 70 C. and less than or equal to 45 C. The sealing assembly maintains a helium leakage rate of the sealed pharmaceutical container of less than or equal to 1.410.sup.6 cm.sup.3/s as the sealed pharmaceutical container is cooled to a temperature of less than or equal to 45 C.

A container has an at least partially filled container body and at least one cap part (10). The cap part has at least one sealing part (16) that, for removal of the container contents, can be penetrated by a hollow-spike-shaped insertion part (22) from the outside, with a predeterminable actuating force, in an introduction direction. The insertion part can be removed from the container again, with a predeterminable pull-out force, in an oppositely directed pull-out direction. A device (16, 18) makes it difficult for the insertion part (22) to be removed with the pull-out force being increased such that unintentional removal of the insertion part (22) is at least made difficult.