The invention describes a blister packaging system, and method of making the system, capable of establishing and maintaining arid and anaerobic conditions for packaging pharmaceutical products that are sensitive to oxygen and/or moisture. The blister packaging system encompasses, for example, a scaffold of several interconnected cavities intended for product and one or more reservoirs comprising an oxygen scavenger and/or a desiccant. Furthermore, the concentration of the components is maintained at a level that prevents establishment of equilibrium conditions.

A packaged oral care implement (1000) and method of opening the same. In one embodiment, the package (2000) has a first panel (100) that includes a pre-weakened line (103) including at least two portions (103A, 103B) of differing non-zero shear strengths so that an easy as open location (106) is provided.

The present invention relates to a blister pack that comprises a base laminate with a sealing layer and a lid laminate with a sealing layer, the base laminate having at least one cavity housing a product. The base laminate and the lid laminate are directly sealed to each other via their identical sealing layers whereby the seal comprises two different sealing subzones, a first sealing subzone providing a permanent seal and a second sealing subzone providing a peelable seal.

The invention is directed to a confection package comprising of a plastic mould product (1) comprising a horizontal planar surface (5), a first recess space (2) for a confection, a second recess space (3) for one end of a handle (6), a planar cover sheet (7), a volume of a freezable or frozen confection (8) as present within the first recess space (2), and a handle (6). An intermediate part (11) of the handle (6) is positioned below planar cover sheet (7) and positioned in a third recess space (20) provided with a base surface (15) on which the intermediate part (11) of the handle rests. The base surface (15) is provided with one or more grooves (22).

A sample cosmetic product (1) having an applicator including a shell (7), incorporating a first portion (13) with a first cavity (10) and a second portion (15) with a second cavity (13) connected together so as to enable the reception of an applicator. A cover (8) is positioned on the shell to cover the first cavity and the second cavity, the cover welded around the first cavity on the first portion of the shell forming a first weld (26), and around the second cavity of the second portion of the shell forming a second weld (27). The first weld is configured to be dewelded by peeling away the cover to enable the opening of the first cavity. The packaging has a reinforcing mechanism separating the first portion and the second portion, the reinforcing mechanism is configured to prevent the dewelding of the second weld.

Sterile transport, storage, and operation of fluid collection tubes in platelet-rich fibrin and platelet-rich plasma procedures. Sterile sample tube packages comprise a tray having a recessed cavity formed therein, one or more fluid collection tubes, and a cover. Each cavity houses a tube. A practitioner accesses a tube without contaminating the remaining tubes.

Sample cosmetic product (1) having an applicator comprising: a shell (7), incorporating a first portion (13) comprising a first cavity (10), and a second portion (15) comprising a second cavity (13) connected together so as to enable the reception of an applicator, a cover (8) positioned on the shell so as to cover the first cavity and the second cavity, the cover being welded around the first cavity on the first portion of the shell forming a first weld (26), and around the second cavity of the second portion of the shell forming a second weld (27), the first weld being intended to be dewelded by peeling away the cover in order to enable the opening of the first cavity,
the packaging comprising reinforcing means separating the first portion and the second portion, the reinforcing means being intended to prevent the dewelding of the second weld.

The method for producing blister packs for medicinal products comprises the steps of forming blister pockets in a bottom film, wherein each blister pocket has an at least two-level shape with a first recess and a second, lower recess, filling the second recesses of the blister pockets with the medicinal products, placing a strip of active material in the first recess of each blister pocket above the medicinal product, wherein the strip of active material rests on at least one support surface of the first recess next to the second recess, sealing a lidding film to webs of the bottom film arranged around the blister pockets and simultaneously to the strips of active material, thus forming a sealed blister web, and stamping out individual blister packs from the blister web.

The multi-chambered well dosage form and device disclosed herein can be single or multi dose capable for administration of pharmaceuticals of a range of particle sizes. The present dosage devices and systems provide for improved efficiency and patient ease of use owing to its compact size and simple design, low cost, and consistent, contamination free dosing of dry powder medicaments or other agents. The present disclosure provides a multi-chambered dosage form containing dry powder medical composition containing chamber well with an internal piercing device and one or more adjacent gas-filled chamber wells to aid the dispense of the powder contents to the user and in certain embodiments, without the requirement of an external energy sources common with active devices known in the art. Said methods, systems and devices provide increased ejection fraction and hence greater efficiency of drug delivery above that as provided by current devices.

A packaging comprising a plastic foil molded part and a cover foil, wherein the plastic foil molded part defines the front side of the packaging and the cover foil defines the back side of the packaging and the cover foil is based on a carrier substrate provided with a semitransparent function layer, wherein the semitransparent function layer is constituted such that the cover foil has a first, visually recognizable color upon viewing in incident light and has a second, visually recognizable color upon viewing in transmitted light.