One pouch for storage of multiple components of a mixture is described with a first compartment and a second compartment. At least one channel is defined between the first compartment and the second compartment and at least one seal is installed within the channel. Method of use the pouch includes: locating the channel; breaking the seal; and mixing the contents in the first and second compartment.

A multiple chamber container forming and filling method includes (i) forming at least one strong seal around a periphery of first and second sheets so as to leave an opening between the first and second sheets; (ii) forming a temporary peel seal across the opening; (iii) forming a mixing peel seal between the first and second sheets so as to separate a diluent chamber from a powdered drug chamber; (iv) adding diluent to the diluent chamber; (v) sterilizing the multiple chamber container including the diluent; (vi) opening the temporary peel seal in an aseptic environment; (vii) adding powdered drug to the powdered drug chamber through the opening; and (viii) strong sealing the opening so as to be closed.

A dispenser actuator assembly (100) for actuating a dispenser (10) has a base member (102) operably connected to an actuator assembly (104). The dispenser (10) is in the form of a glass ampoule assembly (10) having a rupturable glass ampoule (12) containing a flowable material (M). The glass ampoule (12) is contained within an outer container (14). The glass ampoule assembly (10) has an applicator (16) positioned in the outer container (14). The dispenser actuator assembly (100) has the base member (102) that is configured to mount on the outer container (14). The actuator assembly (104) has a first actuator arm (132a) and a second actuator arm (132b) each pivotally connected to the base member (102). The first actuator arm (132a) has a first protrusion (150a) depending therefrom and the second actuator arm (132b) has a second protrusion (150b) depending therefrom. The first actuator arm (132a) and the second actuator arm (132b) are pivotable such that the first protrusion (150a) and the second protrusion (150b) engage the outer container (14) to rupture the glass ampoule (12).

Packaging material is provided. The packaging material can include at least one web layer having a surface that includes first and second regions. When corresponding first regions are overlaid with each other and corresponding second regions are overlaid with each other, the overlaid first and second regions can cooperatively surround a cavity. The packaging material further can include a first sealing material disposed in the first region and configured to seal together the corresponding first regions upon application of first conditions to the first sealing material, and a second sealing material disposed in the second region and configured to seal together the corresponding second regions upon application of second conditions to the second sealing material. The second sealing material can be configured such that the first conditions applied to the second sealing material are insufficient to cause the second sealing material to seal.

A retortable package includes a body defining a perimeter and a peripheral seal formed along the perimeter of the body. The peripheral seal includes at least one peripheral self-venting region and at least one peripheral non-venting region. The retortable package further includes an intermediate seal formed within the perimeter of the body and contiguous with the peripheral seal. The intermediate seal divides the body into two compartments. The compartments receive respective products therein. Upon heating of the products, the intermediate seal ruptures before the at least one peripheral self-venting region ruptures. Further, the at least one peripheral self-venting region ruptures before the at least one peripheral non-venting region ruptures.

A fluid treatment kit comprises a flexible plastic container defining a first compartment and a second compartment. The first compartment contains a treating fluid. The second compartment contains at least one applicator. A breakable seal is disposed between the first compartment and the second compartment. The breakable seal is breakable to allow the treating fluid to flow into the second compartment and contact with the applicator. The applicator comprises liquid-absorbing materials and absorbs the treating fluid. The user then opens the flexible plastic container to remove the applicator and uses the applicator for the treatment of the pet.

A dispenser actuator assembly (100) for actuating a dispenser (10) is disclosed. The dispenser (10) is in the form of a glass ampoule assembly (10) having a rupturable glass ampoule (12) containing a flowable material (M). The glass ampoule (12) is contained within an outer container (14) wherein the outer container (14) has a first open end (22) and a second closed end (24). The glass ampoule assembly (10) has an applicator (16) positioned in the first open end (22). The dispenser actuator assembly (100) has a base member (102) configured to mount on the outer container (14). The dispenser actuator assembly (100) also has an actuator assembly (104) operably connected to the base member (102) wherein the actuator assembly (104) has a first actuator arm (132a) and a second actuator arm (132b) each pivotally connected to the base member (102). The first actuator arm (132a) and the second actuator arm (132b) extend from the base member (102) in generally opposed relation defining a first position. The first actuator arm (132a) has a first protrusion (150a) depending therefrom and the second actuator arm (132b) has a second protrusion (150b) depending therefrom. The first actuator arm (132a) and the second actuator arm (132b) are pivotable from the first position towards one another to a second position that is configured such that the first protrusion (150a) engages the outer container (14) and the second protrusion (150b) engages the outer container (14) to rupture the glass ampoule (12) wherein the flowable material (M) is configured to be dispensed from the glass ampoule assembly (10). The dispenser (10) can also be a plastic ampoule assembly (10) having a fracturable membrane (52) having a weld seam (56).

A bagger device is provided. The bagger device can include a bag handler configured to handle packaging material configured to define a bag that has first and second walls enclosing an interior cavity configured to contain an object therein for shipping, the first wall including an expansion material that has an expandable configuration and that is expandable to an expanded configuration for providing padding to the first wall to protect the object contained within the interior cavity. The bagger device can further include an expansion device configured to apply expanding conditions to the packaging material, the expanding conditions configured to cause the expandable material to expand from the expandable configuration to the expanded configuration.

Packaging material is provided. The packaging material can include at least one web layer having a surface that includes first and second regions. When corresponding first regions are overlaid with each other and corresponding second regions are overlaid with each other, the overlaid first and second regions can cooperatively surround a cavity. The packaging material further can include a first sealing material disposed in the first region and configured to seal together the corresponding first regions upon application of first conditions to the first sealing material, and a second sealing material disposed in the second region and configured to seal together the corresponding second regions upon application of second conditions to the second sealing material. The second sealing material can be configured such that the first conditions applied to the second sealing material are insufficient to cause the second sealing material to seal.

An extended duration anesthetic includes a short duration local anesthetic in a dilute solution and a long duration local anesthetic. The long duration local anesthetic is maintained in a powdered form until the time of administration. Premeasured quantities of the dilute solution and powdered long duration local anesthetic in a kit allow for quick preparation of a solution with desired concentrations of both short duration local anesthetic and long duration local anesthetic at the time of administration.