A tampon and therapeutic delivery device is disclosed and includes a generally cylindrical applicator tube defining a cartridge within which a tampon is slidably received for ejection through one end of the cartridge. A generally hollow cylindrical plunger member is slidably received within an opposite end of the cartridge for ejecting the tampon therefrom. A cannabinoid-infused disintegrable carrier material is partially embedded in and movably held by the tampon for intravaginal delivery when ejected from the cartridge, whereupon the cannabinoid agent is released into the vagina and absorbed through the vaginal mucosa to provide relief of dysmenorrhea. The cartridge has a plurality of slots to permit pre-lubrication of the tampon, if desired, prior to insertion into the vaginal cavity. The system delivers a higher concentration to the muscle of the uterus, the primary site for the dyskinetic muscle contraction, which is the pathophysiologic cause of dysmenorrhea.

Provided is a tampon applicator having one or more insertion indicators to gauge and/or control the insertion depth of a tampon. The one or more insertion indicators may be located on the tampon applicator barrel, plunger, tampon, removal string, or any combinations thereof. As a result of the one or more insertion indicators, a woman can adjust the insertion depth of the tampon to her body's requirements ensuring leakage protection, comfort, or both.

An intra-uterine device for treating post-partum hemorrhage (PPH) is described, along with an applicator system. In embodiments, the PPH device is comprised of a mesh pouch that is filled with a plurality of sponges. Each sponge is designed to expand upon absorption of fluids, such as blood. The collective expansion of the sponges within the mesh pouch causes the PPH device to expand within a patient's uterus, thus applying pressure to stanch blood flow. The PPH device is loaded into an applicator which is then inserted into a patient, and a corresponding plunger is used to deploy the PPH device. Following completion of treatment, the PPH device may be removed using a removal strand attached to the pouch that is exposed outside of the patient.

A tampon applicator.

A fibrous sheet having a basis weight of between 20 and 1000 g/m.sup.2 that disintegrates in water, has 10% to 70% starch on the basis of the total weight of the dry fibrous sheet. The disintegration time in water, measured in accordance with standard NF Q34-020 applied to a specimen of the sheet of 98 cm.sup.2, is less than 50 seconds. A loss of strength of the sheet measured in accordance with a defined table test corresponds to a loss of strength of a specimen of said sheet forming an angle of at least 85 after having being wetted with water for a duration of 6 seconds, and/or a residual wet strength of the sheet relative to its dry strength, as measured according to a defined ring crush test, is less than 1%. The fibrous sheet may be used for the manufacture of a water disintegrable core in a roll of tissue paper.

A substantially biodegradable and water soluble tampon applicator comprising: a plunger and a barrel, said plunger being of a predetermined length, and having a first end and a second end, said second end being a predetermined distance from said first end, said plunger being substantially cylindrical in shape and having a first diameter at said first end and a second diameter at said second end, wherein said first diameter tapers downwards to said second diameter, proximate said first end, said plunger further comprises a first mating portion, said barrel having a first end and a second end, said second end being a predetermined distance from said first end, said barrel being substantially cylindrical in shape and having a diameter greater than the first diameter of said plunger, proximate said first end of said barrel, there is provided a second mating portion to matingly engage said first mating portion of said plunger to maintain said plunger in relation to said barrel in a first position, proximate said first end of said barrel, adjacent said second mating portion, said barrel further comprises a fingergrip.

A hemostatic device for treatment of a gunshot wound includes a barrel, which has a first end that is open, and a plunger. The barrel is arcuate adjacent to a second end to define a tip section. A clotting medium and a gauze are positioned in the barrel proximate to the tip section and between the clotting medium and the first end, respectively. A plurality of slits that is positioned in the tip section defines a plurality of petals, which comprise plastic and are resiliently deformable. The plunger, which has a head that is sealably positioned in the barrel adjacent to the first end, is configured to be pushed into the barrel to apply pressure to the gauze and the clotting medium so that the petals separate. The clotting medium and the gauze are sequentially expelled from the barrel into a wound to induce clotting and to pack the wound.

A medical delivery device for treating a tunneling wound includes an outer sleeve, a plunger, and a hollow tube extending through an opening in the plunger. The plunger is configured to deliver a wound treatment material from an inner cavity of the outer sleeve, through a cavity opening on the outer sleeve, and into the tunneling wound. The hollow tube is configured to deliver a fluid to the wound treatment material after insertion into the tunneling wound. In some embodiments, the medical delivery device may further include a flap disposed on the outer sleeve. The flap may be reconfigurable between a closed position in which the flap is configured to shield the cavity opening, and an open position in which the flap is configured to allow the wound treatment material to be ejected through the cavity opening.

Provided is a tampon applicator having one or more insertion indicators to gauge and/or control the insertion depth of a tampon. The one or more insertion indicators may be located on the tampon applicator barrel, plunger, tampon, removal string, or any combinations thereof. As a result of the one or more insertion indicators, a woman can adjust the insertion depth of the tampon to her body's requirements ensuring leakage protection, comfort, or both.

Disclosed is a tampon applicator package assembly having a tampon applicator and a cap having a closed end and an open end. The tampon applicator has a barrel for housing a pledget and a plunger. The plunger has an end portion that is a cap cover that connects to a remainder of the plunger and mates with the cap at the open end to provide a seal with the cap that completely encloses the tampon applicator in the cap. Also disclosed is an assembly having a tampon applicator, a cap having both a closed end and open end, and a cap cover for covering the open end of the cap. When the cap cover is placed on the open end, the open end is sealed and the tampon applicator is completely enclosed in the cap.