Colostrum Composition Enriched in Anti-Endotoxin Antibodies
US-2015335709-A1 · Nov 26, 2015 · US
US9445970B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9445970-B2 |
| Application number | US-201414228602-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 28, 2014 |
| Priority date | Dec 17, 2010 |
| Publication date | Sep 20, 2016 |
| Grant date | Sep 20, 2016 |
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A daily blister card housing a unit dose includes a back side and a front side opposite the back side. The front side includes a manufacturer indicator visible on the front side. A face has an outer periphery and a total planar area bounded by the outer periphery. One or more blisters extend outwardly at the face that contains at least three unit doses that are visible from outside the one or more blisters. Each of the one or more blisters includes a shoulder contacting a cavity backing surface and a projected cavity area bounded by the shoulder that is projected onto the cavity backing surface. A total projected cavity area of the one or more blisters is no more than about 45 percent of the total planar area bounded by the outer periphery.
Opening claim text (preview).
What is claimed is: 1. A conveniently portable daily blister card comprising: a. a front side including: i. a face having a width, a right side edge, a left side edge, a top edge, and an outer periphery; ii. at least three and no more than five blisters extending outwardly at the face wherein each blister contains a unit dose; iii. a primary manufacturer indicia area comprising a manufacturer indicator visible on the front side and the primary manufacturer indicia area does not comprise blisters; b. a back side opposite the front side including: i. regulatory information wherein sufficient regulatory information remains on the back side when each unit dose is removed from the blisters through the back side of the card. 2. The blister card of claim 1 wherein the regulatory information is selected from the group consisting of dosing instructions, lot number, expiration date, opening instructions, and combinations thereof. 3. The blister card of claim 1 wherein the primary manufacturer indicia area extends continuously along the width between the left side edge and the right side edge. 4. The blister card of claim 1 wherein one unit dose is different than the other unit doses. 5. The blister card of claim 4 wherein the unit dose that is different is adapted for consumption at night. 6. The blister card of claim 4 wherein the unit dose that is different is a different color. 7. The blister card of claim 1 wherein at least two doses are adapted for consumption during the day. 8. The blister card of claim 1 wherein the unit doses comprise one or more actives useful to treat a respiratory condition. 9. The blister card of claim 1 wherein the blister card comprises a total planar area from about 50 cm 2 to about 120 cm 2 . 10. The blister card of claim 1 wherein the primary manufacturer indicia area is adjacent to the top edge. 11. The blister card of claim 1 , wherein the unit doses are arranged in a sequentially directional dosing arrangement. 12. A conveniently portable daily blister card comprising: a. a front side including: i. a face having a width, a right side edge, a left side edge, a top edge, and an outer periphery; ii. at least three and no more than five blisters extending outwardly at the face wherein each blister contains a unit dose and wherein each blister includes a shoulder contacting a cavity backing surface and a projected cavity area bounded by the shoulder that is projected onto the cavity backing surface; iii. a primary manufacturer indicia area; b. a back side opposite the front side including: i. at least one unit dose instructional subarea associated with each unit dose wherein each instructional subarea includes regulatory information selected from the group consisting of dosing instructions, lot number, expiration date, opening instructions, and combinations thereof and wherein sufficient regulatory information remains on the back side when each unit dose is removed from the blisters through the back side of the card. 13. The blister card of claim 12 wherein the projected cavity area of the blisters is no more than 45 percent of the total planar area bounded by the outer periphery. 14. The blister card of claim 12 wherein the primary manufacturer indicia area extends continuously along the width between the left side edge and the right side edge. 15. The blister card of claim 12 further comprising a primary unit dose indicia area wherein the primary unit dose indicia area is adjacent to the blisters and extends continuously along the width between the left side edge and the right side edge and wherein the primary unit dose indicia area is opposite and associated with the unit dose instructional subareas. 16. The blister card of claim 12 further comprising a primary unit dose indicia area wherein the primary unit dose indicia area surrounds the blisters and wherein the primary unit dose indicia area is opposite and associated with the unit dose instructional subareas. 17. The blister card of claim 12 wherein the front side further comprises a unit dose indicia area comprising two or more instructional indicators that indicates a period of day that the unit is to be consumed.
Decoration means, markings, information elements, contents indicators · CPC title
Printed labels · CPC title
Colour codes · CPC title
and forming several compartments · CPC title
Blister-type containers (blisters in general B65D75/36) · CPC title
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