Uv protectant formulations
US-2024074949-A1 · Mar 7, 2024 · US
US2016338922A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016338922-A1 |
| Application number | US-201615227080-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 3, 2016 |
| Priority date | Aug 7, 2010 |
| Publication date | Nov 24, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Oral compositions and methods of use thereof are provided herein. The oral compositions comprise a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier, and a second component comprising at least one zinc compound, an anti-microbial agent and a pharmaceutically acceptable carrier.
Opening claim text (preview).
1 - 41 . (canceled) 42 . A method for reducing or alleviating dry mouth comprising delivering an oral composition to an oral cavity in a subject, wherein the oral composition comprises: a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier, and a second component comprising at least one zinc compound and a pharmaceutically acceptable carrier. 43 . The method of claim 42 , further comprising mixing the first component and the second component prior to delivering the oral composition to the oral cavity in the subject. 44 . The method of claim 42 , wherein the at least one E h -raising compound is selected from the group consisting of hydrogen peroxide, sodium chlorite, and a fermentable sugar; and the at least one zinc compound is selected from the group consisting of zinc chloride and zinc acetate. 45 . The method of claim 44 , wherein the at least one E h -raising compound is sodium chlorite. 46 . The method of claim 42 , wherein the first component, the second component, or both comprise a humectant selected from the group consisting of glycerin, propylene glycol, hydrogenated glucose syrup, polyethylene glycol, propylene glycol, glycerol, erythritol, xylitol, sorbitol, mannitol, lactitol, and hydrogenated starch hydrolyzates. 47 . The method of claim 46 , wherein the humectant is sorbitol. 48 . The method of claim 42 , wherein the at least one E h -raising compound is selected from the group consisting of an oxyhalogen compound and hydrogen peroxide, and wherein the first composition further comprises a chlorine-containing compound selected from the group consisting of an alkali metal chloride salt, an alkaline earth metal chloride salt, and a combination thereof; and wherein the first component comprises about 0.5% by weight to about 2.5% by weight of the chlorine-containing compound, and the second component comprises about 0.02% by weight to about 1.0% by weight of zinc compound. 49 . A method for treating or ameliorating a canker sore in a subject in need thereof, comprising delivering an oral composition to an oral cavity in the subject, wherein the oral composition comprises: a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier; and a second component comprising at least one zinc compound and a pharmaceutically acceptable carrier. 50 . The method of claim 49 , further comprising mixing the first component and the second component prior to delivering the oral composition to the oral cavity in the subject. 51 . The method of claim 49 , wherein the at least one E h -raising compound is selected from the group consisting of hydrogen peroxide, sodium chlorite, and a fermentable sugar; and the at least one zinc compound is selected from the group consisting of zinc chloride and zinc acetate. 52 . The method of claim 51 , wherein the at least one E h -raising compound is sodium chlorite. 53 . The method of claim 49 , wherein the at least one E h -raising compound is selected from the group consisting of an oxyhalogen compound and hydrogen peroxide, and wherein the first composition further comprises a chlorine-containing compound selected from the group consisting of an alkali metal chloride salt, an alkaline earth metal chloride salt, and a combination thereof; and wherein the first component comprises about 0.5% by weight to about 2.5% by weight of the chlorine-containing compound, and the second component comprises about 0.02% by weight to about 1.0% by weight of zinc compound. 54 . A method for treating or ameliorating tooth decay in a subject in need thereof, comprising delivering an oral composition to an oral cavity in the subject, wherein the oral composition comprises: a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier; and a second component comprising at least one zinc compound and a pharmaceutically acceptable carrier. 55 . The method of claim 54 , further comprising mixing the first component and the second component prior to delivering the oral composition to the oral cavity in the subject. 56 . The method of claim 54 , wherein the at least one E h -raising compound is selected from the group consisting of hydrogen peroxide, sodium chlorite, and a fermentable sugar; and the at least one zinc compound is selected from the group consisting of zinc chloride and zinc acetate. 57 . The method of claim 56 , wherein the at least one E h -raising compound is sodium chlorite. 58 . The method of claim 54 , wherein the at least one E h -raising compound is selected from the group consisting of an oxyhalogen compound and hydrogen peroxide, and wherein the first composition further comprises a chlorine-containing compound selected from the group consisting of an alkali metal chloride salt, an alkaline earth metal chloride salt, and a combination thereof; and wherein the first component comprises about 0.5% by weight to about 2.5% by weight of the chlorine-containing compound, and the second component comprises about 0.02% by weight to about 1.0% by weight of zinc compound. 59 . A method for polishing teeth in a subject in need thereof, comprising delivering an oral composition to an oral cavity in the subject, wherein the oral composition comprises: a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier; and a second component comprising at least one zinc compound and a pharmaceutically acceptable carrier. 60 . A method for treating oral malodor in a non-human animal, comprising delivering an oral composition to an oral cavity of the non-human animal, wherein the oral composition comprises: a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier; and a second component comprising at least one zinc compound and a pharmaceutically acceptable carrier. 61 . An oral composition comprising: a first component comprising at least one E h -raising compound and a pharmaceutically acceptable carrier; a second component comprising at least one zinc compound and a pharmaceutically acceptable carrier; and an anti-inflammatory agent.
Zinc; Compounds thereof · CPC title
Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title
Periodont · CPC title
of vegetable origin · CPC title
Mixing prior to application · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.