Thickened gelatinous edible alcoholic medicated carrier

Claim 2

In an oral medicating product having an alcohol containing base containing orally ingestible medicating substances compatibly ingestible in the said alcohol containing base, the improvement comprising a taste imparting beverage alcohol having an alcoholic proof strength in the range of about 25-120 as said alcoholic base, medicating substances homogeneously distributed in said beverage alcohol base in concentration to provide a medicating effect in small unit dosage quantities of said medicating product, said product being, gelated with about 3-10% of a gelating agent selected from the group consisting of gelatin, low methoxyl pectin and alkali pectate to provide a substantially solid medicating gel.

Claim 3

The product of claim 1, wherein the pectin is a low methoxyl pectin having less than 10% methoxy groups.

Claim 4

The product of claim 1, wherein the gelating substance is gelatin.

Claim 5

The product of claim 1, wherein the gelating gent is a mixture of gelating agents in said quantity range of low methoxyl pectin having less than 10% methoxyl groups in quantity of about 3 to 7%, and the remainder, at least about 2% methyl cellulose.

Claim 6

The product of claim 1, wherein the medicating substance is a member of the group consisting of high alcohol elixirs, vitamins, organic extracts, cough medicines, pain relievers, medicants, antacids, laxatives, compatibly ingested in an alcohol base as an oral medicant in concentration to be taken orally in small dosage quantities.

Claim 7

The product of claim 1, wherein the medicating substance is a cough syrup compatibly ingested with said beverage to use in small dosage quantities.

Claim 8

The product of claim 1, wherein said beverage alcohol base is a member of the group consisting of liqueurs, cordials, brandies, rums, whiskeys and gins.

Claim 9

In a process of forming an oral medicating product having an alcohol containing base and containing orally ingestible medicating substances, the improvement comprising the steps of adding said medicating substance to a strong taste imparting beverage alcohol in the range of 25-120 proof, adding as said medicating substance one which is compatibly ingestible with said strong beverage alcohol base in concentration therein to provide a medicating effect in small unit dosage quantities of said medicinal product, and adding to said alcohol composition about 3-10% of a gelating agent selected from the group consisting of gelatin, low methoxyl pectin having less than 10% methoxyl groups and alkali pectate and mixing the alcoholic medicinal product at raised temperature above about 100° F. with stirring to dissolve said gelating agent and then cooling to set to a substantially solid medicating gel.

Claim 10

In a process of forming an oral medicating product having an alcohol containing base and containing orally ingestible medicating substances, the improvement comprising the steps of adding said medicating substance to a strong taste imparting beverage alcohol in the range of 25-120 proof, adding as said medicating substance one which is compatibly ingestible with said strong beverage alcohol base in concentration therein to provide a medicating effect in small unit dosage quantities of said medicinal product, and adding to said alcohol composition about 3-10% of a gelating agent selected from the group consisting of gelatin, low methoxyl pectin having less than 10% methoxyl groups and alkali pectate and mixing the alcoholic medicinal product at raised temperature above about 100° F. with stirring to dissolve said gelating agent and then cooling to set to a substantially solid medicating gel.

Claim 11

The method as defined in claim 8, wherein the gelating agent is gelatin.

Claim 12

The method as defined in claim 8, wherein the gelating agent is low methoxyl pectin having less than 10% methoxyl groups and the mixture is heated to a temperature in the range of 100°-140° F. with stirring to dissolve the pectin and then by cooling to set to a substantially solid medicating gel.

Claim 13

The method as defined in claim 8, wherein the gelating agent is alkali pectate and the mixture is heated to a temperature in the range of 100°-140° F. with stirring to dissolve the pectin and then by cooling to set to a substantially solid medicating gel.