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Greenbaum, \"The Story of Allantoin,\" Am. K. Pharm. 112:205-216 (1940).","npl_type":"a","external_id":[],"lens_id":[],"sequence":72,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":2,"text":"M.A. Lesser, Allantoin,: Drug Cosmet. Ind. 42:451-456, 469 (1938).","npl_type":"a","external_id":[],"lens_id":[],"sequence":73,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":3,"text":"I.I. Lubowe & S.B. Mecca, \"Allantoin and Aluminum Derivatives in Dermatological Applications,\" Drug Cosmet. Ind. 84:36, 37, 117 (1959).","npl_type":"a","external_id":[],"lens_id":[],"sequence":74,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":4,"text":"S.B. Mecca, \"Allantoin and the Newer Aluminum Allantoinates,\" Proc. Scient. Sect. Toilet Goods Assoc. No. 31:1-6 (1959).","npl_type":"a","external_id":[],"lens_id":[],"sequence":75,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":5,"text":"S.B. Mecca, \"The Function and Applicability of the Allantoinates,\" Proc. Scient. Sect. Toilet Goods Assoc. No. 39:7-15 (1963).","npl_type":"a","external_id":[],"lens_id":[],"sequence":76,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":6,"text":"P. LeVan et al., \"The Use of Silicones in Dermatology,\" Calif. Med. 8:210-213 (1954).","npl_type":"a","external_id":["13190431","pmc1532133"],"record_lens_id":"154-041-452-373-488","lens_id":["165-914-180-664-239","154-041-452-373-488"],"sequence":77,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":7,"text":"R. Cahen & A. Pessonnier, \"Etude Pharmacologique de L'Allantoïnate de Dihydroxyaluminium et de L'Allantoïnate de Chlorhydroxy-aluminium. I.-Toxicité,\" Ann. Pharm. Franç. 20:623-636 (1962) (in French), discloses the physical and chemical properties and the toxicity of dihydroxyaluminum allantoinate and chlorhydroxyaluminum allantoinate. The compounds were observed to have no toxicity.","npl_type":"a","external_id":[],"lens_id":[],"sequence":78,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":8,"text":"R. Cahen & J.-F. Clement, \"Etude Pharmacologique de L'Allantoïnate de Dihydroxyaluminium et de L'Allantoïnate de Chlorhydroxy-aluminium. II.-Etude de l'Activité Gastrique,\" Ann. Pharm. Franç. 20:693-703 (1962) (in French), discloses the activity of dihydroxyaluminum allantoinate and chlorhydroxyaluminum allantoinate on gastric activity. The compounds were found to have acid-neutralizing and buffering activity and to diminish gastric acidity.","npl_type":"a","external_id":[],"lens_id":[],"sequence":79,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":9,"text":"R. Cahen & A. Pessonnier, \"Etude Pharmacologiqie de L'Allantoïnate de Dihydroxyaluminium et de L'Allantoïnate de Chlorhydroxyaluminium. III.-Effet Anti-ulcéreux,\" Ann. Pharm. Franç. 20:704-713 (1962) (in French), discloses the anti-ulcer activity of the compounds dihydroxyaluminum allantoinate and chlorhydroxyaluminum allantoinate. The compounds were found to have anti-ulcer activity in rats and guinea pigs comparable to compounds such as aluminum hydrate and bismuch subnitrate.","npl_type":"a","external_id":[],"lens_id":[],"sequence":80,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":10,"text":"R. Cahen & A. Pessonnier, \"Etude Pharmacologique de L'Allantoënate de Dihydroxyaluminium et de L'Allantoïnate de Chlorhydroxyaluminium. IV.-Effet sur l'Ulcère Médicamenteux Expérimental,\" Ann. Pharm. Franç. 21:215-222 (1963) (in French), discloses the effect of the compounds dihydroxyaluminum allantoinate and chlorhydroxyaluminum allantoinate on ulcers produced in the rat administration of phenylbutazone or reserpine. The compounds were found to have activity against such ulcers.","npl_type":"a","external_id":[],"lens_id":[],"sequence":81,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":11,"text":"C. Debray et al., \"Etude de Dèrivés Allantoïniques de l'Aluminium dans la Thérapeutique des Affections Gastro-duodénales,\" Presse Méd. 70:2643 (1962) (in French) discloses the activity of the compounds dihydroxyaluminum allantoinate and chlorhydroxyaluminum allantoinate administered in a complex with a polymer of polyoxyethylene and polyoxypropanediol, methlhomatropine bromide, and calcium carbonate on gastrointestinal conditions. The complex was said to be effective against duodenal ulcer and effective in protecting the gastric mucosa.","npl_type":"a","external_id":[],"lens_id":[],"sequence":82,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":12,"text":"Japanese patent publication No. JP 58140013 A Daiichi Seiyaku Co., published Aug. 19, 1983.","npl_type":"a","external_id":[],"lens_id":[],"sequence":83,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":13,"text":"Publication-product information insert for Alphosyl Cream and Alphosyl Lotion, G.D. Searle (South Africa), Apr. 24, 1975.","npl_type":"a","external_id":[],"lens_id":[],"sequence":84,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":14,"text":"Publication-product information insert for Clearasil Medicated Facial Cleanser, Procter & Gamble (South Africa) Jan. 31, 1994.","npl_type":"a","external_id":[],"lens_id":[],"sequence":85,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":15,"text":"Publication-product information insert fo Arola Rosebaum, Supramed Limited, Jan. 12, 1986.","npl_type":"a","external_id":[],"lens_id":[],"sequence":86,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":16,"text":"Abstract of a publication-M.Cajkovac et al., \"Influence of Emulsoid Vehicle on the Release and Activity of Allantoin,\" Pharmazie 47: 39-43 (1992) (abstract only).","npl_type":"a","external_id":["1608983"],"record_lens_id":"031-345-559-270-262","lens_id":["089-325-003-962-382","031-345-559-270-262"],"sequence":87,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":17,"text":"Abstract of a publication-M. Maragakis et al., \"Possibilities of Scar Treatment After Thoracic Surgery,\" Drugs Under Exp. & Clin. Res. 21: P199-206 (1995) (abstract only).","npl_type":"a","external_id":["8846750"],"record_lens_id":"156-793-208-117-567","lens_id":["177-462-485-320-876","156-793-208-117-567"],"sequence":88,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":18,"text":"Publication-product information insert for Alphosyl, undated.","npl_type":"a","external_id":[],"lens_id":[],"sequence":89,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":19,"text":"Abstract of a publication-G. Stinco et al., \"Seborrheic Dermatitis Treated with Furalglucitole Cream,\" Dermatol. Clin. 18: 78-81 (1998) (abstract only).","npl_type":"a","external_id":[],"lens_id":[],"sequence":90,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":20,"text":"Abstract of a publication-M. Maragakis et al., \"Possibilities of Scar Treatment After Thoracic Surgery,\" Drugs Exp. Clin. Res. 21: P:199-206 (1999) (abstract only).","npl_type":"a","external_id":["8846750"],"record_lens_id":"156-793-208-117-567","lens_id":["177-462-485-320-876","156-793-208-117-567"],"sequence":91,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":21,"text":"Abstract of publication-G.H. Willital & H. Heine, \"Efficiency of Contractubex(R) Gel in the Treatment of Fresh Scars After Thoracic Surgery in Children and Adolescents,\" Int. J. Clin. Pharmacol. Res. 14: 193-202 (1994) (abstract only).","npl_type":"a","external_id":["7672876"],"record_lens_id":"049-474-545-239-576","lens_id":["181-570-850-433-24X","049-474-545-239-576"],"sequence":92,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":22,"text":"Publication, H.W. Margraf & T.H. Covey, Jr., \"A Trial of Silver-Zinc-Allantoinate in the Treatment of Leg Ulcers,\" Arch. Surg. 12: 699-704 (1977).","npl_type":"a","external_id":["10.1001/archsurg.1977.01370060031004","871247"],"record_lens_id":"072-772-600-508-943","lens_id":["176-077-222-087-227","072-772-600-508-943","103-023-558-112-519"],"sequence":93,"category":[],"us_category":[],"cited_phase":"APP","rel_claims":[]}},{"npl":{"num":23,"text":"Publication, Remington: The Science and Practice of Pharmacy (19
(a) allantoin;
(b) an emulsifier system including:
(i) beeswax; and
(ii) an anionic emulsifier that is substantially hydrophilic and is soluble in water, the pH of the composition being from about 3.0 to about 6.0 after the addition of an acid,wherein the allantoin is stable in the emulsion across the pH range from about 3.0 to about 6.0."],"number":1,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 1 wherein the pH of the composition is from about 4.5 to about 5.8."],"number":2,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 1 wherein the emulsifier is selected from the group consisting of ammonium lauryl sulfate, sodium lauryl sulfate, sodium laureth sulfate, sodium oleyl succinate, ammonium lauryl sulfosuccinate, sodium dodecylbenzenesulfonate, ammonium laureth sulfate, and sodium lauryl sarcosinate."],"number":3,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 3 wherein the emulsifier is sodium lauryl sulfate."],"number":4,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 1 further comprising administering an additional therapeutic agent in a therapeutically effective quantity."],"number":5,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 5 wherein the additional therapeutic agent is selected from the group consisting of steroids, nonsteroidal anti-inflammatory agents, leukotriene antagonists, and monoclonal antibodies."],"number":6,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 1 wherein the composition further comprises at least one of:
(a) an emollient component comprising at least one ingredient selected from the group consisting of lanolin oil, cetyl alcohol, stearyl alcohol, and cod liver oil;
(b) butylated hydroxytoluene;
(c) at least one herbal extract selected from the group consisting of St. John's wort extract, witch hazel extract, chamomile extract, and arnica extract;
(d) a preservative component comprising at least one preservative selected from the group consisting of methylparaben and propylparaben;
(e) tetrasodium EDTA; and
(f) a solvent component comprising at least one solvent selected from the group consisting of propylene glycol, butylene glycol, and glycerin."],"number":7,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 2 wherein the composition comprises:
an oil-in-water emulsion comprising:
(a) water;
(b) sodium lauryl sulfate;
(c) propylene glycol;
(d) tetrasodium EDTA;
(e) citric acid;
(f) lanolin oil;
(g) cetyl alcohol;
(h) stearyl alcohol;
(i) beeswax;
(j) cod liver oil;
(k) butylated hydroxytoluene;
(l) St. John's wort extract;
(m) witch hazel extract;
(n) chamomile extract;
(o) arnica extract;
(p) methylparaben;
(q) propylparaben;
(r) allantoin; and
(s) fragrance."],"number":8,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 8 wherein the composition comprises:
(a) from about 50% to about 90% of water;
(b) from about 0.5% to about 2.5% of 30% sodium lauryl sulfate;
(c) from about 2.0% to about 9.0% of propylene glycol;
(d) from about 0.05% to about 0.5% of tetrasodium EDTA;
(e) from about 0.05% to about 0.5% of citric acid;
(f) from about 5% to about 15% of lanolin oil;
(g) from about 3% to about 10% of cetyl alcohol;
(h) from about 1% to about 5% of stearyl alcohol;
(i) from about 0.5% to about 2.5% of beeswax;
(j) from about 1.0% to about 7.0% of cod liver oil;
(k) from about 0.1% to about 1.0% of butylated hydroxytoluene;
(l) from about 0.05% to about 0.5% of St. John's wort extract;
(m) from about 0.05% to about 0.5% of witch hazel extract;
(n) from about 0.05% to about 0.5% of chamomile extract;
(o) from about 0.05% to about 0.5% of arnica extract;
(p) from about 0.1% to about 0.5% of methylparaben;
(q) from about 0.1% to about 0.5% of propylparaben;
(r) from about 0.5% to about 2% of allantoin; and
(s) from about 0.05% to about 0.5% of fragrance."],"number":9,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 9 wherein the composition comprises:
(a) from about 55% to about 75% of water;
(b) from about 1.0% to about 2.5% of 30% sodium lauryl sulfate;
(c) from about 3.0% to about 6.0% of propylene glycol;
(d) from about 0.1% to about 0.3% of tetrasodium EDTA;
(e) from about 0.08 to about 0.35% of citric acid;
(f) from about 8.0% to about 12.0% of lanolin oil;
(g) from about 3.5% to about 7.5% of cetyl alcohol;
(h) from about 1.0% to about 3.0% of stearyl alcohol;
(i) from about 1.0% to about 2.5% of beeswax;
(j) from about 1.0% to about 4.0% of cod liver oil;
(k) from about 0.2% to about 0.8% of butylated hydroxytoluene;
(l) from about 0.05% to about 0.15% of St. John's wort extract;
(m) from about 0.05% to about 0.15% of witch hazel extract;
(n) from about 0.05% to about 0.15% of chamomile extract;
(o) from about 0.05% to about 0.15% of arnica extract;
(p) from about 0.15% to about 0.40% of methylparaben;
(q) from about 0.10% to about 0.30% of propylparaben;
(r) from about 0.50% to about 2.0% of allantoin; and
(s) from about 0.1% to about 0.3% of fragrance."],"number":10,"annotation":false,"claim":true,"title":false},{"lines":["The method of claim 10 wherein the composition comprises:
(a) about 68.68% of water;
(b) about 1.9% of sodium lauryl sulfate;
(c) about 5.3% of propylene glycol;
(d) about 0.15% of tetrasodium EDTA;
(e) about 0.12% of citric acid;
(f) about 10.6% of lanolin oil;
(g) about 4.2% of cetyl alcohol;
(h) about 2.0% of stearyl alcohol;
(i) about 1.90% of beeswax;
(j) about 2.0% of cod liver oil;
(k) about 0.5% of butylated hydroxytoluene;
(l) about 0.1% of St. John's wort extract;
(m) about 0.1% of witch hazel extract;
(n) about 0.1% of chamomile extract;
(o) about 0.1% of arnica extract;
(p) about 0.3% of methylparaben;
(q) about 0.25% of propylparaben;
(r) about 1.50% of allantoin; and
(s) about 0.20% of fragrance."],"number":11,"annotation":false,"claim":true,"title":false}]}},"filters":{"npl":[],"notNpl":[],"applicant":[],"notApplicant":[],"inventor":[],"notInventor":[],"owner":[],"notOwner":[],"tags":[],"dates":[],"types":[],"notTypes":[],"j":[],"notJ":[],"fj":[],"notFj":[],"classIpcr":[],"notClassIpcr":[],"classNat":[],"notClassNat":[],"classCpc":[],"notClassCpc":[],"so":[],"notSo":[],"sat":[]},"sequenceFilters":{"s":"SEQIDNO","d":"ASCENDING","p":0,"n":10,"sp":[],"si":[],"len":[],"t":[],"loc":[]}}