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mapped to comparable property keys"}],"gaps":[{"domain":"identity","state":"unknown","detail":"The barcode is tied to the 28-tablet carton only by upcitemdb's record of a 2021 Target offer; which NDC package code (37000-455-03, or the Wildberry 37000-459 line) this carton carried is not printed in any source read.","observation":"us-drug-facts"},{"domain":"images","state":"unknown","detail":"No licensed photograph of the carton printing 037000082965 is available."},{"domain":"packaging","state":"unknown","detail":"The October 2025 DailyMed 28-tablet carton prints UPC 037000359067 and Target's current 28 ct listing (TCIN 94982167) carries 030772202906; no source says whether either replaced this barcode."},{"domain":"markets","state":"not_researched","detail":"Amazon.com: the 28 Count listing B0014E4JAS, marked (OLD), prints no barcode, and no Amazon listing printing 037000082965 was found."},{"domain":"relationships","state":"unknown","detail":"The label names Sweden as country of manufacture but not the manufacturing company."},{"domain":"images","state":"not_researched","detail":"No product photographs recorded."},{"domain":"schema","state":"schema_gap","detail":"Some specifications retain source labels without comparable property keys."},{"domain":"nutrition","state":"not_researched","detail":"Nutrition declaration or exemption not recorded.","observation":"us-drug-facts"}],"observations":[{"id":"us-drug-facts","label":"US Drug Facts label, Prilosec OTC NDC 37000-455","supportedValues":0,"declaredValues":0,"sourceLinked":0,"stale":false}]},"images":[],"data":{"about":"Prilosec OTC Acid Reducer Tablets 28 ct is a carton of 28 omeprazole 20 mg delayed-release tablets, two 14-day courses, sold over the counter in the United States to treat frequent heartburn.[^upcitemdb][^dailymed] The product is listed with the FDA by The Procter & Gamble Manufacturing Company under NDC 37000-455, with a marketing start of July 2003, and its Drug Facts label names Procter & Gamble of Cincinnati as distributor and Sweden as country of manufacture.[^openfda][^dailymed] Each tablet holds omeprazole equivalent to 20.6 mg omeprazole magnesium and is taken once each morning for 14 days; the maker places the brand in the proton pump inhibitor category.[^dailymed][^maker]\n\nThis barcode was recorded for a Target offer at USD 18.49 on 17 April 2021.[^upcitemdb] The inactive-ingredient list read the same in the December 2021 and October 2025 label versions, while the 28-tablet carton pictured in October 2025 prints UPC 0 37000 35906 7.[^dailymed2021][^dailymed]","aliases":[{"from":null,"name":"Prilosec OTC Acid Reducer Tablets 28ct","type":"search","until":null,"locale":"en"},{"from":null,"name":"037000082965","type":"search","until":null,"locale":null}],"markets":[{"note":"upcitemdb's record for UPC 037000082965 lists a Target offer titled \"Prilosec OTC Acid Reducer Tablets 28ct\" at 18.49 (US dollars, Target.com)","price":"USD 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The carton pictures in those versions print UPC 037000359057 (14 tablets) and 037000359067 (28 tablets), so this is the product's label text, not a reading of the carton with this barcode.","label":"US Drug Facts label, Prilosec OTC NDC 37000-455","market":["US"],"source":"^dailymed","status":"unconfirmed","language":"en","observed":"2025-10-03","valid_from":null,"net_content":null,"pack_format":"carton","piece_count":28,"valid_until":null,"model_number":null,"pack_quantity":null,"ingredients_text":"Active ingredient (in each tablet): Omeprazole delayed-release tablet 20 mg (equivalent to 20.6 mg omeprazole magnesium). Inactive ingredients: glyceryl monostearate, hydroxypropyl cellulose, hypromellose, iron oxide, magnesium stearate, methacrylic acid copolymer, microcrystalline cellulose, paraffin, polyethylene glycol 6000, polysorbate 80, polyvinylpyrrolidone, sodium stearyl fumarate, starch, sucrose, talc, titanium dioxide, triethyl citrate","ingredients_declaration":"listed","ingredients_exempt_basis":null}],"research_gaps":[{"state":"unknown","detail":"The barcode is tied to the 28-tablet carton only by upcitemdb's record of a 2021 Target offer; which NDC package code (37000-455-03, or the Wildberry 37000-459 line) this carton carried is not printed in any source read.","domain":"identity","source":"^upcitemdb","observation":"us-drug-facts"},{"state":"unknown","detail":"No licensed photograph of the carton printing 037000082965 is available.","domain":"images","source":null,"observation":null},{"state":"unknown","detail":"The October 2025 DailyMed 28-tablet carton prints UPC 037000359067 and Target's current 28 ct listing (TCIN 94982167) carries 030772202906; no source says whether either replaced this barcode.","domain":"packaging","source":"^target","observation":null},{"state":"not_researched","detail":"Amazon.com: the 28 Count listing B0014E4JAS, marked (OLD), prints no barcode, and no Amazon listing printing 037000082965 was found.","domain":"markets","source":"^amazon","observation":null},{"state":"unknown","detail":"The label names Sweden as country of manufacture but not the manufacturing company.","domain":"relationships","source":"^dailymed","observation":null}],"specifications":[{"key":null,"mode":null,"note":"openFDA NDC directory, product NDC 37000-455","unit":null,"state":"known","value":"tablet, delayed release","method":"printed","source":"^openfda","property":"Dosage form","qualifier":null,"observation":"us-drug-facts","numeric_value":null},{"key":null,"mode":null,"note":"Omeprazole per tablet, equivalent to 20.6 mg omeprazole magnesium","unit":"mg","state":"known","value":"20","method":"printed","source":"^dailymed","property":"Strength","qualifier":"exact","observation":"us-drug-facts","numeric_value":20},{"key":null,"mode":null,"note":"\"28ct\" in the barcode record; the 28-tablet carton of NDC 37000-455 is two 14-day courses","unit":null,"state":"known","value":"28","method":"printed","source":"^upcitemdb","property":"Tablet count","qualifier":"exact","observation":"us-drug-facts","numeric_value":28},{"key":null,"mode":null,"note":null,"unit":null,"state":"known","value":"oral","method":"printed","source":"^openfda","property":"Route","qualifier":null,"observation":"us-drug-facts","numeric_value":null},{"key":null,"mode":null,"note":"Marketing category NDA; marketing start date 2003-07-14 for product NDC 37000-455","unit":null,"state":"known","value":"NDA021229","method":"printed","source":"^openfda","property":"Application number","qualifier":null,"observation":"us-drug-facts","numeric_value":null},{"key":null,"mode":null,"note":null,"unit":null,"state":"known","value":"store at 20-25°C (68-77°F) and protect from moisture","method":"printed","source":"^dailymed","property":"Storage","qualifier":null,"observation":"us-drug-facts","numeric_value":null}]},"licences":{"database":"ODbL-1.0","text":"CC-BY-SA-4.0","images":"See each image record"}}