{"active_ingredient":["OTC - ACTIVE INGREDIENT Loratadine, USP 10 mg Pseudoephedrine sulfate, USP 240 mg"],"dosage_and_administration":["DOSAGE & ADMINISTRATION do not divide, crush, chew or dissolve the tablet adults and children 12 years and over 1 tablet daily with a full glass of water; not more than 1 tablet in 24 hours children under 12 years of age ask a doctor consumers with liver or kidney disease ask a doctor"],"dosage_and_administration_table":["<table ID=\"inv-8cfe9702-4e1c-4f55-8fcd-dad01b6bd19c\" border=\"1\"> <col span=\"1\" width=\"273px\"/> <col span=\"1\" width=\"350px\"/> <tbody> <tr> <td>adults and children 12 years and over</td> <td>1 tablet daily with a full glass of water; not more than 1 tablet in 24 hours</td> </tr> <tr> <td>children under 12 years of age</td> <td>ask a doctor</td> </tr> <tr> <td>consumers with liver or kidney disease</td> <td>ask a doctor</td> </tr> </tbody> </table>"],"effective_time":"20170310","id":"4a679629-b79a-3e73-e054-00144ff88e88","inactive_ingredient":["INACTIVE INGREDIENT calcium carbonate, colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, iron oxide black, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, sodium alginate, sodium citrate, talc and titanium dioxide"],"indications_and_usage":["INDICATIONS & USAGE temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing itchy, watery eyes runny nose itching of the nose or throat reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies temporarily restores freer breathing through the nose"],"openfda":{},"package_label_principal_display_panel":["PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION DRUG: Loratadine and Pseudoephedrine Sulfate GENERIC: Loratadine and Pseudoephedrine Sulfate DOSAGE: TABLET, FILM COATED, EXTENDED RELEASE ADMINSTRATION: ORAL NDC: 61786-143-57 ACTIVE INGREDIENT(S): LORATADINE 10mg in 1 PSEUDOEPHEDRINE SULFATE 240mg in 1 INACTIVE INGREDIENT(S): CALCIUM CARBONATE PROPYLENE GLYCOL SHELLAC STARCH, PREGELATINIZED CORN POVIDONE TALC SODIUM ALGINATE SODIUM CITRATE POLYETHYLENE GLYCOLS CELLULOSE, MICROCRYSTALLINE HYDROXYPROPYL CELLULOSE COLLOIDAL SILICON DIOXIDE HYPROMELLOSES FERROSOFERRIC OXIDE MAGNESIUM STEARATE LACTOSE MONOHYDRATE TITANIUM DIOXIDE COLOR: white SHAPE: CAPSULE SCORE: No score SIZE: 17 mm IMPRINT: RX724 PACKAGING: 5 in 1 BOTTLE MM1 MM2"],"purpose":["OTC - PURPOSE Antihistamine Nasal decongestant"],"questions":["OTC - QUESTIONS call 1-800-406-7984 Keep the carton. It contains important information. See end panel for expiration date. Distributed By MAJOR PHARMACEUTICALS 31778 Enterprise Drive, LIVONIA, MI 48150, USA"],"set_id":"06ba2cf5-7cb1-44cf-8cda-3974bf964ca7","spl_product_data_elements":["Loratadine and Pseudoephedrine Sulfate Loratadine and Pseudoephedrine Sulfate CALCIUM CARBONATE PROPYLENE GLYCOL SHELLAC STARCH, PREGELATINIZED CORN POVIDONE TALC SODIUM ALGINATE SODIUM CITRATE POLYETHYLENE GLYCOLS CELLULOSE, MICROCRYSTALLINE HYDROXYPROPYL CELLULOSE (TYPE H) SILICON DIOXIDE HYPROMELLOSES FERROSOFERRIC OXIDE MAGNESIUM STEARATE LACTOSE MONOHYDRATE TITANIUM DIOXIDE LORATADINE LORATADINE PSEUDOEPHEDRINE SULFATE PSEUDOEPHEDRINE TABLET, FILM COATED, EXTENDED RELEASE RX724"],"spl_unclassified_section":["SPL UNCLASSIFIED sodium: contains 10 mg/tablet calcium: contains 25 mg/tablet TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE. (for bottle cartons/labels only) TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING. (for blister cartons only) store between 20° C to 25° C (68° F to 77° F). protect from light and store in a dry place"],"version":"2","warnings":["WARNINGS if you have ever had an allergic reaction to this product or any of its ingredients if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. heart disease thyroid disease high blood pressure diabetes trouble urinating due to an enlarged prostate gland liver or kidney disease. Your doctor should determine if you need a different dose. Taking more than directed may cause drowsiness. an allergic reaction to this product occurs. Seek medical help right away. symptoms do not improve within 7 days or are accompanied by a fever nervousness, dizziness or sleeplessness occurs ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)."]}