{"adverse_reactions":["ADVERSE REACTIONS: Transient stinging, burning, itching or irritation may occur and normally disappear on discontinuing the medication."],"clinical_pharmacology":["CLINICAL PHARMACOLOGY: Urea gently dissolves the intercellular matrix, which results in loosening the horny layer of skin and shedding scaly skin at regular intervals, thereby softening hyperkeratotic areas."],"contraindications":["CONTRAINDICATIONS: Known hypersensitivity to any of the listed ingredients."],"description":["DESCRIPTION: Each gram of 50% Urea Topical Suspension contains: Urea 50%, Caprylic/Capric Triglyceride, Carbomer, Cetyl Alcohol, Disodium EDTA, Glycerin, Hydroxyethylcellulose, Lactic Acid, Linoleic Acid, PEG-6, Polysorbate 60, Propylene Glycol, Water, Salicylic Acid, Sorbitan Stearate, Titanium Dioxide, Triethanolamine, Tocopheryl Acetate, Xanthan Gum. Urea is a diamide of carbonic acid with the following chemical structure: NH2 | C=O | NH2"],"dosage_and_administration":["DOSAGE AND ADMINISTRATION: Apply 50% UREA TOPICAL SUSPENSION to affected skin twice per day, or as directed by a physician. Rub in until completely absorbed."],"effective_time":"20111111","how_supplied":["HOW SUPPLIED: 50% UREA TOPICAL SUSPENSION is supplied as a 284 g (10 oz) tube, NDC 68032-261-13 Store at controlled room temperature 15°-30° C (59°-86° F). Protect from freezing."],"id":"9e13f6b0-4bf2-4e6c-b94a-6fb54ef43ffd","indications_and_usage":["INDICATIONS AND USES: For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis pilaris, keratosis palmaris, keratoderma, corns and calluses."],"nursing_mothers":["NURSING MOTHERS: It is not known whether or not this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when 50% Urea Topical Suspension is administered to a nursing woman. KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN."],"openfda":{},"package_label_principal_display_panel":["PACKAGING: label"],"pharmacokinetics":["PHARMACOKINETICS: The mechanism of action of topically applied Urea is not yet known."],"precautions":["PRECAUTIONS: This medication is to be used as directed by a physician and should not be used to treat any condition other than that for which it was prescribed. If redness or irritation occurs, discontinue use."],"pregnancy":["PREGNANCY: Pregnancy Category B. Animal reproduction studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, 50% UREA TOPICAL SUSPENSION should be given to a pregnant woman only if clearly needed."],"set_id":"13feb0c4-e139-43ce-8953-8b932d82c79b","spl_product_data_elements":["UREA UREA UREA UREA MEDIUM-CHAIN TRIGLYCERIDES CARBOMER 1342 CETYL ALCOHOL EDETATE DISODIUM GLYCERIN HYPROMELLOSE 2208 (100 MPA.S) LACTIC ACID LINOLEIC ACID POLYETHYLENE GLYCOL 300 POLYSORBATE 60 PROPYLENE GLYCOL WATER SALICYLIC ACID SORBITAN MONOSTEARATE TITANIUM DIOXIDE TROLAMINE XANTHAN GUM"],"version":"4","warnings":["WARNINGS: For external use only. Avoid contact with eyes, lips or mucous membranes."]}