{"adverse_reactions":["These highlights do not include all the information needed to use. See full prescribing information for Lactulose Initial U.S. Approval. To report suspected adverse reactions contact lannet Company Inc at 1-800-332-1088 Label Adverse Reactions"],"clinical_pharmacology":["label Clinical Pharmacology"],"contraindications":["These Highlights do not include all the information needed to use. See full prescribing information for Lactulose Intial U.S. Approval Label Contraindications"],"description":["Label Description"],"dosage_and_administration":["These highlights do not include all the information needed to use. See full prescribing information for Lactulose Initial U.S. Approval Label-Dosage and Administration"],"effective_time":"20230110","how_supplied":["label How Supplied"],"id":"f1f0ab04-0096-9db4-e053-2995a90aa04c","indications_and_usage":["These highlights do not include all the information needed to use. See full prescribing information for Lactulose Initial U.S. approval label indications and usage"],"openfda":{},"overdosage":["label-overdose Label Overdose cont"],"package_label_principal_display_panel":["Display image"],"precautions":["label precautions"],"set_id":"b8434772-26c8-fce9-e053-2995a90abc7c","spl_product_data_elements":["Lactulose Solution Lactulose Solution FD&C YELLOW NO. 6 FD&C BLUE NO. 1 WATER LACTULOSE LACTULOSE SODIUM HYDROXIDE"],"version":"2","warnings":["label warnings"]}