Package 11673-113-07

{"route": ["ORAL"], "spl_id": "39fadcca-6c94-39b8-e063-6394a90a89a2", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659960"], "spl_set_id": ["df488727-b913-440b-9a0b-cce3ae143bf2"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER, FOR SOLUTION in 1 CARTON (11673-113-07)", "package_ndc": "11673-113-07", "marketing_start_date": "20130628"}], "brand_name": "up and up nighttime flu and severe cold and cough", "product_id": "11673-113_39fadcca-6c94-39b8-e063-6394a90a89a2", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "11673-113", "generic_name": "Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up", "brand_name_suffix": "nighttime flu and severe cold and cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130628", "listing_expiration_date": "20261231"}