Package 0031-8752-18

{"route": ["ORAL"], "spl_id": "156ef02d-2284-6dc7-e063-6294a90a3be9", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1375932"], "spl_set_id": ["89360fa8-014d-4da8-bb1c-197e3aa52256"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8752-12)  / 118 mL in 1 BOTTLE", "package_ndc": "0031-8752-12", "marketing_start_date": "20150701"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8752-18)  / 237 mL in 1 BOTTLE", "package_ndc": "0031-8752-18", "marketing_start_date": "20150701"}], "brand_name": "Robitussin Severe Multi-Symptom Cough Cold Flu Nighttime", "product_id": "0031-8752_156ef02d-2284-6dc7-e063-6294a90a3be9", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0031-8752", "generic_name": "acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin Severe Multi-Symptom Cough Cold Flu Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}], "application_number": "M0012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150701", "listing_expiration_date": "20261231"}