Package 37000-974-60

{"route": ["ORAL"], "spl_id": "4407b4f3-f7a5-d59c-e063-6394a90aba2d", "openfda": {"upc": ["0323900041400"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["a7cf8e2e-7aac-a1fa-e053-2a95a90a561a"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37000-974-60)  / 60 TABLET, COATED in 1 BOTTLE", "package_ndc": "37000-974-60", "marketing_start_date": "20200601"}], "brand_name": "Vicks ZzzQuil Night Pain", "product_id": "37000-974_4407b4f3-f7a5-d59c-e063-6394a90aba2d", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37000-974", "generic_name": "Diphenhydramine Hydrochloride and Acetaminophen", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks ZzzQuil", "brand_name_suffix": "Night Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}