Package 50580-131-24

Brand: tylenol cold plus flu multi-symptom gels night

Generic: acetaminophen, dextromethorphan hydrobromide and doxylamine succinate
NDC Package

Package Facts

Identity

Package NDC 50580-131-24
Digits Only 5058013124
Product NDC 50580-131
Description

2 BLISTER PACK in 1 CARTON (50580-131-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-09-25
Brand tylenol cold plus flu multi-symptom gels night
Generic acetaminophen, dextromethorphan hydrobromide and doxylamine succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "290d3432-b255-7dd1-e063-6394a90af837", "openfda": {"upc": ["0300450692245"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2"], "rxcui": ["1094549"], "spl_set_id": ["1c5386c1-e45d-9dcb-e063-6294a90aff07"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-131-24)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "50580-131-24", "marketing_start_date": "20240925"}], "brand_name": "TYLENOL COLD PLUS FLU MULTI-SYMPTOM GELS NIGHT", "product_id": "50580-131_290d3432-b255-7dd1-e063-6394a90af837", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "50580-131", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide and Doxylamine Succinate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL COLD PLUS FLU MULTI-SYMPTOM GELS NIGHT", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240925", "listing_expiration_date": "20261231"}