Package 50580-130-24

Brand: tylenol cold plus flu multi-symptom liquid gels day

Generic: acetaminophen, dextromethorphan hydrobromide
NDC Package

Package Facts

Identity

Package NDC 50580-130-24
Digits Only 5058013024
Product NDC 50580-130
Description

2 BLISTER PACK in 1 CARTON (50580-130-24) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b915892-a1b5-c68a-e063-6294a90ab681", "openfda": {"upc": ["0300450691248"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["1867684"], "spl_set_id": ["1c444202-19e9-8d04-e063-6394a90a9294"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50580-130-08)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "50580-130-08", "marketing_start_date": "20250330"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-130-24)  / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "50580-130-24", "marketing_start_date": "20240925"}], "brand_name": "TYLENOL Cold plus Flu Multi-Symptom Liquid Gels Day", "product_id": "50580-130_2b915892-a1b5-c68a-e063-6294a90ab681", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "50580-130", "generic_name": "acetaminophen, Dextromethorphan Hydrobromide", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TYLENOL Cold plus Flu Multi-Symptom Liquid Gels Day", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240925", "listing_expiration_date": "20261231"}