Package 0067-0104-08
Brand: theraflu severe cold relief chest congestion daytime
Generic: acetaminophen, dextromethorphan hbr, guaifenesinPackage Facts
Identity
Package NDC
0067-0104-08
Digits Only
0067010408
Product NDC
0067-0104
Description
245.5 mL in 1 BOTTLE (0067-0104-08)
Marketing
Marketing Status
Brand
theraflu severe cold relief chest congestion daytime
Generic
acetaminophen, dextromethorphan hbr, guaifenesin
Sample Package
No
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "438018c4-8730-1a2d-e063-6294a90a4c46", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1042695"], "spl_set_id": ["8c821671-dc68-4e27-aa87-b4e45ade9817"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245.5 mL in 1 BOTTLE (0067-0104-08)", "package_ndc": "0067-0104-08", "marketing_start_date": "20231201"}], "brand_name": "Theraflu Severe Cold Relief Chest Congestion Daytime", "product_id": "0067-0104_438018c4-8730-1a2d-e063-6294a90a4c46", "dosage_form": "SYRUP", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0067-0104", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu", "brand_name_suffix": "Severe Cold Relief Chest Congestion Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/30mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}