Package 0067-0104-08

Brand: theraflu severe cold relief chest congestion daytime

Generic: acetaminophen, dextromethorphan hbr, guaifenesin
NDC Package

Package 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
Marketed Since 2023-12-01
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"}