Package 11673-347-02
Brand: day cold and flu
Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hclPackage Facts
Identity
Package NDC
11673-347-02
Digits Only
1167334702
Product NDC
11673-347
Description
2 BLISTER PACK in 1 CARTON (11673-347-02) / 10 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
day cold and flu
Generic
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b941963-8a8d-4148-e063-6294a90a1dfb", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1110988"], "spl_set_id": ["2b941963-8a8c-4148-e063-6294a90a1dfb"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (11673-347-02) / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "11673-347-02", "marketing_start_date": "20250401"}], "brand_name": "DAY COLD AND FLU", "product_id": "11673-347_2b941963-8a8d-4148-e063-6294a90a1dfb", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "11673-347", "generic_name": "acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DAY COLD AND FLU", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}