Package 0067-7917-06

{"route": ["ORAL"], "spl_id": "1006345e-67d7-8b81-e063-6294a90ad7cd", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1659967"], "spl_set_id": ["c0689223-5c90-4dbc-bbfa-f94e267504c3"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-7917-06)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-7917-06", "marketing_start_date": "20120924"}], "brand_name": "Theraflu Daytime Severe Cold and Cough", "product_id": "0067-7917_1006345e-67d7-8b81-e063-6294a90ad7cd", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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": "0067-7917", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu", "brand_name_suffix": "Daytime Severe Cold and Cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120924", "listing_expiration_date": "20261231"}