Package 0067-0100-06

{"route": ["ORAL"], "spl_id": "41da2cea-21f3-4162-b20d-ddbc66270b35", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2670598"], "spl_set_id": ["2b962d87-6ff5-4c0f-8504-e5b61c940612"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-0100-06)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-0100-06", "marketing_start_date": "20231201"}, {"sample": false, "description": "1000 PACKET in 1 CONTAINER (0067-0100-99)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-0100-99", "marketing_start_date": "20250101"}], "brand_name": "Theraflu Severe Cold Relief Daytime", "product_id": "0067-0100_41da2cea-21f3-4162-b20d-ddbc66270b35", "dosage_form": "POWDER, FOR SOLUTION", "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": "0067-0100", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HBr", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold Relief Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}