Package 41163-849-24
Brand: nighttime cold and flu relief multi symptom
Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinatePackage Facts
Identity
Package NDC
41163-849-24
Digits Only
4116384924
Product NDC
41163-849
Description
24 BLISTER PACK in 1 CARTON (41163-849-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
nighttime cold and flu relief multi symptom
Generic
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cd2634c-03ae-46cc-84a0-06a19d2e4ef1", "openfda": {"upc": ["0041163492400"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2"], "rxcui": ["1094549"], "spl_set_id": ["1aba9b7c-8328-4a9f-8ce2-39648b2d8ae4"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (41163-849-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "41163-849-24", "marketing_start_date": "20190930"}], "brand_name": "Nighttime Cold and Flu Relief Multi Symptom", "product_id": "41163-849_2cd2634c-03ae-46cc-84a0-06a19d2e4ef1", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "41163-849", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nighttime Cold and Flu Relief", "brand_name_suffix": "Multi Symptom", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190930", "listing_expiration_date": "20261231"}