nighttime cold and flu liquid
Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
Labeler: target corporationDrug Facts
Product Profile
Brand Name
nighttime cold and flu liquid
Generic Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
Labeler
target corporation
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 650 mg/30mL, dextromethorphan hydrobromide 30 mg/30mL, doxylamine succinate 12.5 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
11673-287
Product ID
11673-287_1ba0e8b6-ef1b-f573-e063-6294a90aca50
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673287
Hyphenated Format
11673-287
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
nighttime cold and flu liquid (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, doxylamine succinate (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/30mL
- 30 mg/30mL
- 12.5 mg/30mL
Packaging
- 354 mL in 1 BOTTLE (11673-287-01)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ba0e8b6-ef1b-f573-e063-6294a90aca50", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2"], "rxcui": ["1043400"], "spl_set_id": ["130ca5f1-2951-ec6f-e063-6394a90a754f"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "354 mL in 1 BOTTLE (11673-287-01)", "package_ndc": "11673-287-01", "marketing_start_date": "20240630"}], "brand_name": "Nighttime Cold and Flu Liquid", "product_id": "11673-287_1ba0e8b6-ef1b-f573-e063-6294a90aca50", "dosage_form": "LIQUID", "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": "11673-287", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nighttime Cold and Flu Liquid", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/30mL"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "12.5 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240630", "listing_expiration_date": "20261231"}