day cold and flu and night severe cold and flu

Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, dextromethorphan hbr, phenylephrine hcl, triprolidine hcl

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name day cold and flu and night severe cold and flu
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, dextromethorphan hbr, phenylephrine hcl, triprolidine hcl
Labeler target corporation
Dosage Form KIT
Routes
ORAL
Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-343
Product ID 11673-343_203f3d03-46d8-3747-e063-6294a90a251e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673343
Hyphenated Format 11673-343

Supplemental Identifiers

RxCUI
1110988 2549037 2560237
UPC
0311673343647

Packaging Origin

Original Packager
true

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 day cold and flu and night severe cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, dextromethorphan hbr, phenylephrine hcl, triprolidine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 1.25 mg
source: label
Packaging
  • 4 BLISTER PACK in 1 CARTON (11673-343-64) / 1 KIT in 1 BLISTER PACK * 6 TABLET, COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

11673-343-64 4 BLISTER PACK in 1 CARTON (11673-343-64) / 1 KIT in 1 BLISTER PACK * 6 TABLET, COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Day Cold and Flu and Night Severe Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "203f3d03-46d8-3747-e063-6294a90a251e", "openfda": {"upc": ["0311673343647"], "rxcui": ["1110988", "2549037", "2560237"], "spl_set_id": ["08ee56d1-b11d-3e36-e063-6294a90acd5f"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (11673-343-64)  / 1 KIT in 1 BLISTER PACK *  6 TABLET, COATED in 1 BLISTER PACK *  4 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "11673-343-64", "marketing_start_date": "20240501"}], "brand_name": "Day Cold and Flu and Night Severe Cold and Flu", "product_id": "11673-343_203f3d03-46d8-3747-e063-6294a90a251e", "dosage_form": "KIT", "product_ndc": "11673-343", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, Triprolidine HCl", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Day Cold and Flu and Night Severe Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}