daytime severe and nighttime severe cold and flu

Generic: daytime severe - acetaminophen, dextromethorphan hbr, guaifenesin and nighttime severe-acetaminophen, dextromethorphan hbr, doxylamine succinate

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

Drug Facts

Product Profile

Brand Name daytime severe and nighttime severe cold and flu
Generic Name daytime severe - acetaminophen, dextromethorphan hbr, guaifenesin and nighttime severe-acetaminophen, dextromethorphan hbr, doxylamine succinate
Labeler target corporation
Dosage Form KIT
Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-739
Product ID 11673-739_09286efa-2aca-fb1c-e063-6394a90a3afa
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 11673739
Hyphenated Format 11673-739

Supplemental Identifiers

RxCUI
1042675 1042695 1369842 1431245 2637731

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 daytime severe and nighttime severe cold and flu (source: ndc)
Generic Name daytime severe - acetaminophen, dextromethorphan hbr, guaifenesin and nighttime severe-acetaminophen, dextromethorphan hbr, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 30 ml
  • 650 mg
  • 20 mg
  • 12.5 mg
  • 10 mg
  • 15 ml
  • 325 mg
  • 200 mg
  • 5 mg
source: label
Packaging
  • 1 KIT in 1 BOTTLE (11673-739-02) * 355 mL in 1 BOTTLE * 355 mL in 1 BOTTLE
source: ndc

Packages (1)

11673-739-02 1 KIT in 1 BOTTLE (11673-739-02) * 355 mL in 1 BOTTLE * 355 mL in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Daytime Severe and Nighttime Severe cold and flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "09286efa-2aca-fb1c-e063-6394a90a3afa", "openfda": {"rxcui": ["1042675", "1042695", "1369842", "1431245", "2637731"], "spl_set_id": ["09286d15-b63f-a9de-e063-6294a90ab948"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BOTTLE (11673-739-02)  *  355 mL in 1 BOTTLE *  355 mL in 1 BOTTLE", "package_ndc": "11673-739-02", "marketing_start_date": "20240501"}], "brand_name": "Daytime Severe and Nighttime Severe cold and flu", "product_id": "11673-739_09286efa-2aca-fb1c-e063-6394a90a3afa", "dosage_form": "KIT", "product_ndc": "11673-739", "generic_name": "Daytime Severe - Acetaminophen, Dextromethorphan HBr, Guaifenesin and Nighttime Severe-Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Severe and Nighttime Severe cold and flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}