daytime nighttime severe cold and flu

Generic: acetaminophen, dextromethorphan hbr,guaifenesin,/ acetaminophen, dextromethorphan hbr, doxylamine succinate

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

Drug Facts

Product Profile

Brand Name daytime nighttime severe cold and flu
Generic Name acetaminophen, dextromethorphan hbr,guaifenesin,/ acetaminophen, dextromethorphan hbr, doxylamine succinate
Labeler target corp
Dosage Form KIT
Manufacturer
TARGET CORP

Identifiers & Regulatory

Product NDC 11673-844
Product ID 11673-844_0b1e230d-4355-bf61-e063-6394a90a2b2f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-07-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673844
Hyphenated Format 11673-844

Supplemental Identifiers

RxCUI
1426334 2377385

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

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
source: label
Packaging
  • 24 BLISTER PACK in 1 CARTON (11673-844-24) / 1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

11673-844-24 24 BLISTER PACK in 1 CARTON (11673-844-24) / 1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Daytime Nighttime Severe Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "0b1e230d-4355-bf61-e063-6394a90a2b2f", "openfda": {"rxcui": ["1426334", "2377385"], "spl_set_id": ["0b1e230d-4354-bf61-e063-6394a90a2b2f"], "manufacturer_name": ["TARGET CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (11673-844-24)  / 1 KIT in 1 BLISTER PACK *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "11673-844-24", "marketing_start_date": "20240701"}], "brand_name": "Daytime Nighttime Severe Cold and Flu", "product_id": "11673-844_0b1e230d-4355-bf61-e063-6394a90a2b2f", "dosage_form": "KIT", "product_ndc": "11673-844", "generic_name": "acetaminophen, dextromethorphan hbr,guaifenesin,/ acetaminophen, dextromethorphan hbr, doxylamine succinate", "labeler_name": "TARGET CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Nighttime Severe Cold and Flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}