daytime severe cold and cough and nighttime severe cold and cough

Generic: acetaminophen, dextromethorphan hbr, diphenhydramine hcl, phenylephrine hcl

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

Drug Facts

Product Profile

Brand Name daytime severe cold and cough and nighttime severe cold and cough
Generic Name acetaminophen, dextromethorphan hbr, diphenhydramine hcl, phenylephrine hcl
Labeler target corporation
Dosage Form KIT
Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-542
Product ID 11673-542_62eec235-431f-4429-b173-d4a9b45a4e36
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part341
Listing Expiration 2026-12-31
Marketing Start 2017-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673542
Hyphenated Format 11673-542

Supplemental Identifiers

RxCUI
1428880 1659960 1659967

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 cold and cough and nighttime severe cold and cough (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, diphenhydramine hcl, phenylephrine hcl (source: ndc)
Application Number part341 (source: ndc)

Resolved Composition

Strengths
  • 650 mg
  • 20 mg
  • 10 mg
  • 25 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (11673-542-12) * 6 POWDER, FOR SOLUTION in 1 CARTON (11673-540-06) * 6 POWDER, FOR SOLUTION in 1 CARTON (11673-541-06)
source: ndc

Packages (1)

11673-542-12 1 KIT in 1 CARTON (11673-542-12) * 6 POWDER, FOR SOLUTION in 1 CARTON (11673-540-06) * 6 POWDER, FOR SOLUTION in 1 CARTON (11673-541-06)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

daytime severe cold and cough and nighttime severe cold and cough ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "62eec235-431f-4429-b173-d4a9b45a4e36", "openfda": {"rxcui": ["1428880", "1659960", "1659967"], "spl_set_id": ["62eec235-431f-4429-b173-d4a9b45a4e36"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11673-542-12)  *  6 POWDER, FOR SOLUTION in 1 CARTON (11673-540-06)  *  6 POWDER, FOR SOLUTION in 1 CARTON (11673-541-06)", "package_ndc": "11673-542-12", "marketing_start_date": "20170731"}], "brand_name": "daytime severe cold and cough and nighttime severe cold and cough", "product_id": "11673-542_62eec235-431f-4429-b173-d4a9b45a4e36", "dosage_form": "KIT", "product_ndc": "11673-542", "generic_name": "Acetaminophen, Dextromethorphan HBr, Diphenhydramine HCl, Phenylephrine HCl", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "daytime severe cold and cough and nighttime severe cold and cough", "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20170731", "listing_expiration_date": "20261231"}