Coricidin HBP Maximum Strength Cold and Flu Day and Night

Product NDC: 11523-0026
Requested package NDC: 11523-0026-1
11-digit product format: 115230026
Labeler code: 11523
Product ID: 11523-0026_eb018f60-134b-9a11-e053-2995a90a11f9
Type: HUMAN OTC DRUG
Nonproprietary name: acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate
Dosage form: KIT
Route: ORAL
Labeler: Bayer HealthCare LLC.
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2020-07-01
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	11523-0026	11523-0026-1	D	Discontinued by firm		2026-07-31

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11523-0026-1	11523002601	1 KIT in 1 BLISTER PACK (11523-0026-1) * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK	1 kit	2020-07-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Coricidin HBP Maximum Strength Cold and Flu Day and Night	Bayer HealthCare LLC.	2023-11-30	HUMAN OTC DRUG LABEL	4