Mucus Relief Daytime Severe Cold Nighttime Cold and Flu

Product NDC: 11673-906
11-digit product format: 116730906
Labeler code: 11673
Product ID: 11673-906_6879cd08-f755-4264-8777-8f35265d30b3
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCL,Guaifenesin
Dosage form: KIT
Labeler: TARGET Corporation
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-09-30
Marketing end: 2025-08-29
Active strength: 0
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	11673-906		D	Discontinued by firm		2026-10-12
excluded package	package	11673-906	11673-906-24	D	Discontinued by firm		2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product	11673-906		D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	11673-906	11673-906-24	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-906	MUCUS RELIEF DAYTIME SEVERE COLD NIGHTTIME COLD AND FLU MAXIMUM STRENGTH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL,GUAIFENESIN) KIT [TARGET CORPORATION]	2	Legacy NDC	20221118_71e75e55-6e5f-413f-9abd-1a7393bb88b2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-906-24	11673090624	1 KIT in 1 KIT (11673-906-24) * 16 BLISTER PACK in 1 CARTON > 1 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON > 1 CAPSULE in 1 BLISTER PACK	1 kit	2019-09-30	2025-08-29	No	No	Current