Daytime Nighttime Cold and Flu

Product NDC: 82501-4672
Requested package NDC: 82501-4672-4
11-digit product format: 825014672
Labeler code: 82501
Product ID: 82501-4672_10d1e5cb-b3f2-4967-a61d-b34764d82f09
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen, Dextromethorphan Hydrobromide,Phenylephrine Hydrochloride DoxylamineSucinate
Dosage form: KIT
Labeler: Gobrands, Inc. (Goodnow)
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2022-04-29
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#

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	82501-4672	82501-4672-4	D	Discontinued by firm		2026-10-15

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

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82501-4672	DAYTIME NIGHTTIME COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE,PHENYLEPHRINE HYDROCHLORIDE DOXYLAMINESUCINATE) KIT [GOBRANDS, INC. (GOODNOW)]	8	Legacy NDC	20241017_2d10bb4a-2c07-406c-8c20-5709f3eb51a2.zip

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
82501-4672-4	82501467204	1 KIT in 1 KIT (82501-4672-4) * 355 mL in 1 BOTTLE * 355 mL in 1 BOTTLE	1 kit	2022-04-29	0000-00-00	No	No	Current