Daytime Nighttime Severe Cold and Flu

Product NDC: 55319-813
Requested package NDC: 55319-813-16
11-digit product format: 553190813
Labeler code: 55319
Product ID: 55319-813_a6f5dab6-342d-496b-b2ae-e48d6e29d487
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen Dextromethorphan HBr Guaifenesin Phenylephrine HCL DoxylamineSucinate
Dosage form: KIT
Labeler: Family Dollar (FAMILY WELLNESS)
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-07-31
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2020-12-31
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	55319-813	55319-813-16	D	Discontinued by firm		2026-10-20

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 · 5 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2022-08-30 03:57 UTC · source 2022-08-29	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55319-813-16	2023-01-20	C162847	48780-1	d6a99b39-84c8-a426-e053-dadaa90af4c2	Drug Facts
55319-813-16	2022-01-28	C162847	48780-1	d6a99b39-84c8-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55319-813	DAYTIME NIGHTTIME SEVERE COLD AND FLU (ACETAMINOPHEN DEXTROMETHORPHAN HBR GUAIFENESIN PHENYLEPHRINE HCL DOXYLAMINESUCINATE) KIT [FAMILY DOLLAR (FAMILY WELLNESS)]	2	Legacy NDC	20230122_f80b321f-fcef-4a07-a82c-28c0f99d13f8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55319-813-16	55319081316	1 KIT in 1 KIT (55319-813-16) * 237 mL in 1 BOTTLE * 237 mL in 1 BOTTLE	1 kit	2019-07-31	0000-00-00	No	No	Current