SINUS RELIEF

Product NDC: 59779-881
11-digit product format: 597790881
Labeler code: 59779
Product ID: 59779-881_c20108b1-2861-45da-b032-8b6c7d5b6424
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen, Guaifenesin, Diphenhydramine HCl, Phenylephrine HCl
Dosage form: KIT
Labeler: CVS Pharmacy
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2013-06-30
Marketing end: 2019-11-17
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	59779-881		D	Discontinued by firm		2026-10-16
excluded package	package	59779-881	59779-881-09	D	Discontinued by firm		2026-10-16

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 · 24 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59779-881-09	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59779-881-09	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59779-881-09	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59779-881-09	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59779-881-09	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59779-881-09	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59779-881-09	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59779-881-09	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59779-881-09	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59779-881-09	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	59779-881-09	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	59779-881-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59779-881-09	EA - Each	59779-881	a439d2ea-ab9e-48d5-82f8-aa37f7bc3679	1	2016-09-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
DIPHENHYDRAMINE HYDROCHLORIDE	ACTIVE INGREDIENT	TC2D6JAD40	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
GUAIFENESIN	ACTIVE INGREDIENT	495W7451VQ	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
PHENYLEPHRINE HYDROCHLORIDE	ACTIVE INGREDIENT	04JA59TNSJ	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
DIPHENHYDRAMINE	ACTIVE MOIETY	8GTS82S83M	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
GUAIFENESIN	ACTIVE MOIETY	495W7451VQ	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
PHENYLEPHRINE	ACTIVE MOIETY	1WS297W6MV	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
MALTODEXTRIN	INACTIVE INGREDIENT	7CVR7L4A2D	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	SINUS RELIEF MAXIMUM STRENGTH DAYTIME AND NIGHTTIME SINUS PAIN (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	2