Sinus Relief

Product NDC: 69842-882
11-digit product format: 698420882
Labeler code: 69842
Product ID: 69842-882_523977ae-9c49-4699-8c95-24efba4a09b7
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl
Dosage form: KIT
Labeler: CVS PHARMACY
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-07-01
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Sinus Relief
Brand name suffix: Daytime, Nighttime, Maximum Strength
Listing expiration: 2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1233575	Internal RxNorm lookup
1243679	Internal RxNorm lookup
2634398	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
f6b3ca40-7638-477f-b800-4c28c40ff0a8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69842-882-09	Sinus ReliefDaytime, Nighttime, Maximum Strength	1 in 1 CARTON	KIT	1		14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69842-882	SINUS RELIEF DAYTIME, NIGHTTIME, MAXIMUM STRENGTH (ACETAMINOPHEN, DIPHENHYDRAMINE HCL, GUAIFENESIN, PHENYLEPHRINE HCL) KIT [CVS PHARMACY]	12	Current NDC, Legacy NDC, 1 package rows	20241109_f6b3ca40-7638-477f-b800-4c28c40ff0a8.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 49 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diphenhydramine Hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	Major Pharmaceuticals	04e70311-6412-4a20-84e3-f6e26d5f19ab	2026-02-20	Warnings	Exact identifier application number: M012
Banophen	DIPHENHYDRAMINE HCL	Major Pharmaceuticals	7f2b72cc-d4f7-431f-be61-c103cf8c489e	2026-02-20	Warnings	Exact identifier application number: M012
Diphenhydramine Hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	Major Pharmaceuticals	dca04d80-e781-40b1-e053-2995a90a7010	2026-02-20	Warnings	Exact identifier application number: M012
Diphenhydramine Hydrochloride	DIPHENHYDRAMINE HYDROCHLORIDE	LEADER/ Cardinal Health 110, Inc.	e33cbd1d-1848-145a-e053-2995a90aeb50	2026-02-20	Warnings	Exact identifier application number: M012
Head Congestion and Flu Severe Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Rite Aid Corporation	416080a9-e817-485b-a4ae-6c9d0152c165	2026-02-20	Warnings	Exact identifier application number: M012
Walmart Dye Free Chidrens Allergy Chews	DIPHENHYDRAMINE HCL	WALMART STORES INC	18436026-b0e4-4481-a647-d735a27d0b00	2026-02-19	Warnings	Exact identifier application number: M012
Vaporizing	CAMPHOR	Meijer, Inc.	7afc98d7-f64f-42d5-9022-28ad6b01db8a	2026-02-19	Warnings, Adverse reactions	Exact identifier application number: M012
CHILDRENS COLD AND COUGH	BROMPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE	Kroger Company	8196b482-070e-4d7d-8943-129141f926ee	2026-02-19	Warnings	Exact identifier application number: M012
Walmart Dye Free Chidrens Allergy Chews Bubblegum	DIPHENHYDRAMINE HCL	WALMART STORES INC	9f83d2f0-9718-4f2b-bc7f-e29ba2917412	2026-02-19	Warnings	Exact identifier application number: M012
tussin dm max	DEXTROMETHORPHAN HBR, GUAIFENESIN	Kroger Company	be9aaf66-6c59-4042-88e2-acd920dcf992	2026-02-19	Warnings	Exact identifier application number: M012
Allergy Relief Dye-Free	DIPHENHYDRAMINE HCL	CVS Pharmacy	08459cf4-feb3-4283-88e1-d61e030c57f9	2026-02-19	Warnings	Exact identifier application number: M012
allergy relief	CHLORPHENIRAMINE MALEATE	Rite Aid Corporation	b0d70488-ea1d-4c1d-bd07-53dfb0e4d03c	2026-02-18	Warnings	Exact identifier application number: M012
Walgreens Wild Cherry Pectin Throat Drops	PECTIN	Walgreens	424fda2d-c1e5-0ed9-e063-6394a90a06ea	2026-02-18	Warnings	Exact identifier application number: M012
cough suppressant and topical analgesic	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Target Corporation	df21d9d6-36a9-49cf-a29c-c4a573899bd5	2026-02-18	Warnings, Adverse reactions	Exact identifier application number: M012
Allergy Relief	CHLORPHENIRAMINE MALEATE	Amerisource Bergen	eeda80ff-212d-428e-a0c6-782f271357b4	2026-02-18	Warnings	Exact identifier application number: M012
good sense night time	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	L. Perrigo Company	e47dffdf-5778-4804-8ce2-54c5a72bba3a	2026-02-18	Warnings	Exact identifier application number: M012
Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	United Natural Foods, Inc. dba UNFI	b139e7d6-bf4d-45b9-b7cf-d34e5352095c	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M012
Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Strategic Sourcing Services LLC	bd54bf7a-2304-4c3f-9cd2-bafea217466e	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M012
Creomulsion For Children	DEXTROMETHORPHAN HYDROBROMIDE	Socius Care, LLC	39d0e96c-1cc3-4961-e054-00144ff88e88	2026-02-17	Warnings	Exact identifier application number: M012
Creomulsion Cough Medicine Adult Formula	DEXTROMETHORPHAN HYDROBROMIDE	Socius Care, LLC	39d07486-99b7-5c06-e054-00144ff8d46c	2026-02-17	Warnings	Exact identifier application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2634398	{1 (acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet) / 1 (acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet) } Pack	GPCK	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1233575	acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet	PSN	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1243679	acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet	PSN	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
2634398	daytime 1 (acetaminophen 325 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet) / nighttime 1 (acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet) Pack	PSN	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1233575	acetaminophen 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SCD	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1243679	acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SCD	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1233575	acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet	SY	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1233575	APAP 325 MG / Diphenhydramine Hydrochloride 12.5 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet	SY	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1243679	APAP 325 MG / GG 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SY	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
1243679	APAP 325 MG / Guaifenesin 200 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet	SY	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14
2634398	daytime 1 (acetaminophen 325 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG Oral Tablet) / nighttime 1 (acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG Oral Tablet) Pack	SY	f6b3ca40-7638-477f-b800-4c28c40ff0a8	14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69842-882-09	69842088209	1 KIT in 1 CARTON (69842-882-09) * 10 TABLET, FILM COATED in 1 BLISTER PACK * 10 TABLET, FILM COATED in 1 BLISTER PACK	1 kit	2017-07-01	0000-00-00	No	No	Current