SINUS PAIN AND CONGESTION

Product NDC: 59779-466
11-digit product format: 597790466
Labeler code: 59779
Product ID: 59779-466_7ecd64a3-bc97-40ba-bc5a-77a47712a780
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen and Phenylephrine HCl
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: CVS Pharmacy
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2005-07-26
Substance: ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Active strength: 325; 5 mg/1; mg/1
Pharmacologic classes: Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
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 PAIN AND CONGESTION
Brand name suffix: DAYTIME
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	325 mg/1
PHENYLEPHRINE HYDROCHLORIDE	5 mg/1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-466-08	SINUS PAIN AND CONGESTIONDAYTIME	2 in 1 CARTON	TABLET, FILM COATED	2		21
59779-466-08	SINUS PAIN AND CONGESTIONDAYTIME	12 in 1 BLISTER PACK	TABLET, FILM COATED	12		21

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
PHENYLEPHRINE HYDROCHLORIDE	ACTIVE INGREDIENT	04JA59TNSJ	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
PHENYLEPHRINE	ACTIVE MOIETY	1WS297W6MV	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
POLYVINYL ALCOHOL	INACTIVE INGREDIENT	532B59J990	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [WOONSOCKET PRESCRIPTION CENTER,INCORPORATED]	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-466	SINUS PAIN AND CONGESTION DAYTIME (ACETAMINOPHEN AND PHENYLEPHRINE HCL) TABLET, FILM COATED [CVS PHARMACY]	20	Current NDC, Legacy NDC, 2 package rows	20241206_c878c7aa-c591-4bae-a1d1-842eaf27c5b1.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 98 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Childrens Giltuss Honey DM Cough	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	a8c5027f-9701-fb07-e053-2a95a90a6029	2025-10-09	Warnings	Exact identifier application number: M012
Childrens Giltuss Honey Cough and Chest Congestion	DEXTROMETHORPHAN HBR, GUAIFENESIN	Gil Pharmaceutical Corp	a8c052d8-fb9f-09f2-e053-2a95a90a37af	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss EX Expectorant	GUAIFENESIN	Gil Pharmaceutical Corp	a8c53c14-ba82-2c68-e053-2a95a90a9894	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss Severe Sinus	OXYMETAZOLINE HCL	Gil Pharmaceutical Corp	ab7fae3b-1f7d-5d0f-e053-2a95a90a148e	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss Honey DM Cough	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	a8c08532-1169-6603-e053-2a95a90a3484	2025-10-09	Warnings	Exact identifier application number: M012
Childrens Giltuss EX Expectorant	GUAIFENESIN	Gil Pharmaceutical Corp	a8c59e6d-c11c-2664-e053-2a95a90a8333	2025-10-09	Warnings	Exact identifier application number: M012
GILTUSS DIABETIC DM	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	bd367ce1-996b-45bc-865e-b6aafe0ea7b0	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss DM	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	1a4fe686-3085-4543-bd6c-f20580b1df50	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss D Allergy and Congestion	CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL	Gil Pharmaceutical Corp	8591003c-c2ec-df65-e053-2a91aa0a42fb	2025-10-09	Warnings	Exact identifier application number: M012
Gilphex	GUAIFENESIN, PHENYLEPHRINE HCL	Gil Pharmaceutical Corp.	e7c8fb97-02cf-4df6-b477-9ff69d6b675d	2025-10-09	Warnings	Exact identifier application number: M012
Childrens Allergy Relief	DIPHENHYDRAMINE HCL	Rite Aid Corporation	d9f26677-ddef-4098-b564-9aa5734e088b	2025-10-09	Warnings	Exact identifier application number: M012
Kalaya Breathe Easy Vaporizing Rub	VAPORIZING RUB	Avaria Health & Beauty Corp	7adf96b1-03af-a87b-e053-2a91aa0a4585	2025-10-08	Warnings	Exact identifier application number: M012
Equate Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Walmart Inc	01e1f418-c232-e89e-e063-6294a90abd35	2025-10-08	Warnings	Exact identifier application number: M012
Equate	OXYMETAZOLINE HCL	Walmart Inc	020942b1-59d4-a19d-e063-6394a90a5d87	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Assorted Flavors 80ct	MENTHOL	Dollar General	425d2e63-f5bc-45fb-b330-967ae64cfddb	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Cherry 200ct	MENTHOL	Dollar General Corporation	a17aece2-abd8-452a-9da8-2e303845900b	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Cherry 30ct	MENTHOL	Dollar General Corporation	b96268da-d6f2-41e4-ba04-ce419376f626	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Cherry 30ct	MENTHOL	Dollar General Corporation	51ccf39a-ae9b-4e6a-856c-002c296f5d07	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Honey Lemon 200ct	MENTHOL	Dollar General Corporation	8f8a9474-f388-4ede-85f2-86222b15ee58	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Honey Lemon 200ct	MENTHOL	Dollar General Corporation	f85f1a15-db7f-4bb5-9313-24702660054e	2025-10-08	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN
04JA59TNSJ	PHENYLEPHRINE HYDROCHLORIDE	61-76-7	PHENYLEPHRINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1046378	acetaminophen 325 MG / phenylephrine HCl 5 MG Oral Tablet	PSN	c878c7aa-c591-4bae-a1d1-842eaf27c5b1	21
1046378	acetaminophen 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SCD	c878c7aa-c591-4bae-a1d1-842eaf27c5b1	21
1046378	APAP 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SY	c878c7aa-c591-4bae-a1d1-842eaf27c5b1	21

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59779-466-08	59779046608	2 BLISTER PACK in 1 CARTON (59779-466-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK	2 blister pack	2005-07-26	0000-00-00	No	No	Current