Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu

Product NDC: 69842-462
11-digit product format: 698420462
Labeler code: 69842
Product ID: 69842-462_b417d1de-3020-4a0b-8589-a4612acd9957
Type: HUMAN OTC DRUG
Nonproprietary name: Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, Acetaminophen, Diphenhydramine HCl, Phenylephrine HCl
Dosage form: KIT
Labeler: CVS Pharmacy
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-04-30
Marketing end: 2027-01-30
NDC exclude flag: No
Current FDA listing: Yes

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 · 26 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
2025-04-01 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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`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	69842-462-12	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69842-462-12	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69842-462-12	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69842-462-12	`1332a3947898…`	`d4bfe170f9cd…`

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: Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu
Brand name suffix: Maximum Strength

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1043543	Internal RxNorm lookup
1375932	Internal RxNorm lookup
2637728	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
91c803c8-6cf8-4ff6-b376-ea6d65f9f227	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e4e263da-1c53-440f-bb80-b7a575843b5a	Product name	1	20260313
d2168cac-a261-415a-9c78-3522859fa720	Product name	3	20251124
bf324df6-7127-7deb-def5-2681c136cd03	Product name	3	20250325
05a8cdd1-eeb8-409e-b938-0778225eca7d	Product name	4	20250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9	Product name	8	20250220
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
f489e8f3-5c9e-4818-b539-a73587edcfc7	Product name	2	20240229
0f7ae452-206d-4fc4-868d-56fc47074084	Product name	1	20231011
43a1ed49-eae2-4840-8075-cb4b33478540	Product name	1	20230425
ba088a92-ab5e-b2d4-e908-f5ea691b7587	Product name	7	20210201
b5abe2e3-39a1-43eb-9bff-f3c1653fe3df	Product name	2	20190930
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814	Product name	3	20150910
4fe95224-f543-4dbb-9445-8cca122b48c8	Product name	1	20150609
e8718272-64cb-4436-969b-176c3067c8f4	Product name	1	20150609
106ff02a-57e1-4c4c-a307-fd582ff4e311	Product name	1	20150212
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
42f3c020-f1b3-89bc-7bdc-e1f10e680485	Product name	1	20140508
76633df9-0d59-4b88-03ed-21dee1b966f8	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508
e949165d-714d-e548-2b76-0cb5def16f30	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69842-462-12	2025-07-01	C162847	48780-1	f386c64a-3a8d-0266-e053-dadaa90a7c1a	Drug Facts
69842-462-12	2023-01-30	C162847	48780-1	f386c64a-3a8d-0266-e053-dadaa90a7c1a	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69842-462-12	Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and FluMaximum Strength	1 in 1 KIT	KIT	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69842-462	DAYTIME MUCUS RELIEF SEVERE CONGESTION AND COUGH AND NIGHTTIME COLD AND FLU MAXIMUM STRENGTH (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL) KIT [CVS PHARMACY]	2	Current NDC, Legacy NDC, 1 package rows	20191101_91c803c8-6cf8-4ff6-b376-ea6d65f9f227.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 71 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Honey Lemon cough drops	MENTHOL	Walmart Stores Inc.	317bbd33-6087-3af1-e054-00144ff8d46c	2025-12-21	Warnings	Exact identifier application number: M012
Good Sense Nasal Decongestant	PSEUDOEPHEDRINE HCL	L. Perrigo Company	455b35b4-3969-411b-8036-887615d71e11	2025-12-21	Warnings	Exact identifier application number: M012
Menthol Cough Drop	MENTHOL	Safeway Inc.	4a4f7f82-1b6c-7082-e054-00144ff88e88	2025-12-20	Warnings	Exact identifier application number: M012
Cherry Cough Drop	MENTHOL	Safeway Inc.	4a52c0c2-8659-2819-e054-00144ff8d46c	2025-12-20	Warnings	Exact identifier application number: M012
Signature Care Cherry Cough Drops	MENTHOL	Safeway	a733e905-af15-d3ea-e053-2a95a90aa7c3	2025-12-20	Warnings	Exact identifier application number: M012
Signature Care Honey Lemon Cough Drops	MENTHOL	Safeway	a742449f-c76b-2b91-e053-2a95a90ae4d2	2025-12-20	Warnings	Exact identifier application number: M012
Cherry Sore Throat Lozenge	BENZOCAINE	TopCo	60b876e7-c642-5ce8-e053-2a91aa0abd6e	2025-12-20	Warnings	Exact identifier application number: M012
menthol cough drops	MENTHOL	Topco Associates	366cc6b1-beff-29d2-e054-00144ff88e88	2025-12-20	Warnings	Exact identifier application number: M012
cherry cough drops	MENTHOL	TopCo Associates	3fef2117-7311-1e66-e054-00144ff8d46c	2025-12-20	Warnings	Exact identifier application number: M012
honey lemon cough drops	MENTHOL	Topco Associates	3ff1bf05-e407-3b67-e054-00144ff8d46c	2025-12-20	Warnings	Exact identifier application number: M012
sugar free menthol cough drops	MENTHOL	Topco Associates	36727f0c-d6d2-28a3-e054-00144ff8d46c	2025-12-20	Warnings	Exact identifier application number: M012
sugar free honey lemon cough drops	MENTHOL	Topco Associates	36824bee-607e-7095-e054-00144ff8d46c	2025-12-20	Warnings	Exact identifier application number: M012
Mixed Berry Sore Throat Lozenges	BENZOCAINE	Topco Associates	7a00c771-9231-e877-e053-2a91aa0ac96e	2025-12-20	Warnings	Exact identifier application number: M012
MUCUS RELIEF	GUAIFENESIN 400 MG	NUVICARE LLC	e25b440e-f389-443f-b333-c66ad1747158	2025-12-19	Warnings	Exact identifier application number: M012
Cold and Flu severe	ACETAMINOPHEN,DEXTROMETHORPHAN HBR,GUAIFENESIN,PHENYLEPHRINE HCL	Wal-Mart Stores Inc	9fca25dc-f63e-487a-8b7c-84d65ea51cb5	2025-12-19	Warnings	Exact identifier application number: M012
Cold and Flu Severe	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	Geiss, Destin & Dunn Inc.	a7d2eaee-484e-43aa-8ae3-0e050219383f	2025-12-19	Warnings	Exact identifier application number: M012
Cherry Cough Drops	MENTHOL	Publix	66d8e5f7-9766-57f3-e053-2991aa0a7e17	2025-12-19	Warnings	Exact identifier application number: M012
Honey Lemon Cough Drops	MENTHOL	Publix	66e89fa3-ee09-1d16-e053-2a91aa0ae17c	2025-12-19	Warnings	Exact identifier application number: M012
Poly-Vent DM	DEXTROMETHORPHAN HBR, GUAIFENESIN AND PSEUDOEPHEDRINE HCL	Poly Pharmaceuticals, Inc.	739329ae-0b62-4eab-a07d-867b5d3d61e0	2025-12-19	Warnings	Exact identifier application number: M012
Chest Congestion and Cough Relief DM	DEXTROMETHORPHAN HBR, GUAIFENESIN	ARMY AND AIR FORCE EXCHANGE SERVICE	89494a7c-cdbf-48f1-aaa9-2e57d4388a68	2025-12-19	Warnings	Exact identifier application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2637728	{1 (acetaminophen 32.5 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution) / 1 (dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution) } Pack	GPCK	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
2637728	1 daytime (dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution) / 1 nighttime (acetaminophen 325 MG / diphenhydrAMINE HCl 12.5 MG / phenylephrine HCl 5 MG in 10 mL Oral Solution) Pack	PSN	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	acetaminophen 650 MG / diphenhydrAMINE HCl 25 MG / phenylephrine HCl 10 MG in 20 mL Oral Solution	PSN	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1043543	dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution	PSN	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	acetaminophen 32.5 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution	SCD	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1043543	dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution	SCD	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
2637728	1 daytime (dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution) / 1 nighttime (acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution) Pack	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	acetaminophen 325 MG / diphenhydramine HCl 12.5 MG / phenylephrine HCl 5 MG per 10 ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	acetaminophen 650 MG / diphenhydramine HCl 25 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	APAP 32.5 MG/ML / Diphenhydramine Hydrochloride 1.25 MG/ML / Phenylephrine Hydrochloride 0.5 MG/ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	APAP 325 MG / diphenhydramine hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG per 10 ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1375932	APAP 650 MG / diphenhydramine hydrochloride 25 MG / phenylephrine hydrochloride 10 MG per 20 ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1043543	dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3
1043543	dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution	SY	91c803c8-6cf8-4ff6-b376-ea6d65f9f227	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69842-462-12	69842046212	1 KIT in 1 KIT (69842-462-12) * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC	1 kit	2018-04-30	2027-01-30	No	No	Current