Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and Flu

Product NDC: 72854-241
11-digit product format: 728540241
Labeler code: 72854
Product ID: 72854-241_51a46d2a-42d2-29f7-e063-6294a90ae3be
Type: HUMAN OTC DRUG
Nonproprietary name: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and triprolidine hydrochloride
Dosage form: KIT
Labeler: Reckitt Benckiser LLC
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-07-01
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: Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and Flu
Brand name suffix: Maximum Strength
Listing expiration: 2027-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1110988	Internal RxNorm lookup
2549037	Internal RxNorm lookup
2560237	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
dbdafbb4-f3c9-4042-b867-db4d06dc3d61	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
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
30c51294-7ae9-8007-7de6-58222684a0be	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72854-241-10	2023-06-15	Mucinex® Fast-Max ® Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength
72854-241-20	2023-06-15	Mucinex® Fast-Max ® Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength
72854-241-40	2023-06-15	Mucinex® Fast-Max ® Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength
72854-241-10	2023-01-30	Mucinex® Fast-Max ® Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength
72854-241-20	2023-01-30	Mucinex® Fast-Max ® Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength
72854-241-40	2023-01-30	Mucinex® Fast-Max ® Day Cold & Flu and Mucinex Nightshift Night Severe Cold & Flu Maximum Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72854-241-10	Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and FluMaximum Strength	1 in 1 CARTON	KIT	1	4
72854-241-10	Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and FluMaximum Strength	1 in 1 KIT	KIT	1	4
72854-241-20	Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and FluMaximum Strength	1 in 1 KIT	KIT	1	4
72854-241-20	Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and FluMaximum Strength	2 in 1 CARTON	KIT	2	4
72854-241-40	Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and FluMaximum Strength	4 in 1 CARTON	KIT	4	4
72854-241-40	Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and FluMaximum Strength	1 in 1 KIT	KIT	1	4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72854-241-10	EA - Each	72854-241	9aad4a93-c0a1-4bb9-a42e-23d96fa2ad5b	1	2021-06-02
72854-241-20	EA - Each	72854-241	fe70fed1-1535-482f-8c3e-86b65d0b6f5c	1	2021-06-02
72854-241-40	EA - Each	72854-241	189bdcec-3472-4557-a8b5-1c9bd58dad22	1	2021-06-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72854-241	MUCINEX FAST-MAX DAY COLD AND FLU AND MUCINEX NIGHTSHIFT NIGHT SEVERE COLD AND FLU MAXIMUM STRENGTH (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND TRIPROLIDINE HYDROCHLORIDE) KIT [RB HEALTH (US) LLC]	3	Current NDC, Legacy NDC, 6 package rows	20241225_dbdafbb4-f3c9-4042-b867-db4d06dc3d61.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 57 of 178 · 3,551 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Honey Lemon Cough Drops	MENTHOL	CVS Pharmacy	de963dc3-8108-440f-e053-2995a90a906f	2026-01-16	Warnings	Exact identifier application number: M012
CVS SF Menthol Cough Drops	MENTHOL	CVS Pharmacy	e08f8ca3-b683-4964-e053-2a95a90afabb	2026-01-16	Warnings	Exact identifier application number: M012
CVS SF Honey Lemon Cough Drops	MENTHOL	CVS Pharmacy	e0cdeccf-c32f-318a-e053-2a95a90ac401	2026-01-16	Warnings	Exact identifier application number: M012
Mixed Berry Throat and Cough Lozenges	BENZOCAINE	CVS Pharmacy	737b1c88-1a44-68cf-e053-2991aa0a35b6	2026-01-16	Warnings	Exact identifier application number: M012
Walgreens Wild Cherry Throat Drops	PECTIN	Walgreens	4885eca3-c1e9-8350-e063-6394a90ac290	2026-01-16	Warnings	Exact identifier application number: M012
HBP Chest Congestion and Cough Relief	GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE	Walgreens	ff7a1462-9994-4421-85aa-c03488bb04cf	2026-01-16	Warnings	Exact identifier application number: M012
Cough Relief	DEXTROMETHORPHAN HBR	WALGREEN COMPANY	a793acbc-107c-4638-a2d7-65f4e96cafda	2026-01-16	Warnings	Exact identifier application number: M012
MUCUS RELIEF DM	GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE	Walgreens	ca53ec26-d167-1780-e053-2a95a90a5b88	2026-01-16	Warnings	Exact identifier application number: M012
Maximum Strength Congestion and Headache	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Walgreens	88da92d2-92c2-445a-9b70-58996e086014	2026-01-16	Warnings	Exact identifier application number: M012
Maximum Strength Cold and Flu	ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Walgreens	5f638bca-55c2-4ead-8c47-3f15713495da	2026-01-16	Warnings	Exact identifier application number: M012
COLD, Flu and Sore Throat	ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Walgreens	190175bb-c08a-4050-aacf-29a130cbe05c	2026-01-16	Warnings	Exact identifier application number: M012
Night Time Cold and Flu Relief	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	FSA Store Inc. (Caring Mills)	a9bd1efc-51c7-40d0-a4f8-f130ce5b45ff	2026-01-16	Warnings	Exact identifier application number: M012
Allergy Multi-Symptom	ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL	L.N.K. International, Inc.	99147338-f459-4423-ae54-f96fffc1728d	2026-01-15	Warnings	Exact identifier application number: M012
SanaTos Severe Cold Relief Nighttime	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Pharmadel LLC	144aafcc-6ec2-a322-e063-6294a90afc27	2026-01-15	Warnings	Exact identifier application number: M012
SanaTos Severe Cold and Cough Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE	Pharmadel LLC	14484bf5-ff45-b859-e063-6394a90a9a0f	2026-01-15	Warnings	Exact identifier application number: M012
Foster and Thrive Chest Congestion Relief PE PE	GUAIFENESIN/PHENYLEPHRINE	Strategic Sourcing Services LLC	3429aedc-e83d-498a-bfca-03aaf5847b3b	2026-01-15	Warnings	Exact identifier application number: M012
Quality Choice Allergy Relief	DIPHENHYDRAMINE HYDROCHLORIDE	Chain Drug Marketing Association	4b86101c-00f8-4ede-807f-db4273b37b8d	2026-01-15	Warnings	Exact identifier application number: M012
Quality Choice Mucus Relief DM DM	DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN	Chain Drug Marketing Association	d1ba7267-6844-4a14-b518-65277a32e855	2026-01-15	Warnings	Exact identifier application number: M012
ACTINEL DM Pediatric	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	ACTIPHARMA, LLC	f85d8586-423f-48a3-9bb2-bbc5984c7cd3	2026-01-15	Warnings	Exact identifier application number: M012
ACTINEL Diabetic	DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN	ACTIPHARMA, LLC	35c21623-84dd-4151-b35b-e7d30b69c9c0	2026-01-15	Warnings	Exact identifier application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2560237	{1 (acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet) / 1 (acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG / triprolidine hydrochloride 1.25 MG Oral Tablet) } Pack	GPCK	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
2560237	1 daytime (acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet) / 1 nighttime (acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG / triprolidine HCl 1.25 MG Oral Tablet) Pack	PSN	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
1110988	acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet	PSN	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
2549037	acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG / triprolidine HCl 1.25 MG Oral Tablet	PSN	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
1110988	acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SCD	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
2549037	acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG / triprolidine hydrochloride 1.25 MG Oral Tablet	SCD	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
2560237	1 daytime (acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaifenesin 200 MG / phenylephrine HCl 5 MG Oral Tablet) / 1 nighttime (acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG / triprolidine HCl 1.25 MG Oral Tablet) Pack	SY	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
1110988	APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet	SY	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4
2549037	APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG / triprolidine hydrochloride 1.25 MG Oral Tablet	SY	dbdafbb4-f3c9-4042-b867-db4d06dc3d61	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72854-241-10	72854024110	1 KIT in 1 CARTON (72854-241-10) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK	1 kit	2021-07-01	0000-00-00	No	No	Current
72854-241-20	72854024120	2 KIT in 1 CARTON (72854-241-20) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK	2 kit	2021-07-01	0000-00-00	No	No	Current
72854-241-40	72854024140	4 KIT in 1 CARTON (72854-241-40) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK	4 kit	2021-07-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Maximum Strength Mucinex Fast-Max Cold and Flu	Reckitt Benckiser LLC	2026-05-12	HUMAN OTC DRUG LABEL	4