Mucinex Fast Max

Product NDC: 63824-792
Requested package NDC: 63824-792-01
11-digit product format: 638240792
Labeler code: 63824
Product ID: 63824-792_f435e7a9-e7d7-4b5c-ab62-909519111679
Type: HUMAN OTC DRUG
Nonproprietary name: Guaifenesin, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, Acetaminophen, and Diphenhydrmaine Hydrochloride
Dosage form: KIT
Labeler: RB Health (US) LLC
Application: part341
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2018-12-15
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2023-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	63824-792	63824-792-01	D	Discontinued by firm		2026-10-05

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 · 6 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63824-792-01	2022-01-30	C162847	48780-1	d6a99b39-3555-a426-e053-dadaa90af4c2	Mucinex® Fast Max ® Day Time Severe Congestion & Cough and Night Time Cold & Flu
63824-792-01	2022-01-28	C162847	48780-1	d6a99b39-3555-a426-e053-dadaa90af4c2	Mucinex® Fast Max ® Day Time Severe Congestion & Cough and Night Time Cold & Flu

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63824-792-01	EA - Each	63824-792	56b01713-55d6-43cb-97e1-1566befc6498	1	2020-09-14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63824-792-01	63824079201	1 KIT in 1 PACKAGE, COMBINATION (63824-792-01) * 2 BLISTER PACK in 1 CARTON (63824-515-01) > 10 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK	1 kit	2018-12-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Mucinex Fast-Max Severe Congestion and Cough	RB Health (US) LLC	2023-09-27	HUMAN OTC DRUG LABEL	3