NDC 63824-041-71

This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.

Requested NDC: 63824-041-71
Product root: 63824-041
Identity scope: Package
Primary current NDC product row: Not present

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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	63824-041	63824-041-71	D	Discontinued by firm		2026-07-31

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mucinex D Maximum Strength	GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE	Reckitt Benckiser LLC	d9264518-2f2c-498f-b733-6f3397336a01	2026-04-21	Warnings	Exact identifier ndc (package): 63824-041-71 ndc (product): 63824-041 ndc11 (package): 63824004171