NDC11 50804061912

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
50804-0619-12	50804-0619
50804-619-12	50804-619

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MAXIMUM STRENGTH ANTACID AND GASRELIEF	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	GOODSENSE	a9654a96-9bfd-60ea-e053-2995a90ae38d	2023-11-07	Warnings	Exact identifier ndc (package): 50804-619-12 ndc (product): 50804-619 ndc11 (package): 50804061912

Reported adverse events (FAERS/openFDA)#

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