NDC11 00121176230

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
00121-1762-30	00121-1762
0121-1762-30	0121-1762

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
Mag-AL Plus XS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND DIMETHICONE	PAI Holdings, LLC dba PAI Pharma	db0c47ab-5296-4195-9fa6-2e338b665094	2024-11-12	Warnings	Exact identifier ndc (package): 0121-1762-30 ndc (product): 0121-1762 ndc11 (package): 00121176230

Reported adverse events (FAERS/openFDA)#

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