NDC11 10572001201

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
10572-0012-01	10572-0012
10572-0012-1	10572-0012
10572-012-01	10572-012

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
SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE	SODIUM SULFATE, POTASSIUM SULFATE, MAGNESIUM SULFATE	Affordable Pharmaceuticals, LLC	f86bdcc8-e643-4160-89ae-01c89bee842d	2025-11-30	Warnings, Adverse reactions	Exact identifier ndc (package): 10572-012-01 ndc (product): 10572-012 ndc11 (package): 10572001201

Reported adverse events (FAERS/openFDA)#

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