SODIUM IODIDE I 123

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: SODIUM IODIDE I 123
Generic name: SODIUM IODIDE I 123
Manufacturer: Curium US LLC
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 493fa2ab-4eb0-4434-9739-3079b2f0e272
SPL ID: 24b19127-9a67-0ddf-e063-6394a90ae0b5
Version: 10
Effective date: 2024-10-17
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:46:10

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	071909	derived:openfda.application_number
application applno	ANDA	071910	derived:openfda.application_number
application number		ANDA071910	openfda.application_number
application number		ANDA071909	openfda.application_number
brand name		SODIUM IODIDE I 123	openfda.brand_name
generic name		SODIUM IODIDE I 123	openfda.generic_name
manufacturer name		Curium US LLC	openfda.manufacturer_name
ndc	package	69945-601-10	openfda.package_ndc
ndc	package	69945-602-20	openfda.package_ndc
ndc	product	69945-601	openfda.product_ndc
ndc	product	69945-602	openfda.product_ndc
ndc11	package	69945060220	derived:openfda.package_ndc
ndc11	package	69945060110	derived:openfda.package_ndc
spl id		24b19127-9a67-0ddf-e063-6394a90ae0b5	id
spl set id		493fa2ab-4eb0-4434-9739-3079b2f0e272	set_id
unii		29UKX3A616	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Females of childbearing age and pediatric patients should not be studied unless the benefits anticipated from the performance of the test outweigh the possible risk of exposure to the amount of ionizing radiation associated with the test.

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTIONS Although rare, reactions associated with the administration of sodium iodide isotopes for diagnostic use include, in decreasing order of frequency, nausea, vomiting, chest pain, tachycardia, itching skin, rash and hives.

Reported adverse events (FAERS/openFDA)#

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