NDC 69208-003 - Sodium Iodide I-131

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 69208-003
Package NDCs from labels: 69208-003-15, 69208-003-25, 69208-003-35
Manufacturer: Radnostix, Inc.
Effective date: 2026-01-23
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sodium Iodide I-131 - Radnostix, Inc.	Radnostix, Inc.	2026-01-23	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69208-003	SODIUM IODIDE I-131 KIT [INTERNATIONAL ISOTOPES INC]	7	Unmatched	20240110_380e8e26-0625-4233-b36e-afb9f66e8a77.zip

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 2 of 2 · 23 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Miracle FootCream Lemon	UREA, GLYCERIN, ALOE, DISODIUM EDTA	Aloe Vera Korea Co.,Ltd.	db525c63-29fd-2033-e053-2995a90a56b9	2022-03-28	Warnings	Exact identifier unii: 7FLD91C86K
Sodium Phosphates	SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE	Fresenius Kabi USA, LLC	e6169d3b-39d2-47f9-8d5b-b53ec069a722	2021-07-23	Warnings, Adverse reactions	Exact identifier unii: 22ADO53M6F
Sodium Iodide I 131 Diagnostic	SODIUM IODIDE I 131	Jubilant DraxImage Inc., dba Jubilant Radiopharma	46b8d7ba-432d-d610-84f2-550bf9d0bae3	2020-08-25	Warnings, Adverse reactions	Exact identifier unii: 29VCO8ACHH

Reported adverse events (FAERS/openFDA)#

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