Scandium iodatum

Manufacturer: Hahnemann Laboratories, Inc.
Effective date: 2017-11-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:08:58

Label at a glance#

ProductScandium iodatum

Active ingredientSCANDIUM IODIDE

Label structure1 sections

Label contents#

Full prescribing information#

Single label image contains content for sections 1-17.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

img

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Code 128	00000		Scand-iod.jpg, 5e83b829-7535-4f25-e053-2991aa0a7b3a.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63545-694-01	2020-01-31	C162847	48780-1	9d75b9d1-1db2-f424-e053-dadaa90a57ce	5e80d6f0-aca7-5600-e053-2a91aa0a05c8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63545-694-01	Scandium iodatum	240 [hp_C] in 1 VIAL, GLASS	PELLET	240		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63545-694	SCANDIUM IODATUM PELLET [HAHNEMANN LABORATORIES, INC.]	1	Legacy NDC, 1 package rows	20171121_5e80d6f0-aca7-5600-e053-2a91aa0a05c8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Scandium iodatum
SUCROSE
SCANDIUM IODIDE
SCANDIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63545-694	63545-694-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
SCANDIUM IODIDE	QVJ18SK04T	ACTIB

Source Document#

Source XML

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
5e80d6f0-aca8-5600-e053-2a91aa0a05c8			5e80d6f0-aca7-5600-e053-2a91aa0a05c8	2017-11-21		Exact identifier spl id: 5e80d6f0-aca8-5600-e053-2a91aa0a05c8 spl set id: 5e80d6f0-aca7-5600-e053-2a91aa0a05c8

Reported adverse events (FAERS/openFDA)#

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