Xenon

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: Xenon
Generic name: XENON XE-133
Manufacturer: Shine Spect USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 74f95143-d3b4-4e69-b200-e09bf811516b
SPL ID: a5956751-131b-4a35-9b1f-e3ec97585dc7
Version: 2
Effective date: 2026-09-10
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:36

Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	017284	derived:openfda.application_number
application number		NDA017284	openfda.application_number
brand name		Xenon	openfda.brand_name
generic name		XENON XE-133	openfda.generic_name
manufacturer name		Shine Spect USA, LLC	openfda.manufacturer_name
ndc	package	87333-128-21	openfda.package_ndc
ndc	package	87333-127-15	openfda.package_ndc
ndc	package	87333-128-25	openfda.package_ndc
ndc	package	87333-127-11	openfda.package_ndc
ndc	product	87333-127	openfda.product_ndc
ndc	product	87333-128	openfda.product_ndc
ndc11	package	87333012825	derived:openfda.package_ndc
ndc11	package	87333012711	derived:openfda.package_ndc
ndc11	package	87333012715	derived:openfda.package_ndc
ndc11	package	87333012821	derived:openfda.package_ndc
spl id		a5956751-131b-4a35-9b1f-e3ec97585dc7	id
spl set id		74f95143-d3b4-4e69-b200-e09bf811516b	set_id
unii		X3P9A5HNYF	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: Xenon Xe 133 Gas delivery systems, i.e., respirators or spirometers, and associated tubing assemblies must be leakproof to avoid loss of radioactivity into the environs not specifically protected by exhaust systems. Xenon Xe 133 adheres to some plastics and rubber and should not be allowed to stand in tubing or respirator containers. The unrecognized loss of radioactivity from the dose for administration may render the study non-diagnostic. The vial stopper contains dry natural rubber latex and may cause allergic reactions in providers or patients who are sensitive to latex.

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: Adverse reactions related to the use of this agent have not been reported to date.

Reported adverse events (FAERS/openFDA)#

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