Helium

Manufacturer: Praxair, Puerto Rico Inc.
Effective date: 2022-12-27
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 15
Source: full-release
Hydrated at: 2026-05-31 20:45:50

Label at a glance#

ProductHelium

Active ingredientHELIUM

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
310693	helium 99 % Gas for Inhalation	PSN	15
310693	helium 99 % Gas for Inhalation	SCD	15

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11324-005-01	2024-01-30	C162847	48780-1	1030e365-5188-111a-e063-dadaa90a10e2	Helium USP Gurabo

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
11324-005-01	Helium	113 L in 1 CYLINDER	GAS	113		15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11324-005	HELIUM GAS [PRAXAIR, PUERTO RICO INC.]	15	Legacy NDC, 1 package rows	20221228_c00cd64f-8736-4f9c-ba02-c9d49b7344df.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
HELIUM	ACTIVE INGREDIENT	206GF3GB41	1
HELIUM	ACTIVE MOIETY	206GF3GB41	1

Products#

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

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

Helium

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
11324-005	11324-005-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
HELIUM	206GF3GB41	ACTIB

Source Document#

Source XML · Source PDF

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
f0d422db-7e59-699a-e053-2a95a90a44bc			c00cd64f-8736-4f9c-ba02-c9d49b7344df	2022-12-27		Exact identifier spl id: f0d422db-7e59-699a-e053-2a95a90a44bc spl set id: c00cd64f-8736-4f9c-ba02-c9d49b7344df

Reported adverse events (FAERS/openFDA)#

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