Helium

Manufacturer
Airgas-West, Inc.
Effective date
2010-05-25
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:09:13

Label at a glance#

ProductHelium
Active ingredientHelium
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HELIUM, COMPRESSED USP
 UN1046
DO NOT REMOVE THIS PRODUCT LABEL.
NON-FLAMMABLE 2     
836580 (12/04)
Rx only.
CAUTION: Federal law prohibits dispensing without a prescription. WARNING: Administration of Helium may be hazardous or contraindicated. For use by or under the supervision of a licensed practitioner who is experienced in the use and administration of Helium and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects, and the precautions to be taken.

CAUTION: HIGH PRESSURE GAS. CAN CAUSE RAPID SUFFOCATION. Store and use with adequate ventilation. Use only with equipment rated for cylinder pressure. Use a back flow preventive device in the piping. Cylinder temperature should not exceed 52oC(125oF). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). Inhaling Helium to alter the voice may prove fatal and should not be permitted.
    
 FIRST AID:   IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.     CAS: 7440-59-7

AIRGAS PURITAN MEDICAL Distributed By:  Airgas West, Inc. Lakewood, CA 90712 (562) 497-1991heliumhelium

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
997972helium 99.2 % Gas for InhalationPSN1
997972helium 99.2 % Gas for InhalationSCD1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10678-004-012019-10-21C16284748780-1956f9ecf-d63e-621f-e053-dbdaa90a74adhelium
10678-004-022019-10-21C16284748780-1956f9ecf-d63e-621f-e053-dbdaa90a74adhelium
10678-004-032019-10-21C16284748780-1956f9ecf-d63e-621f-e053-dbdaa90a74adhelium
10678-004-042019-10-21C16284748780-1956f9ecf-d63e-621f-e053-dbdaa90a74adhelium

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10678-004-01Helium2265 L in 1 CYLINDERGAS22651
10678-004-02Helium3539 L in 1 CYLINDERGAS35391
10678-004-03Helium5663 L in 1 CYLINDERGAS56631
10678-004-04Helium8495 L in 1 CYLINDERGAS84951

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10678-004HELIUM GAS [AIRGAS-WEST, INC.]1Legacy NDC, 4 package rows20100719_8b9bf8cf-417c-4925-90f9-d89e1bc25d13.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HeliumACTIVE INGREDIENT206GF3GB411
HeliumACTIVE MOIETY206GF3GB411

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10678-00410678-004-01, 10678-004-02, 10678-004-03, 10678-004-04

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
NameUNIIKind
Helium206GF3GB41ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
30a834fa-7c4e-4b5c-9035-523b420350568b9bf8cf-417c-4925-90f9-d89e1bc25d132010-05-25Exact identifier
spl id: 30a834fa-7c4e-4b5c-9035-523b42035056
spl set id: 8b9bf8cf-417c-4925-90f9-d89e1bc25d13

Reported adverse events (FAERS/openFDA)#

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