Helium

Manufacturer
Airgas East, Inc.
Effective date
2010-06-23
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:09:08

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 GAS  2            836580 (12/04)
Rx only. CAUTION: Federal law prohibits dispensing without prescription. WARNING: Administration of Helium may be hazardous or contraindicated. For use only by or under 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 equipment rated for cylinder pressure. Use a back flow preventive device in the piping. Cylinder temperatures should not exceed 52C (125F). 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     AIRGAS EAST, Inc.  Salem, NH  03079 (800) 562-3815heliumhelium

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
347675helium 99.9 % Gas for InhalationPSN2
347675helium 99.9 % Gas for InhalationSCD2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
25543-011-012019-10-21C16284748780-1956f9ecf-dc23-621f-e053-dbdaa90a74adhelium
25543-011-022019-10-21C16284748780-1956f9ecf-dc23-621f-e053-dbdaa90a74adhelium
25543-011-032019-10-21C16284748780-1956f9ecf-dc23-621f-e053-dbdaa90a74adhelium
25543-011-042019-10-21C16284748780-1956f9ecf-dc23-621f-e053-dbdaa90a74adhelium
25543-011-052019-10-21C16284748780-1956f9ecf-dc23-621f-e053-dbdaa90a74adhelium

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
25543-011-01Helium300 L in 1 CYLINDERGAS3002
25543-011-02Helium500 L in 1 CYLINDERGAS5002
25543-011-03Helium3100 L in 1 CYLINDERGAS31002
25543-011-04Helium6910 L in 1 CYLINDERGAS69102
25543-011-05Helium8240 L in 1 CYLINDERGAS82402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25543-011HELIUM GAS [AIRGAS EAST, INC.]2Legacy NDC, 5 package rows20100719_5fcaa2df-27a6-4533-886e-268393925517.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HeliumACTIVE INGREDIENT206GF3GB412
HeliumACTIVE MOIETY206GF3GB412

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
25543-01125543-011-01, 25543-011-02, 25543-011-03, 25543-011-04, 25543-011-05

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
e310afbc-50fa-4883-921e-792b38c6c3915fcaa2df-27a6-4533-886e-2683939255172010-06-23Exact identifier
spl id: e310afbc-50fa-4883-921e-792b38c6c391
spl set id: 5fcaa2df-27a6-4533-886e-268393925517

Reported adverse events (FAERS/openFDA)#

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