FDA.reportPublic FDA data

HELIUM

Manufacturer
Air Source Industries Inc
Effective date
2024-10-06
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-05-31 21:13:46

Label at a glance#

ProductHELIUM
Active ingredientHELIUM
Label structure1 sections

Label contents#

Full prescribing information#

HELIUM COMPRESSED Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HELIUM COMPRESSED USP UN 1046

E15 A Air Source Industries, Inc.

          3976 CHERRY AVE., LONG BEACH, CA 90807

In CA (800) 295-4271 (562) 426-4017     AS-4

NON-FLAMMABLE GAS 2

WARNING: Administration of Helium may be hazardous or contraindicated. For use only 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 hazards, contraindications, and side effects and the precautions to be taken.

WARNING:CONTAINSGAS UNDER PRESSURE; MAT EXPLODEIF HEATED. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Use a back flow prevention device in the piping. Use only with equipment rated for cylinder pressure. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52°C (125°F). Read and follow the Safety Data Sheet (SDS) before use. FIRST AID:  IF INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention.

CAS: 7440-59-7 DO NOT REMOVE THIS PRODUCT LABEL

AirSource HeliumAirSource Helium

AirSource HeliumAirSource Helium

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
310693helium 99 % Gas for InhalationPSN12
310693helium 99 % Gas for InhalationSCD12

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10167-300-01HELIUM610 L in 1 CYLINDERGAS61012
10167-300-02HELIUM5800 L in 1 CYLINDERGAS580012
10167-300-03HELIUM6160 L in 1 CYLINDERGAS616012
10167-300-04HELIUM161 L in 1 CYLINDERGAS16112
10167-300-05HELIUM166 L in 1 CYLINDERGAS16612
10167-300-06HELIUM370 L in 1 CYLINDERGAS37012
10167-300-07HELIUM2780 L in 1 CYLINDERGAS278012
10167-300-08HELIUM1557 L in 1 CYLINDERGAS155712

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10167-300HELIUM GAS [AIR SOURCE INDUSTRIES INC]12Current NDC, Legacy NDC, 8 package rows20241008_7d1d5963-8b7f-4d8d-807a-6b9f896c7171.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
10167-30010167-300-01, 10167-300-02, 10167-300-03, 10167-300-04, 10167-300-05, 10167-300-06, 10167-300-07, 10167-300-08

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

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

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
HELIUMHELIUMAir Source Industries Inc7d1d5963-8b7f-4d8d-807a-6b9f896c71712024-10-06Exact identifier
ndc (package): 10167-300-01
ndc (package): 10167-300-06
ndc (package): 10167-300-05
ndc (package): 10167-300-08
ndc (package): 10167-300-04
ndc (package): 10167-300-07
ndc (package): 10167-300-03
ndc (package): 10167-300-02
ndc (product): 10167-300
ndc11 (package): 10167030006
ndc11 (package): 10167030005
ndc11 (package): 10167030007
ndc11 (package): 10167030003
ndc11 (package): 10167030004
ndc11 (package): 10167030008
ndc11 (package): 10167030002
ndc11 (package): 10167030001
spl id: bbffc3c2-c49f-4215-8e74-0a2e7a92e3cd
spl set id: 7d1d5963-8b7f-4d8d-807a-6b9f896c7171

Reported adverse events (FAERS/openFDA)#

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