helium

Manufacturer
AGL Inhalation Therapy Co.
Effective date
2026-10-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
17
Source
daily-update
Hydrated at
2026-11-03 06:23:04

Label at a glance#

ProductHelium
Active ingredientHELIUM
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AGL
Auto Gas Light
HELIUM,
COMPRESSED
USP
U.N. 1046
AGL-8-D-103-2  (11/09)
NON-FLAMMABLE GAS     2
Rx only. 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 of administration of helium and is familiar with indications, dosages and 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. User shall secure cylinder in use and in storage. Use in upright position. Use equipment rated for cylinder pressure. Use a back flow preventive device in the piping. Cylinder temperature should not exceed 52 degrees C (125 degrees F). Close valve after each use and when empty. Keep valve protective cap in place when not in use, if so equipped. Use in accordance with the Material Safety Data Sheet (MSDS). Inhaling Helium to alter 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
DO NOT REMOVE THIS PRODUCT LABEL
RETURN WITH 25 PSIG.
AGL Inhalation Therapy Co. Clifton, NJ 07015
973-478-5100
973-478-5000
Pressure:          PSIG at 70 degrees F.
Size
Contents      liters heliumhelium

FDA-Initiated Inactive NDC Indexing#

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
17575-00517575-005-01, 17575-005-02, 17575-005-03, 17575-005-04, 17575-005-05, 17575-005-06

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
162026-03-02full-release2026-05-31 22:09:18
152026-01-01monthly-update2026-06-03 17:57:46

Orange Book application contexts#

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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
4cc19ab7-134d-fce9-e063-6294a90ac0f5b309a459-c8bc-4ac3-a4e2-3989a63be8a92026-03-02Exact identifier
spl set id: b309a459-c8bc-4ac3-a4e2-3989a63be8a9

Reported adverse events (FAERS/openFDA)#

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