Helium
- Manufacturer
- Matheson Tri-Gas, Inc.
- Effective date
- 2026-10-16
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 19
- Source
- daily-update
- Hydrated at
- 2026-10-20 03:06:34
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
HELIUM, COMPRESSED USP
UN1046
DO NOT REMOVE THIS PRODUCT LABEL.
CONTENTS: LTRS: CU.FT
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 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. WARNING: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Obtain, read and follow all safety instructions before use. Use and store only outdoors or in a well-ventilated place. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Never put cylinders into unventilated areas of passenger vehicles. Do not open valve until connected to equipment prepared for use. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Nippon Sanso Matheson, Inc. Safety Data Sheet (SDS) before use. FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical help if you feel unwell. Return with 25 psig. CAS: 7440-59-7
NIPPON SANSO
NIPPON SANSO MATHESON, INC.
909 LAKE CAROLYN PKWY SUITE 1100
IRVING, TEXAS 75039 1-800-416-2505
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
HELIUM, COMPRESSED USP
UN1046
DO NOT REMOVE THIS PRODUCT LABEL.
CONTENTS: LTRS: CU. FT.
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 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. WARNING: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Obtain, read and follow all safety instructions before use. Use and store only outdoors or in a well-ventilated place. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Never put cylinders into unventilated areas of passenger vehicles. Do not open valve until connected to equipment prepared for use. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Nippon Sanso Matheson, Inc. Safety Data Sheet (SDS) before use. FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical help if you fell unwell. Return with 25 psig.
CAS: 7440-59
NIPPON SANSO
NIPPON SANSO MATHESON, INC.
909 LAKE CAROLYN PKWY SUITE 1100
IRVING, TEXAS 75039 1-800-416-2505
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Helium | ACTIVE INGREDIENT | 206GF3GB41 | 3 | |
| HELIUM | ACTIVE MOIETY | 206GF3GB41 | 3 |
Products#
Every source-derived product name is available through these pages.
- Helium
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55037-501 | 55037-501-01, 55037-501-02, 55037-501-03, 55037-501-04, 55037-501-05, 55037-501-06, 55037-501-07, 55037-501-08, 55037-501-09, 55037-501-10, 55037-501-11, 55037-501-12, 55037-501-13, 55037-501-14, 55037-501-15, 55037-501-16, 55037-501-17, 55037-501-18, 55037-501-19 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HELIUM | 206GF3GB41 | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 18 | 2025-12-02 | full-release | 2026-05-31 21:48:00 |
Orange Book application contexts#
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 44ffa5d3-de0e-2611-e063-6294a90a156d | 12440277-7160-4e8e-99e2-39e4b4a2c866 | 2025-12-02 | 12440277-7160-4e8e-99e2-39e4b4a2c866 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

