Helium
- Manufacturer
- Medical-technical Gases, Inc.
- Effective date
- 2023-10-18
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:23:58
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
HELIUM, COMPRESSED USP
UN1046
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. 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 preventive 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
MEDICAL-TECHNICAL GASES, INC.
8 EXECUTIVE PARK DRIVE NORTH BILLERICA, MA 01862
TEL. 800 FINE GAS FAX (781) 395-9098
www.medtechgases.com
Products#
Every source-derived product name is available through these pages.
- Helium
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10736-020 | 10736-020-01, 10736-020-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HELIUM | 206GF3GB41 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 2b492e8b-1baa-3ca8-e063-6394a90abaf0 | b8cea45c-16b2-3daa-e053-2a95a90aa942 | 2025-01-09 | b8cea45c-16b2-3daa-e053-2a95a90aa942 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
