Helium

Manufacturer: ILMO Products Company
Effective date: 2025-10-29
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-05-31 22:03:33

Label at a glance#

ProductHelium

Active ingredientHELIUM

Label structure1 sections

Contacts and useful links#

PhoneLabel contact217-245-2183

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.

ILMO products company

7 EASTGATE DRIVE

JACKSONVILLE, ILLINOIS 62650

217-245-2183 helium

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
310693	helium 99 % Gas for Inhalation	PSN	9
310693	helium 99 % Gas for Inhalation	SCD	9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51486-020-01	Helium	144.4 L in 1 CYLINDER	GAS	144.4	9
51486-020-02	Helium	623 L in 1 CYLINDER	GAS	623	9
51486-020-03	Helium	3201.39 L in 1 CYLINDER	GAS	3201.39	9
51486-020-04	Helium	957 L in 1 CYLINDER	GAS	957	9
51486-020-05	Helium	5689 L in 1 CYLINDER	GAS	5689	9

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

Helium

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51486-020	51486-020-01, 51486-020-02, 51486-020-03, 51486-020-04, 51486-020-05

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
Name	UNII	Kind
HELIUM	206GF3GB41	ACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
8	2025-04-02	full-release	2026-05-31 21:29:00

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Helium	HELIUM	ILMO Products Company	9aefb755-268a-1d8b-e053-2a95a90a1df7	2025-10-29		Exact identifier ndc (package): 51486-020-02 ndc (package): 51486-020-03 ndc (package): 51486-020-01 ndc (package): 51486-020-04 ndc (package): 51486-020-05 ndc (product): 51486-020 ndc11 (package): 51486002001 ndc11 (package): 51486002003 ndc11 (package): 51486002005 ndc11 (package): 51486002002 ndc11 (package): 51486002004 spl id: 424c9c8a-5805-0b5d-e063-6294a90ad8d2 spl set id: 9aefb755-268a-1d8b-e053-2a95a90a1df7

Reported adverse events (FAERS/openFDA)#

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