Helium

Manufacturer: General Air Service & Supply Co
Effective date: 2022-10-14
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 10
Source: legacy-cache
Hydrated at: 2026-08-01 21:51:37

Label at a glance#

ProductHelium

Active ingredientHELIUM

Label structure1 sections

Contacts and useful links#

PhoneLabel contact303-892-7003

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 CUASE 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.
FILLED & INSPECTED BY
GENERAL AIR SERVICE & SUPPLY
1105 ZUNI ST
DENVER, CO 80204
303-892-7003 helium

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Helium	ACTIVE INGREDIENT	206GF3GB41	1
Helium	ACTIVE MOIETY	206GF3GB41	1

Products#

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Helium

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
21220-121	21220-121-01, 21220-121-02

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

Orange Book application contexts#

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openFDA label cross-check#

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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
eb5603bb-087e-30bb-e053-2995a90a4b71			a3c269d8-e7fa-438c-b05e-dc77a48f23a0	2022-10-18		Exact identifier spl set id: a3c269d8-e7fa-438c-b05e-dc77a48f23a0

Reported adverse events (FAERS/openFDA)#

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