HELIUM

Manufacturer: Norco, Inc.
Effective date: 2025-08-31
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 8
Source: full-release
Hydrated at: 2026-05-31 21:41:39

Label at a glance#

ProductHELIUM

Active ingredientHELIUM

Label structure1 sections

Contacts and useful links#

PhoneLabel contact208-336-1643

Label contents#

Full prescribing information#

HELIUM COMPRESSED USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Helium
Compressed
USP
UN1046 ((RK-20) XXXXXXR

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. Protect from sunlight when ambient temperature exceeds 52º C (125º F).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. Do not open valve until connected to equipment prepared for use. 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

Norco
1125 W. Amity Rd. • Boise, ID 83705
208-336-1643

CONTENTS

LTRS: __

CU.FT. __

helium compressed

res

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
310693	helium 99 % Gas for Inhalation	PSN	8
310693	helium 99 % Gas for Inhalation	SCD	8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
42602-002-01	HELIUM	595 L in 1 CYLINDER	GAS	595	8
42602-002-02	HELIUM	6202 L in 1 CYLINDER	GAS	6202	8
42602-002-03	HELIUM	368 L in 1 CYLINDER	GAS	368	8
42602-002-04	HELIUM	142 L in 1 CYLINDER	GAS	142	8
42602-002-05	HELIUM	1530 L in 1 CYLINDER	GAS	1530	8

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
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.

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

HELIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
42602-002	42602-002-01, 42602-002-02, 42602-002-03, 42602-002-04, 42602-002-05

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

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	Norco, Inc.	e1d2805c-1ede-4de5-b06e-f5cffc3ffd3c	2025-08-31		Exact identifier ndc (package): 42602-002-03 ndc (package): 42602-002-01 ndc (package): 42602-002-04 ndc (package): 42602-002-05 ndc (package): 42602-002-02 ndc (product): 42602-002 ndc11 (package): 42602000203 ndc11 (package): 42602000205 ndc11 (package): 42602000204 ndc11 (package): 42602000202 ndc11 (package): 42602000201 spl id: 98d996ba-6551-4cf7-b28d-088a76dcbccf spl set id: e1d2805c-1ede-4de5-b06e-f5cffc3ffd3c

Reported adverse events (FAERS/openFDA)#

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