HELIUM

Manufacturer
Acetylene Oxygen Company
Effective date
2011-04-27
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:51:34

Label at a glance#

ProductHELIUM
Active ingredientHELIUM
Label structure1 sections

Label contents#

Full prescribing information#

HELIUM HP USP SHOULDER LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HELIUM COMPRESSED USP UN 1046 NON-FLAMMABLE  37580   (R  06/05)

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 SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN.

CAUTION; HIGH PRESSURE GAS.  CAN CAUSE RAPID SUFFOCATION.  STORE AND USE WITH ADEQUATE VENTILATION.  USE EQUIPMENT RATED FOR CYLINDER PRESSURE. USE A BACK FLOW PREVENTIVE VALVE AFTER EACH USE. CYLINDER TEMPERATURE SHOULD NOT EXCEED 52C (125 F)  CLOSE VALVE AFTER EACH USE AND WHEN EMPTY.  USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS)

INHALING HELIUM TO ALTER VOICE MAY PROVE TO BE FATAL AND SHOULD NOT BE PERMITTED.

FIRST AID: IF INHALED, REMOVE TO FRESH AIR.  IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION. IF BREATHING IS DIFFICULT, GIVE OXYGEN. CALL A PHYSICIAN

CAS: 7440-59-7    DO NOT REMOVE THIS PRODUCT LABEL

CONTENTS______ LITERS _______CU.FT

HP HELIUM SHOULDER LABELHP HELIUM SHOULDER LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10006-008HELIUM GAS [ACETYLENE OXYGEN COMPANY]1Legacy NDC20110428_8c473d18-b656-4e00-8fbc-6e1128d41254.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HELIUMACTIVE INGREDIENT206GF3GB411
HELIUMACTIVE MOIETY206GF3GB411

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10006-00810006-008-01, 10006-008-02, 10006-008-03, 10006-008-04, 10006-008-05, 10006-008-06

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
NameUNIIKind
HELIUM206GF3GB41ACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2bb26a23-f775-4ae4-8575-1a8959a7b4e38c473d18-b656-4e00-8fbc-6e1128d412542026-01-20Exact identifier
spl set id: 8c473d18-b656-4e00-8fbc-6e1128d41254

Reported adverse events (FAERS/openFDA)#

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