FDA.reportPublic FDA data

Helium/Oxygen Mixture 80/20

Manufacturer
General Air Service & Supply Co
Effective date
2010-12-22
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:10:53

Label at a glance#

ProductHelium/Oxygen Mixture 80/20
Active ingredientHelium, Oxygen
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPRESSED GAS, OXIDIZING, N.O.S.    (     % OXYGEN USP    %HELIUM USP) UN3156
NON-FLAMMABLE GAS 2     OXIDIZER 5.1   34499 (11/05)
OXYGEN CONTENT OVER 23.5 %
Rx only. CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. WARNING: Administration of this gas mixture 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 gas mixtures, 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. CAUTION: HIGH PRESSURE OXDIZING GAS. VIGOROUSLY ACCELERATES COMBUSTION. Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Use a back flow preventive device in the piping. Cylinder temperature should not exceed 52C (125F). Close valve after each use and when empty. Use in accordance with the Material Safety Data Sheet (MSDS). FIRST AID: IF INHALED,  remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician. CAS: OXYGEN  7782-44-7    HELIUM 7440-59-7    DO NOT REMOVE THIS PRODUCT LABEL.   
FILLED and INPSECTED BY GENERAL AIR SERVICE and SUPPLY DENVER, CO 80204labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
542169helium 80 % / oxygen 20 % Gas for InhalationPSN1
542169helium 80 % / oxygen 20 % Gas for InhalationSCD1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21220-127-012019-10-29C16284748780-1960f7f55-c3b3-8e05-e053-dbdaa90a074aHelium/Oxygen Mixture 80/20
21220-127-022019-10-29C16284748780-1960f7f55-c3b3-8e05-e053-dbdaa90a074aHelium/Oxygen Mixture 80/20

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21220-127-01Helium/Oxygen Mixture 80/207108 L in 1 CYLINDERGAS71081
21220-127-02Helium/Oxygen Mixture 80/20708 L in 1 CYLINDERGAS7081

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21220-127HELIUM/OXYGEN MIXTURE 80/20 GAS [GENERAL AIR SERVICE & SUPPLY CO]1Legacy NDC, 2 package rows20101223_92c68434-5df9-4a45-9db2-3f29cb46424c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HeliumACTIVE INGREDIENT206GF3GB411
OxygenACTIVE INGREDIENTS88TT140651
HeliumACTIVE MOIETY206GF3GB411
OxygenACTIVE MOIETYS88TT140651

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21220-12721220-127-01, 21220-127-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Helium206GF3GB41ACTIB
OxygenS88TT14065ACTIB

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
36e702f1-4f5d-4286-a650-3d0ccbe2f16d92c68434-5df9-4a45-9db2-3f29cb46424c2010-12-22Exact identifier
spl id: 36e702f1-4f5d-4286-a650-3d0ccbe2f16d
spl set id: 92c68434-5df9-4a45-9db2-3f29cb46424c

Reported adverse events (FAERS/openFDA)#

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