Oxygen Helium Mixture

Manufacturer
Aero All Gas Company
Effective date
2017-12-18
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:25:06

Label at a glance#

ProductOxygen Helium Mixture
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COMPRESSED GAS, N.O.S. (80% HELIUM USP, 20% OXYGEN USP) UN1956 NON-FLAMMABLE GAS 2
Rx only 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.
DANGER: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Do not handle until all safety precautions have been read and understood. Avoid breathing gas. 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. when Protect from sunlight when ambient temperature exceeds 52 degrees C (125 degrees F). Read and follow the Safety Data Sheet.
FIRST AID: IF ACCIDENTALLY INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention.
CAS HELIUM 7440-59-7 OXYGEN 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.
ALL-GAS THE AERO ALL-GAS COMPANY 3150 MAIN ST. . HARTFORD, CT 06120 (860) 278-AERO (2376) he80ox20he80ox20

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
413101oxygen 20 % Gas for InhalationPSN1
413101oxygen 20 % Gas for InhalationSCD1
413101nitrogen (inactive) 80 % / oxygen 20 % Gas for InhalationSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10014-009-032020-01-31C16284748780-19d75b9cf-eb1c-f424-e053-dadaa90a57ceO2 20 HE 80 MIX
10014-009-042020-01-31C16284748780-19d75b9cf-eb1c-f424-e053-dadaa90a57ceO2 20 HE 80 MIX
10014-009-052020-01-31C16284748780-19d75b9cf-eb1c-f424-e053-dadaa90a57ceO2 20 HE 80 MIX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10014-009-03Oxygen Helium Mixture425 L in 1 CYLINDERGAS4251
10014-009-04Oxygen Helium Mixture705 L in 1 CYLINDERGAS7051
10014-009-05Oxygen Helium Mixture7108 L in 1 CYLINDERGAS71081

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10014-009OXYGEN HELIUM MIXTURE GAS [AERO ALL GAS COMPANY]1Legacy NDC, 3 package rows20171221_60ced542-19d3-57d5-e053-2a91aa0a49be.zip

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
10014-00910014-009-03, 10014-009-04, 10014-009-05

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
HELIUM206GF3GB41IACT
OXYGENS88TT14065ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
60ced542-19d4-57d5-e053-2a91aa0a49be60ced542-19d3-57d5-e053-2a91aa0a49be2017-12-18Exact identifier
spl id: 60ced542-19d4-57d5-e053-2a91aa0a49be
spl set id: 60ced542-19d3-57d5-e053-2a91aa0a49be

Reported adverse events (FAERS/openFDA)#

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