Oxygen Helium Mixture 20/80

Manufacturer
AGL Inhalation Therapy Co.
Effective date
2026-01-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 22:06:35

Label at a glance#

ProductOxygen Helium Mixture 20/80
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AGL Certified ISO 9001:2008 Inhalation Therapy Co. CLIFTON, NJ 07015 973-478-5100
NON-FLAMMABLE GAS 2 OXYDIZER 5.1
Compressed gas, oxidizing, n.o.s. (Oxygen, Helium) UN1956 Part # K2MOH Medical Gas Mixture 20% Oxygen, USP CAS: 7782-44-7 Balance Helium, USP CAS: 7440-59-7
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. MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. Do not handle until all safety precautions have been read and understood. Keep and store away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or in a well-ventilated place. Use a back flow preventive device in the piping. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Open valve slowly. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52 degrees C (125 degrees F). Read and follow the Safety Data Sheet before use. FIRST AID: IF ACCIDENTALLY INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention. DO NOT REMOVE THIS PRODUCT LABEL For Medical Use Only. Label # AGL-8-D-124-4 01/21/16 Ver. 3.67 Volume: 4910 Liters AGL 600 Rt. 46 W CLIFTON, N.J., 07015 helium oxygen eighty twentyhelium oxygen eighty twenty

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
413101oxygen 20 % Gas for InhalationPSN14
413101oxygen 20 % Gas for InhalationSCD14
413101nitrogen (inactive) 80 % / oxygen 20 % Gas for InhalationSY14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17575-192-01Oxygen Helium Mixture 20/804554 L in 1 CYLINDERGAS455414
17575-192-02Oxygen Helium Mixture 20/80500 L in 1 CYLINDERGAS50014
17575-192-03Oxygen Helium Mixture 20/804910 L in 1 CYLINDERGAS491014

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17575-19217575-192-01, 17575-192-02, 17575-192-03

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.

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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
Oxygen Helium Mixture 20/80OXYGEN HELIUM MIXTURE 20/80AGL Inhalation Therapy Co.e5f7f27b-5c9d-47f3-8312-641cb8b3ffd12026-01-01Exact identifier
ndc (package): 17575-192-03
ndc (package): 17575-192-02
ndc (package): 17575-192-01
ndc (product): 17575-192
ndc11 (package): 17575019201
ndc11 (package): 17575019203
ndc11 (package): 17575019202
spl id: 41c377c4-ee36-0c64-e063-6394a90a6cb7
spl set id: e5f7f27b-5c9d-47f3-8312-641cb8b3ffd1

Reported adverse events (FAERS/openFDA)#

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