FDA.reportPublic FDA data

OXYGEN

Manufacturer
Air Liquide America L.P.
Effective date
2018-09-28
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 20:26:30

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

OXYGEN REFRIGERATED LIQUID USP Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN,
REFRIGERATED
LIQUID
USP

UN1073

OXYGEN  2

DANGER: CONTAINS REFRIGERATED GAS: MAY CAUSE CRYOGENIC BURNS OR INJURY. MAY CAUSE OR INTENSIFY FIRE: OXIDIZER. COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT.

Do not get into eyes, on skin, or on clothing. Keep valves and fittings free from grease and oil. Do not smoke. In case of fire: Stop leak if safe to do so. Avoid spills. Do not walk or roll equipment over spills. Use and store only outdoors or in a well-ventilated place. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Wear cold insulating gloves/face shield/eye protection. Do not drop. Use suitable hand truck for container movement. Close valve after each use and when empty. Use a back-flow preventive device in the piping. Do not handle until all safety precautions have been read and understood. Use only with equipment cleaned for oxygen service. Keep/store away from clothing and other combustible materials. Always keep container in upright position. DO NOT change or force fit connections. Read and follow the Safety Data Sheet (SDS) before use.

FIRST AID: IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical attention.

WARNING: For emergency use only when administered by properly trained personnel for oxygen deficient and resuscitation. For all other medical applications Rx only.

Uninterrupted use of high concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of arterial blood, may be harmful. Do not attempt to use on patients who have stopped breathing unless used in conjunction with resuscitative equipment.

Keep out of reach of children.

Federal law required that this container be refilled with Oxygen USP only by establishments registered as a drug manufacture in accordance with the Federal Food, Drug, and Cosmetic Act.

DO NOT REMOVE THIS PRODUCT LABEL

CAS: 7782-44-7

AIRGAS® Healthcare
an Air Liquide Company
AIRGAS USA, LLC
Radnor, PA 19087-5283

Safety Data Sheets available at www.airgas.com

OXYGEN REFRIGERATED LabelOXYGEN REFRIGERATED Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN4
312172oxygen 99 % Gas for InhalationSCD4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10671-011-422020-01-31C16284748780-19d75b9d0-37b7-f424-e053-dadaa90a57ce660f8036-ebbb-4990-bacb-23b9a80c2927
10671-011-432020-01-31C16284748780-19d75b9d0-37b7-f424-e053-dadaa90a57ce660f8036-ebbb-4990-bacb-23b9a80c2927
10671-011-442020-01-31C16284748780-19d75b9d0-37b7-f424-e053-dadaa90a57ce660f8036-ebbb-4990-bacb-23b9a80c2927
10671-011-452020-01-31C16284748780-19d75b9d0-37b7-f424-e053-dadaa90a57ce660f8036-ebbb-4990-bacb-23b9a80c2927

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10671-011-42OXYGEN160 L in 1 CYLINDERGAS1604
10671-011-43OXYGEN180 L in 1 CYLINDERGAS1804
10671-011-44OXYGEN230 L in 1 CYLINDERGAS2304
10671-011-45OXYGEN40 L in 1 CYLINDERGAS404

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10671-011OXYGEN GAS [AIR LIQUIDE AMERICA L.P.]4Legacy NDC, 4 package rows20180929_660f8036-ebbb-4990-bacb-23b9a80c2927.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OXYGENACTIVE INGREDIENTS88TT140653
OXYGENACTIVE MOIETYS88TT140653

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
10671-01110671-011-42, 10671-011-43, 10671-011-44, 10671-011-45

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
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
657d3063-1ef1-42ab-8d1b-1b40a616a77b660f8036-ebbb-4990-bacb-23b9a80c29272018-09-28Exact identifier
spl id: 657d3063-1ef1-42ab-8d1b-1b40a616a77b
spl set id: 660f8036-ebbb-4990-bacb-23b9a80c2927

Reported adverse events (FAERS/openFDA)#

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