Oxygen

Manufacturer
CHI National Home Care dba MercyOne Des Moines Home Respiratory Care
Effective date
2019-12-16
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 20:30:41

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Liquid LabelLiquid Label

OXYGEN,

REFRIGERATED LIQUID

USP

UN 1073

CONTENTS: LITERS

ALWAYS KEEP CONTAINER IN UPRIGHT POSITION

WARNING:

DO NOT CHANGE OR FORCE FIT CONNECTIONS

EXTREMELY COLD OXIDIZING LIQUID AND GAS UNDER PRESSURE

VIGOROUSLY ACCELERATES COMBUSTION

NO SMOKING IN THE PRESENCE OF OXYGEN OR A FIRE MAY RESULT

COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE

ON IGNITION OR IMPACT.

CAN CAUSE SEVERE FROSTBITE.

Keep oil, grease, and combustibles away.

Use only with equipment cleaned for oxygen service.

Store and use with adequate ventilation.

Do not get liquid in eyes, on skin or clothing.

For liquid withdrawal, wear face shield and gloves.

Do not drop. Use suitable hand truck for container movement.

Container temperatures should not exceed 52 degrees C ( 125 degrees F).

Close valve after each use and when empty.

Use a back flow preventive device in the piping.

Use in accordance with the Material Safety Data Sheet (MSDS).


FIRST AID:



IN CASE OF FROSTBITE, obtain medical treatment immediately.



WARNING:



For emergency use only when administered by properly trained

personnel for oxygen deficiency 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. Use only with pressure reducing equipment

and apparatus designed for oxygen. Do not attempt to use on

patients who have stopped breathing, unless used in conjunction

with resuscitative equipment.



Produced by Air Liquefaction



DO NOT REMOVE THIS PRODUCT LABEL.






DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN3
312172oxygen 99 % Gas for InhalationSCD3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52726-4083-12021-01-29C16284748780-1ba0f9c33-53b7-a910-e053-dadaa90a0b85Oxygen
52726-4083-22021-01-29C16284748780-1ba0f9c33-53b7-a910-e053-dadaa90a0b85Oxygen
52726-4083-32021-01-29C16284748780-1ba0f9c33-53b7-a910-e053-dadaa90a0b85Oxygen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52726-4083-1Oxygen21 L in 1 DEWARGAS213
52726-4083-2Oxygen31 L in 1 DEWARGAS313
52726-4083-3Oxygen41 L in 1 DEWARGAS413

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52726-4083OXYGEN GAS [CHI NATIONAL HOME CARE DBA MERCYONE DES MOINES HOME RESPIRATORY CARE]3Legacy NDC, 3 package rows20191217_636e12b1-f99e-4bfc-8255-1e35120fe25a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OxygenACTIVE INGREDIENTS88TT140651
OxygenACTIVE MOIETYS88TT140651

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
52726-408352726-4083-1, 52726-4083-2, 52726-4083-3

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

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
99d529de-e342-18f3-e053-2a95a90a4ebc636e12b1-f99e-4bfc-8255-1e35120fe25a2019-12-16Exact identifier
spl id: 99d529de-e342-18f3-e053-2a95a90a4ebc
spl set id: 636e12b1-f99e-4bfc-8255-1e35120fe25a

Reported adverse events (FAERS/openFDA)#

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