OXYGEN

Manufacturer
Isis Medical, Inc.
Effective date
2011-04-26
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:11:48

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

REFRIGERATED LIQUID OXYGEN REFRIGERATED LIQUID USP UN1073  OXYGEN 2

 ALWAYS KEEP CONTAINER IN UPRIGHT POSITION.  DO NOT CHANGE OR FORCE FIT CONNECTIONS. 

WARNING: FOR EMERGENCY USE ONLY WHEN ADMINISTERED BT 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 REDICING EQUIPMENT AND APPARATUS DESIGNED FOR OXYGEN. DO NOT ATTEMPT TO USE ON PATIENTS WHO HAVE STOPPED BREATING, UNLESS USED IN CONJUNCTION WITH RESUSCITATIVE EQUIPMENT.

PRODUCED BY AIR LIQUEFACTION.

WARNING:EXTREMELY COLD, OXIDIZING LIQUID AND GAS UNDER PRESSURE.  VIGOROUSLY ACCELERATES COMBUSTION. 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.  AVOID SPILLS.  DO NOT WALK OR ROLL EQUIPMENT OVER SPILLS.  CONTAINER TEMPERATURE SHOULD NOT EXCEED 52C (125 F)  CLOSE VALVE AFTER EACH USE AND WHEN EMPTY.  USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING.  USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS) 

FIRST AID: IN CASE OF FROSTBITE OBTAIN MEDICAL ATTENTION IMMEDIATELY.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

41533 (R10/04)

OXYGEN LIQUID LABEL
OXYGEN LIQUID LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN1
312172oxygen 99 % Gas for InhalationSCD1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76091-001-01OXYGEN160 L in 1 DEWARGAS1601
76091-001-02OXYGEN180 L in 1 DEWARGAS1801
76091-001-03OXYGEN176 L in 1 DEWARGAS1761
76091-001-04OXYGEN225 L in 1 DEWARGAS2251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76091-001OXYGEN GAS [ISIS MEDICAL, INC.]1Legacy NDC, 4 package rows20110428_57e2817e-ac86-4fea-a004-57af5fc1dfcb.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
76091-00176091-001-01, 76091-001-02, 76091-001-03, 76091-001-04

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
cfb1e46a-6a5a-40cd-ab80-0507876f500357e2817e-ac86-4fea-a004-57af5fc1dfcb2011-04-26Exact identifier
spl id: cfb1e46a-6a5a-40cd-ab80-0507876f5003
spl set id: 57e2817e-ac86-4fea-a004-57af5fc1dfcb

Reported adverse events (FAERS/openFDA)#

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