Oxygen, Refrigerated Liquid

Manufacturer
Airgas, Inc. | Tri-Med Medical Supplies, Inc | Airgas Usa, LLC
Effective date
2019-10-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-02 00:04:19

Label at a glance#

ProductOxygen, Refrigerated Liquid
Active ingredientOXYGEN
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN, REFRIGERATED LIQUID USP
UN 1073
CONTENTS: 40 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.
                        Avoid spills. Do not walk on or roll equipment over spills.
                        Container temperature should not exceed 52C (125F).
                        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 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.


CAS NO: 7782-44-7

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Tri-Med Medical Liquid Oxygen
Tri-Med Medical Liquid Oxygen

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OXYGENACTIVE INGREDIENTS88TT140656
OXYGENACTIVE MOIETYS88TT140656

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
25543-10025543-100-40

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#

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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
d82545a8-7290-1b47-e053-2995a90a3eea27cbc34c-33cf-453a-816b-6d3fdc9322d22022-02-16Exact identifier
spl set id: 27cbc34c-33cf-453a-816b-6d3fdc9322d2

Reported adverse events (FAERS/openFDA)#

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