FDA.reportPublic FDA data

Oxygen

Manufacturer
Tennessee Medical Equipment, Inc.
Effective date
2025-12-09
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 21:49:43

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HPLabelHPLabel

PRODUCED BY AIR LIQUEFICATION

OXYGEN

COMPRESSED

USP

UN 1072

DO NOT REMOVE THIS PRODUCT LABEL
DANGER
COMPRESSED, OXYDIZING GAS
MAY CAUSE OR INTENSIFY FIRE,
OXIDIZER CONTAINS GAS UNDER

PRESSURE: MAY EXPLODE IF HEATED
Filled and Distributed by:
Tennessee Medical Equipment Inc
4637 Hwy 19 E

Ripley, TN 38063
(731) 635-2119

WARNING: HIGH PRESSURE, OXIDIZING GAS, VIGUROUSLY ACCELERATES COMBUSTION.

Do not handle until all safety precautions have been read and understood.
Keep and store away from clothing and other combustible materials.

NO SMOKING IN THE PRESENCE OF OXYGEN OR FIRE MAY RESULT.
Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation.
Use only with equipment cleaned for oxygen service and rated for cylinder pressure.
Use a back flow preventative device in piping. Close valve after each use and when empty. Cylinder temperature should not exceed 52 C or 125 F.
Use in accordance with Materials Safety Data Sheet (MSDS).

WARNING: No Vaping
For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, RX Required.
Uninterrupted use of high concentrations of oxygen over long durations 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 in conjunction with resuscitative equipment.

RepresentativeLOXLabelRepresentativeLOXLabel

OXYGEN,

REFRIGERATED

LIQUID USP

UN 1073

CONTENTS ________________LITERS

CAS NO: 7782-44-7

DANGER:

MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS

REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS
OR INJURY. COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT.

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. Wear cold insulating gloves, face

shield, and eye protection. In case of fire: Stop leak if safe to do so. Use a

back flow preventive device in the piping. Use only with equipment of

compatible materials of construction and rated for cylinder pressure. Use

only with equipment cleaned for oxygen service. DO NOT change or force

fit connections. Avoid spills. Do not walk on or roll equipment over spills.

Close valve after each use and when empty. Always keep container in

upright position. 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 advice/attention.

DO NOT REMOVE THIS PRODUCT LABEL.

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. Do not attempt to use on patients who have

stopped breathing unless used in conjunction with resuscitative equipment.

Produced by Air Liquefaction. RepresentativeLotStickerRepresentativeLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN8
312172oxygen 99 % Gas for InhalationSCD8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73008-001-01Oxygen113 L in 1 CYLINDERGAS1138
73008-001-02Oxygen165 L in 1 CYLINDERGAS1658
73008-001-03Oxygen164 L in 1 CYLINDERGAS1648
73008-001-04Oxygen198 L in 1 CYLINDERGAS1988
73008-001-05Oxygen255 L in 1 CYLINDERGAS2558
73008-001-06Oxygen425 L in 1 CYLINDERGAS4258
73008-001-07Oxygen640 L in 1 CYLINDERGAS6408
73008-001-08Oxygen680 L in 1 CYLINDERGAS6808
73008-001-09Oxygen1738 L in 1 CYLINDERGAS17388
73008-001-10Oxygen3455 L in 1 CYLINDERGAS34558
73008-001-11Oxygen7080 L in 1 CYLINDERGAS70808
73008-001-12Oxygen21 L in 1 DEWARGAS218
73008-001-13Oxygen30 L in 1 DEWARGAS308
73008-001-14Oxygen35 L in 1 DEWARGAS358
73008-001-15Oxygen36 L in 1 DEWARGAS368
73008-001-16Oxygen41 L in 1 DEWARGAS418
73008-001-17Oxygen45 L in 1 DEWARGAS458
73008-001-18Oxygen46 L in 1 DEWARGAS468

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
73008-00173008-001-03, 73008-001-02, 73008-001-01, 73008-001-04, 73008-001-05, 73008-001-06, 73008-001-07, 73008-001-08, 73008-001-09, 73008-001-10, 73008-001-11, 73008-001-12, 73008-001-13, 73008-001-14, 73008-001-15, 73008-001-16, 73008-001-17, 73008-001-18

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
OxygenOXYGENTennessee Medical Equipment, Inc.84f1c5b0-2d76-394f-e053-2a91aa0aaf1f2025-12-09Exact identifier
ndc (package): 73008-001-03
ndc (package): 73008-001-01
ndc (package): 73008-001-14
ndc (package): 73008-001-18
ndc (package): 73008-001-08
ndc (package): 73008-001-13
ndc (package): 73008-001-09
ndc (package): 73008-001-04
ndc (package): 73008-001-05
ndc (package): 73008-001-16
ndc (package): 73008-001-12
ndc (package): 73008-001-15
ndc (package): 73008-001-17
ndc (package): 73008-001-07
ndc (package): 73008-001-02
ndc (package): 73008-001-10
ndc (package): 73008-001-06
ndc (package): 73008-001-11
ndc (product): 73008-001
ndc11 (package): 73008000105
ndc11 (package): 73008000109
ndc11 (package): 73008000108
ndc11 (package): 73008000101
ndc11 (package): 73008000117
ndc11 (package): 73008000107
ndc11 (package): 73008000113
ndc11 (package): 73008000110
ndc11 (package): 73008000102
ndc11 (package): 73008000114
ndc11 (package): 73008000116
ndc11 (package): 73008000111
ndc11 (package): 73008000115
ndc11 (package): 73008000106
ndc11 (package): 73008000118
ndc11 (package): 73008000112
ndc11 (package): 73008000103
ndc11 (package): 73008000104
spl id: 458b81a7-35b6-8024-e063-6394a90afeac
spl set id: 84f1c5b0-2d76-394f-e053-2a91aa0aaf1f

Reported adverse events (FAERS/openFDA)#

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