Oxygen

Manufacturer
GC Medical Equipment, Inc.
Effective date
2025-10-06
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:00:23

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HPLabelHPLabel

OXYGEN, COMPRESSED USP

UN1072

PRODUCED BY AIR LIQUEFACTION

WARNING:

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 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.

DANGER:

MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Obtain, read and follow all safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use only with equipment cleaned for oxygen service and rated for cylinder pressure. Use only with equipment of compatible materials of construction. Open valve slowly. Close valve after each use and when empty. Store and use with adequate ventilation. Protect from sunlight and physical damage. Always keep container in upright position. Use a backflow preventive device in the piping. Read and follow the Safety Data Sheet (SDS) before use.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

GC Medical Equipment Co., Inc.
4651 State Road
Peninsula, OH 44264
888-338-0202

NO SMOKING — NO VAPING

CompressedLotStickerCompressedLotSticker

LOXLabelLOXLabel

REFRIGERATED LIQUID

OXYGEN, REFRIGERATED LIQUID USP

UN1073

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

CONTENTS: _______ LTRS: _______ CU.FT.: _______

WARNING:

For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For other medical applications, RX required.

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.

DANGER:

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

Obtain, read and follow all safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use only outdoors or in well-ventilated area. Store and transport in upright position. Wear cold insulating gloves/face shield/eye protection. In case of fire: Stop leak if safe to do so. Use a backflow preventive device in the piping. Use only with equipment of compatible materials of construction and suitable for cryogenic service. 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 hoses. 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 help.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

GC Medical Equipment Co., Inc.
4651 State Road
Peninsula, OH 44264
888-338-0202

NO SMOKING — NO VAPING

LOXLotStickerLOXLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
348017oxygen 99.1 % Gas for InhalationPSN5
348017oxygen 99.1 % Gas for InhalationSCD5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66878-001-01Oxygen113 L in 1 CYLINDERGAS1135
66878-001-02Oxygen164 L in 1 CYLINDERGAS1645
66878-001-03Oxygen170 L in 1 CYLINDERGAS1705
66878-001-04Oxygen248 L in 1 CYLINDERGAS2485
66878-001-05Oxygen425 L in 1 CYLINDERGAS4255
66878-001-06Oxygen566 L in 1 CYLINDERGAS5665
66878-001-07Oxygen596 L in 1 CYLINDERGAS5965
66878-001-08Oxygen616 L in 1 CYLINDERGAS6165
66878-001-09Oxygen675 L in 1 CYLINDERGAS6755
66878-001-10Oxygen1699 L in 1 CYLINDERGAS16995
66878-001-11Oxygen3450 L in 1 CYLINDERGAS34505
66878-001-12Oxygen7106 L in 1 CYLINDERGAS71065
66878-001-13Oxygen9544 L in 1 CYLINDERGAS95445
66878-001-14Oxygen28 L in 1 DEWARGAS285
66878-001-15Oxygen40 L in 1 DEWARGAS405
66878-001-16Oxygen55 L in 1 DEWARGAS555
66878-001-18Oxygen180 L in 1 DEWARGAS1805
66878-001-19Oxygen41 L in 1 DEWARGAS415
66878-001-20Oxygen45 L in 1 DEWARGAS455

Products#

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

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

NDC Codes#

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-03full-release2026-05-31 21:13:33

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
OxygenOXYGENGC Medical Equipment, Inc.d9e30b98-ec71-f132-e053-2995a90af69f2025-10-06Exact identifier
ndc (package): 66878-001-10
ndc (package): 66878-001-02
ndc (package): 66878-001-06
ndc (package): 66878-001-07
ndc (package): 66878-001-08
ndc (package): 66878-001-14
ndc (package): 66878-001-15
ndc (package): 66878-001-01
ndc (package): 66878-001-19
ndc (package): 66878-001-11
ndc (package): 66878-001-16
ndc (package): 66878-001-03
ndc (package): 66878-001-13
ndc (package): 66878-001-20
ndc (package): 66878-001-04
ndc (package): 66878-001-12
ndc (package): 66878-001-18
ndc (package): 66878-001-05
ndc (package): 66878-001-09
ndc (product): 66878-001
ndc11 (package): 66878000119
ndc11 (package): 66878000106
ndc11 (package): 66878000120
ndc11 (package): 66878000109
ndc11 (package): 66878000110
ndc11 (package): 66878000112
ndc11 (package): 66878000104
ndc11 (package): 66878000107
ndc11 (package): 66878000108
ndc11 (package): 66878000116
ndc11 (package): 66878000114
ndc11 (package): 66878000102
ndc11 (package): 66878000118
ndc11 (package): 66878000111
ndc11 (package): 66878000115
ndc11 (package): 66878000103
ndc11 (package): 66878000101
ndc11 (package): 66878000105
ndc11 (package): 66878000113
spl id: 4083a8cf-1584-815a-e063-6394a90a2015
spl set id: d9e30b98-ec71-f132-e053-2995a90af69f

Reported adverse events (FAERS/openFDA)#

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