Oxygen

Manufacturer
CBJ Development Co.
Effective date
2025-10-16
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 22:01:44

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 InhalationPSN10
312172oxygen 99 % Gas for InhalationSCD10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72908-001-01Oxygen20 L in 1 DEWARGAS2010
72908-001-02Oxygen719 L in 1 DEWARGAS71910
72908-001-05Oxygen46 L in 1 DEWARGAS4610
72908-001-06Oxygen318 L in 1 DEWARGAS31810
72908-001-07Oxygen1098 L in 1 DEWARGAS109810

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
72908-00172908-001-05, 72908-001-01, 72908-001-06, 72908-001-02, 72908-001-07

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
92025-03-03full-release2026-05-31 21:26:57

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
OxygenOXYGENCBJ Development Co.858e88ca-1833-a4cb-e053-2a91aa0ad4622025-10-16Exact identifier
ndc (package): 72908-001-01
ndc (package): 72908-001-06
ndc (package): 72908-001-07
ndc (package): 72908-001-02
ndc (package): 72908-001-05
ndc (product): 72908-001
ndc11 (package): 72908000107
ndc11 (package): 72908000102
ndc11 (package): 72908000105
ndc11 (package): 72908000106
ndc11 (package): 72908000101
spl id: 414c21ae-b695-4cb7-e063-6294a90a3803
spl set id: 858e88ca-1833-a4cb-e053-2a91aa0ad462

Reported adverse events (FAERS/openFDA)#

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