Oxygen

Manufacturer
Eureka Oxygen Company
Effective date
2025-10-07
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
12
Source
full-release
Hydrated at
2026-05-31 22:00:15

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure3 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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. Keep out of reach of children. Federal law requires that this container be refilled with oxygen USP only by establishments registered as a drug manufacturer in accordance with the Federal Food, Drug, and Cosmetic Act.

DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED.

Do not handle until all safety precautions have been read and understood. Keep 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. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Safety Data Sheet (SDS) before use.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

NO SMOKING

NO VAPING

EUREKA OXYGEN COMPANY

2810 JACOBS AVE. EUREKA, CA 95501

(707) 443-2228 oxygen one 2025oxygen one 2025

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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. Keep out of reach of children. Federal law required that this container be refilled with oxygen USP only by establishments registered as a drug manufacturer in accordance with the Federal Food, Drug and Cosmetic Act. DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Do not handle until all safety precautions have been read and understood. Keep 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. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. Protect from sunlight when ambient temperature exceeds 52 C (125 F). Read and follow the Safety Data Sheet (SDS) before use.

CAS 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.

NO SMOKING

NO VAPING

EUREKA OXYGEN COMPANY

2810 JACOBS AVE. EUREKA, CA 95501

(707) 443-2228 oxygen two 2025oxygen two 2025

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRIGERATED LIQUID

OXYGEN, REFRIGERATED LIQUID USP

UN1073

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. Keep out of reach of children. Federal law requires that this container be refilled with oxygen USP only by establishments registered as a drug manufacturer in accordance with the Federal Food, Drug, and Cosmetic Act.

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 LIQUIDS MAY EXPLODE ON IGNITION OR IMPACT.

Do not handle until all safety precautions have been read and understood. Keep 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 and either face shield or eye protection. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. Always keep container in upright position. DO NOT change or force fit connections. Avoid spills. Do not walk on or roll equipment over spills. 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.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL

NO SMOKING

NO VAPING

EUREKA OXYGEN COMPANY

2810 JACOBS AVE. EUREKA, CA 95501

(707) 443-2228 refrigerated oxygen 2025refrigerated oxygen 2025

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN12
312172oxygen 99 % Gas for InhalationSCD12

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66754-001-01Oxygen595 L in 1 CYLINDERGAS59512
66754-001-02Oxygen1302 L in 1 CYLINDERGAS130212
66754-001-03Oxygen2378 L in 1 CYLINDERGAS237812
66754-001-04Oxygen3540 L in 1 CYLINDERGAS354012
66754-001-05Oxygen7107 L in 1 CYLINDERGAS710712
66754-001-06Oxygen9543 L in 1 CYLINDERGAS954312
66754-001-07Oxygen180 L in 1 DEWARGAS18012

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
66754-00166754-001-01, 66754-001-02, 66754-001-03, 66754-001-04, 66754-001-05, 66754-001-06, 66754-001-07

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
112024-10-28full-release2026-05-31 21:15:50

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

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
OxygenOXYGENEureka Oxygen Company0b776546-e469-41cd-b9d6-d9f6b9e698902025-10-07Exact identifier
ndc (package): 66754-001-07
ndc (package): 66754-001-05
ndc (package): 66754-001-01
ndc (package): 66754-001-03
ndc (package): 66754-001-02
ndc (package): 66754-001-04
ndc (package): 66754-001-06
ndc (product): 66754-001
ndc11 (package): 66754000104
ndc11 (package): 66754000101
ndc11 (package): 66754000103
ndc11 (package): 66754000106
ndc11 (package): 66754000102
ndc11 (package): 66754000107
ndc11 (package): 66754000105
spl id: 40950add-d52f-50fc-e063-6394a90a2423
spl set id: 0b776546-e469-41cd-b9d6-d9f6b9e69890

Reported adverse events (FAERS/openFDA)#

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