FDA.reportPublic FDA data

Oxygen

Manufacturer
East Coast Oxygen
Effective date
2025-12-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 21:53:22

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

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. Continuous monitoring is required. Uninterrupted use of high concentrations of oxygen over a long duration without monitoring its effect on arterial blood may be harmful. Do not attempt to use on patients who have stopped breathing unless used in conjunction with resuscitative equipment. Keep container refilled with oxygen USP only. Federal law requires this container be refilled with oxygen USP only by establishments registered as a drug manufacturer. Federal law prohibits dispensing without a prescription.

DANGER: MAY CAUSE FIRE OR EXPLOSION IF HEATED. Do not handle until all safety precautions have been read and understood. Keep away from combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or in well-ventilated places. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in piping. Use only with equipment designed for oxygen service. Open valve slowly. Close valve after each use and when empty. 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

OXYGEN

2

EAST COAST OXYGEN

310 Elk Park Drive • Woodfin, NC 28804

(828) 252-7770

NO SMOKING

NO VAPING

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
72808-001-01Oxygen113 L in 1 CYLINDERGAS1138
72808-001-02Oxygen165 L in 1 CYLINDERGAS1658
72808-001-03Oxygen164 L in 1 CYLINDERGAS1648
72808-001-04Oxygen198 L in 1 CYLINDERGAS1988
72808-001-05Oxygen255 L in 1 CYLINDERGAS2558
72808-001-06Oxygen425 L in 1 CYLINDERGAS4258
72808-001-07Oxygen640 L in 1 CYLINDERGAS6408
72808-001-08Oxygen680 L in 1 CYLINDERGAS6808
72808-001-09Oxygen1738 L in 1 CYLINDERGAS17388
72808-001-10Oxygen3455 L in 1 CYLINDERGAS34558
72808-001-11Oxygen7080 L in 1 CYLINDERGAS70808
72808-001-12Oxygen300 L in 1 DEWARGAS3008
72808-001-13Oxygen36 L in 1 DEWARGAS368
72808-001-14Oxygen46 L in 1 DEWARGAS468
72808-001-15Oxygen250 L in 1 DEWARGAS2508

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
72808-00172808-001-01, 72808-001-02, 72808-001-03, 72808-001-04, 72808-001-05, 72808-001-06, 72808-001-07, 72808-001-08, 72808-001-09, 72808-001-10, 72808-001-11, 72808-001-12, 72808-001-13, 72808-001-14, 72808-001-15

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
OxygenOXYGENEast Coast Oxygen84785db1-7298-0a70-e053-2991aa0a260d2025-12-29Exact identifier
ndc (package): 72808-001-13
ndc (package): 72808-001-07
ndc (package): 72808-001-01
ndc (package): 72808-001-03
ndc (package): 72808-001-15
ndc (package): 72808-001-10
ndc (package): 72808-001-14
ndc (package): 72808-001-04
ndc (package): 72808-001-12
ndc (package): 72808-001-05
ndc (package): 72808-001-06
ndc (package): 72808-001-08
ndc (package): 72808-001-09
ndc (package): 72808-001-02
ndc (package): 72808-001-11
ndc (product): 72808-001
ndc11 (package): 72808000114
ndc11 (package): 72808000105
ndc11 (package): 72808000109
ndc11 (package): 72808000101
ndc11 (package): 72808000107
ndc11 (package): 72808000112
ndc11 (package): 72808000108
ndc11 (package): 72808000113
ndc11 (package): 72808000104
ndc11 (package): 72808000102
ndc11 (package): 72808000103
ndc11 (package): 72808000110
ndc11 (package): 72808000106
ndc11 (package): 72808000111
ndc11 (package): 72808000115
spl id: 471bab6a-2886-2e50-e063-6394a90a5c23
spl set id: 84785db1-7298-0a70-e053-2991aa0a260d

Reported adverse events (FAERS/openFDA)#

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