Oxygen

Manufacturer
Seeley Enterprises Inc
Effective date
2010-11-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:10:39

Label at a glance#

ProductOxygen
Active ingredientOxygen
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SEELY MEDICAL
OXYGEN, REFRIGERATED LIQUID (CRYOGENIC LIQUID)   UN1073 U.S.P.  Produced by Air Liquefaction
 OXYGEN 2
ALWAYS KEEP CONTAINER IN UPRIGHT POSITION   
WARNING: EXTREMELY COLD, OXIDIZING LIQUID AND GAS UNDER PRESSURE. VIGOROUSLY ACCELERATES COMBUSTION. OXYGEN VIGOROUSLY ACCELERATES COMBUSTION. OXYGEN REACTS VIOLENTLY WITH OIL, GREASE, (BODY OIL, HAND LOTION AND ITEMS CONTAINING OIL OR GREASE) AND CAN CAUSE FIRE AND SEVERE BURNS. COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT. CAN CAUSE SEVERE FROSTBITE.
For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications; Rx Only.
Do not use high concentrations for more than 5 hours without 1 hour interruption.
Keep oil, grease, and combustibles away. Use only with equipment cleaned for oxygen service. Transport, store and use with adequate ventilation in upright position only. Do not get liquid in eyes, on skin, or clothing. For liquid withdrawal, use faceshield and gloves. Use hand truck for container movement. Do not walk or roll equipment over spills. Close valve after each use and when empty. Do not strike arc or laser beam on cylinder. Use in accordance with the Material Safety Data Sheet for this product. Open valve slowly. FIRST AID: IN CASE OF FROSTBITE, obtain medical treatment immediately.
CONTENTS:
Liters     Weight    lbs    oz        Pressure (PSIG @ 70F)
DO NOT REMOVE THIS LABEL.
Manufactured by Seely Medical Andover Ohio 44003-0699
SML040Boxygen labeloxygen label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312175oxygen 99.9 % Gas for InhalationPSN1
312175oxygen 99.9 % Gas for InhalationSCD1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49854-001-012019-10-29C16284748780-1960f7f55-bf96-8e05-e053-dbdaa90a074aOxygen Label
49854-001-022019-10-29C16284748780-1960f7f55-bf96-8e05-e053-dbdaa90a074aOxygen Label
49854-001-032019-10-29C16284748780-1960f7f55-bf96-8e05-e053-dbdaa90a074aOxygen Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49854-001-01Oxygen41 L in 1 CYLINDERGAS411
49854-001-02Oxygen45 L in 1 CYLINDERGAS451
49854-001-03Oxygen450 L in 1 DEWARGAS4501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49854-001OXYGEN GAS [SEELEY ENTERPRISES INC]1Legacy NDC, 3 package rows20101208_3be78b09-9681-45e4-9338-07e5cfed5c55.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OxygenACTIVE INGREDIENTS88TT140651
OxygenACTIVE MOIETYS88TT140651

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
49854-00149854-001-01, 49854-001-02, 49854-001-03

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
0be88133-4808-4bb2-8859-9229ca7f30d53be78b09-9681-45e4-9338-07e5cfed5c552010-11-12Exact identifier
spl id: 0be88133-4808-4bb2-8859-9229ca7f30d5
spl set id: 3be78b09-9681-45e4-9338-07e5cfed5c55

Reported adverse events (FAERS/openFDA)#

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