oxygen

Manufacturer
Fox Welding Supply Inc
Effective date
2011-05-09
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 20:11:53

Label at a glance#

Productoxygen
Active ingredientoxygen
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN REFRIGERATED LIQUID, USP UN 1073
(CRYOGENIC LIQUID) Produced by Air Liquefaction
ALWAYS KEP CONTAINER IN UPRIGHT POSITION.
WARNING
WARNING: EXTREMELY COLD OXIDIZING LIQDUI AND GAS UNDER PRESSURE. VIGOROUSLY ACCELERATED COMBUSTION. COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT. CAN CAUSE SEVERE FROSTBITE.

For emergency use only when administered b properly trained personnel for xogyen deficiency and resuscitation. For all other medical applications, RX only.

WARNING: Uninterrupted use of high concentrations of oxygen over long diruation, without monitoring its effects on oxygen content in arerial blood, may be harmful. Use only with pressure reducing equipment, and apparatus designed for oxygen. Do not attempt to use on patients who have stopped breathing, unless used in conjunction with resuscitative equipment. Keep oil, grease and combustibles away. Use only with equipment cleaned for oxygen service. Store and use with adequate ventilation. Do not get liquid in eyes, on skin or clothing. For liquid withdrawal, wear face shield and gloves. Do not drop. Use hand truck for container movement. Avoid spills. Do not walk on or roll equipment over spills. Close valve after each use and when empty. Use in accordance with Material Safety Data Sheet.
DO NOT REMOVE THIS PRODUCT LABEL.
FIRST AID
IN CASE OF FROSTBITE, obtain medical treatment immediately.
PLEASE REFER TO THE MATERIAL SAFETY DATA SHEET FOR SAFETY AND PRODUCT INFORMATION
Company Name:
Lot Number:
Contents:
Expiration Date:

WARNING: Caution Federal Law Prohibits Dispensing without Prescription.Oxygen Label 1Oxygen Label 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN3
312172oxygen 99 % Gas for InhalationSCD3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50975-001-01oxygen99 L in 1 CYLINDERGAS993
50975-001-02oxygen141 L in 1 CYLINDERGAS1413
50975-001-03oxygen234 L in 1 CYLINDERGAS2343
50975-001-04oxygen387 L in 1 CYLINDERGAS3873
50975-001-05oxygen643 L in 1 CYLINDERGAS6433
50975-001-06oxygen2540 L in 1 CYLINDERGAS25403
50975-001-07oxygen7100 L in 1 CYLINDERGAS71003
50975-001-08oxygen9401 L in 1 CYLINDERGAS94013
50975-001-09oxygen181850 L in 1 DEWARGAS1818503
50975-001-10oxygen125783 L in 1 DEWARGAS1257833
50975-001-11oxygen129379 L in 1 DEWARGAS1293793
50975-001-12oxygen35962 L in 1 DEWARGAS359623

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50975-001OXYGEN GAS [FOX WELDING SUPPLY INC]3Legacy NDC, 12 package rows20110509_f9749a4b-4bac-48c8-ae3e-31030cbff260.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
oxygenACTIVE INGREDIENTS88TT140653
oxygenACTIVE MOIETYS88TT140653

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

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
53930432-8f66-4865-8a8f-59d997cfaa01f9749a4b-4bac-48c8-ae3e-31030cbff2602011-05-09Exact identifier
spl id: 53930432-8f66-4865-8a8f-59d997cfaa01
spl set id: f9749a4b-4bac-48c8-ae3e-31030cbff260

Reported adverse events (FAERS/openFDA)#

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