OXYGEN

Manufacturer
Sexton Weldilng Supply Co., Inc.
Effective date
2018-12-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:36:40

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure3 sections

Label contents#

Full prescribing information#

OXYGEN COMPRESSED LABEL

WARNINGS AND PRECAUTIONS SECTION

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. USE ONLY WITH PRESSURE REDUCING EQUIPMENT AND APPARATUS DESIGNED FOR OXYGEN. DON NOT ATTEMPT TO USE ON PATIENTS WHO HAVE STOPPED BREATHING UNLESS USED IN CONJUNCTION WITH RESUSCITATIVE EQUIPMENT.

WARNING: HIGH PRESSURE OXIDIZING GAS. VIGOROUSLY ACCELERATED COMBUSTION. KEEP OIL AND GREASE AWAY. OPEN VALVE SLOWLY. STORE AND USE WITH ADEQUATE VENTILATION. USE ONLY WITH EQUIPMENT CLEANED FOR OXYGEN SERVICE AND RATED FOR CYLINDER PRESSURE. CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. CYLINDER TEMPERATURE SHOULD NOT EXCEED 52 C (125 F). USE IN ACCORDANCE WITH MATERIAL SAFETY DATA SHEET

DO NOT REMOVE THIS PRODUCT LABEL.

OXYGEN COMPRESSED LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN COMPRESSED USP UN 1072 OXYGEN-2

FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION.  FEDERAL LAW REQUIRES THAT THIS CONTAINER BE REFILLED WITH OXYGEN USP ONLY BY ESTABLISHMENTS REGISTERED AS A DRUG PRODUCER IN ACCORDANCE WITH THE FEDERAL FOOD DRUG AND COSMETIC ACT.  PRODUCED BY AIR LIQUEFACTION.

CAUTION: USE NO OIL ON VALVE OR CONNECTIONS.  TRANSFILLING OF THIS PRODUCT IS PROHIBITED  CAS 7782-44-7

SIZE      CONTENTS

E            682 LITERS

D            415 LITERS

C            248 LITERS  

A            113 LITERS     

M6         165 LITERS

H               6900   LITERS

B            170 LITERS

OTHER   ______________ LITERS

SHOULDER LABELSHOULDER LABEL

BODY LABELBODY LABEL

res

OXYGEN REFRIGERATED LIQUID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN REFRIGERATED LIQUID USP UN 1073 Rx ONLY OXYGEN-2

ALWAYS KEEP CONTAINER IN UPRIGHT POSITION.  EXTREMELY COLD LIQUID AND GAS UNDER PRESSURE.  VIGOROUSLY ACCELERATES COMBUSTION.  COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT.    CAN CAUSE SEVERE FROSTBITE.  DO NOT GET LIQUID IN EYES, ON SKIN OR CLOTHING.  FOR LIQUID WITHDRAWAL WEAR FACE SHIELD AND GLOVES.  DO NOT DROP OR HANDLE CONTAINER ROUGHLY.  USE SUITABLE HAND TRUCK FOR CONTAINER MOVEMENT.  AVOID SPILLS  DO NOT WALK OR ROLL EQUIPMENT OVER SPILLS.  CONTAINER TEMPERATURE SHOULD NOT EXCEED 52 C (125 F)

FIRST AID  IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY.

PRODUCED BY AIR LIQUEFACTION.  CAUTION: USE NO OIL ON VALVE OR CONNECTIONS.  TRANSFILLING OF THIS LIQUID OR GAS IS PROHIBITED.

LIQUID LABELLIQUID LABEL

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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#

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
db9bb5e7-81f3-60d2-e053-2a95a90a5cc14d15710c-3474-4580-893d-3d7f89c4a4ec2022-03-29WarningsExact identifier
spl set id: 4d15710c-3474-4580-893d-3d7f89c4a4ec

Reported adverse events (FAERS/openFDA)#

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