OXYGEN

Manufacturer
Oxygen Service Company, Inc | OXYGEN SERVICE CO., INC. | OXYGEN SERVICE COMPANY
Effective date
2024-11-11
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
12
Source
legacy-cache
Hydrated at
2026-08-01 20:49:35

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure2 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 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. 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 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. 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. 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 SERVICE CO.

1111 PIERCE BUTLER RTE . SAINT PAUL, MN 55104 . (651) 644-7273

1002 INDUSTRIAL DRIVE . SAUK RAPIDS, MN 56379 . (320) 252-5494

CONTENTS: LTRS

CU. FT. oxygen hpoxygen hp

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 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. 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 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.

CAS: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL

OXYGEN SERVICE CO.

1111 PIERCE BUTLER RTE . SAINT PAUL, MN 55104 . (651) 644-7273

1002 INDUSTRIAL DRIVE . SAUK RAPIDS, MN 56379 . (320) 252-5494 oxygen liquidoxygen liquid

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49696-622OXYGEN GAS [OXYGEN SERVICE COMPANY, INC]12Legacy NDC20241114_46d58bb3-7072-4994-9312-e1345e14b354.zip
49696-632OXYGEN GAS [OXYGEN SERVICE COMPANY, INC]12Legacy NDC20241114_46d58bb3-7072-4994-9312-e1345e14b354.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#

Product NDC, Package NDC table
Product NDCPackage NDC
49696-62249696-622-01, 49696-622-02, 49696-622-03, 49696-622-04
49696-63249696-632-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
OXYGENS88TT14065ACTIB
OXYGENS88TT14065ACTIB

Source Document#

Source XML · Source PDF

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
4ee16eae-1aae-148f-e063-6294a90a0dd646d58bb3-7072-4994-9312-e1345e14b3542026-04-07Exact identifier
spl set id: 46d58bb3-7072-4994-9312-e1345e14b354

Reported adverse events (FAERS/openFDA)#

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