FDA.reportPublic FDA data

OXYGEN

Manufacturer
Ohio Valley Acquisition Corp dba Ohio Valley Medical Gas & Supply, Inc. | Ohio Valley Medical Gas & Supply, Inc.
Effective date
2022-11-04
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 20:44:48

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

OXYGEN REFRIGERATED LIQUID USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRIGERATED LIQUID

OXYGEN, REFRIGERATED LIQUID USP UN1073

OXYGEN 2

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 of 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; OXIDER, CONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. COMBUSTIBELS 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 the equipment of compatible materials 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 FIRST AID: IF ON SKIN: Thaw affected parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.

CAS: 7782-44-7 

DO NOT REMOVE THIS PRODUCT LABEL

OHIO VALLEY MEDICAL GAS & SUPPLY

1415 NORTH ROYAL AVE.

EVANSVILLE, IN 47715 • 812-423-3617

LIQUID LABELLIQUID LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN7
312172oxygen 99 % Gas for InhalationSCD7

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75892-001-012024-01-30C16284748780-11030e365-30c5-111a-e063-dadaa90a10e2b7f09350-2b95-4cab-8ac1-effbf4339c45
75892-001-022024-01-30C16284748780-11030e365-30c5-111a-e063-dadaa90a10e2b7f09350-2b95-4cab-8ac1-effbf4339c45
75892-001-032024-01-30C16284748780-11030e365-30c5-111a-e063-dadaa90a10e2b7f09350-2b95-4cab-8ac1-effbf4339c45
75892-001-042024-01-30C16284748780-11030e365-30c5-111a-e063-dadaa90a10e2b7f09350-2b95-4cab-8ac1-effbf4339c45
75892-001-052024-01-30C16284748780-11030e365-30c5-111a-e063-dadaa90a10e2b7f09350-2b95-4cab-8ac1-effbf4339c45

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75892-001-01OXYGEN21 L in 1 DEWARGAS217
75892-001-02OXYGEN31 L in 1 DEWARGAS317
75892-001-03OXYGEN35 L in 1 DEWARGAS357
75892-001-04OXYGEN40 L in 1 DEWARGAS407
75892-001-05OXYGEN45 L in 1 DEWARGAS457

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75892-001OXYGEN GAS [OHIO VALLEY ACQUISITION CORP DBA OHIO VALLEY MEDICAL GAS & SUPPLY, INC.]7Legacy NDC, 5 package rows20221105_b7f09350-2b95-4cab-8ac1-effbf4339c45.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
75892-00175892-001-01, 75892-001-02, 75892-001-03, 75892-001-04, 75892-001-05

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

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
6abddf99-ab1d-4287-bd30-6dacb318581db7f09350-2b95-4cab-8ac1-effbf4339c452022-11-04Exact identifier
spl id: 6abddf99-ab1d-4287-bd30-6dacb318581d
spl set id: b7f09350-2b95-4cab-8ac1-effbf4339c45

Reported adverse events (FAERS/openFDA)#

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