Oxygen

Manufacturer
Laramie Respiratory Service
Effective date
2020-12-16
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 20:34:10

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RepresentativeHPLabelRepresentativeHPLabel

OXYGEN

COMPRESSED

USP

UN 1072

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 NO: 7782-44-7

DO NOT REMOVE THIS PRODUCT LABEL.

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. Produced by Air Liquefaction.

RepresentativeLotStickerRepresentativeLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN4
312172oxygen 99 % Gas for InhalationSCD4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50101-0001-22022-01-28C16284748780-1d6a99b3a-009e-a426-e053-dadaa90af4c2Oxygen
50101-0001-32022-01-28C16284748780-1d6a99b3a-009e-a426-e053-dadaa90af4c2Oxygen
50101-0001-42022-01-28C16284748780-1d6a99b3a-009e-a426-e053-dadaa90af4c2Oxygen
50101-0001-52022-01-28C16284748780-1d6a99b3a-009e-a426-e053-dadaa90af4c2Oxygen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50101-0001-2Oxygen248 L in 1 CYLINDERGAS2484
50101-0001-3Oxygen415 L in 1 CYLINDERGAS4154
50101-0001-4Oxygen682 L in 1 CYLINDERGAS6824
50101-0001-5Oxygen164 L in 1 CYLINDERGAS1644

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50101-0001OXYGEN GAS [LARAMIE RESPIRATORY SERVICE]4Legacy NDC, 4 package rows20201217_7907c8e9-cfc7-4297-bf9d-1c7eb298d46a.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
50101-000150101-0001-5, 50101-0001-2, 50101-0001-3, 50101-0001-4

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
b696d280-4857-2259-e053-2a95a90a60617907c8e9-cfc7-4297-bf9d-1c7eb298d46a2020-12-16Exact identifier
spl id: b696d280-4857-2259-e053-2a95a90a6061
spl set id: 7907c8e9-cfc7-4297-bf9d-1c7eb298d46a

Reported adverse events (FAERS/openFDA)#

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