FDA.reportPublic FDA data

OXYGEN

Manufacturer
Enos Home Oxygen Therapy, Inc.
Effective date
2025-11-25
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 21:47:15

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure3 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

WARNING: For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications Rx only.

DO NOT REMOVE THIS LABEL

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OXYGEN COMPRESSED LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN COMPRESSED U.S.P.  UN 1072 Oxygen produced by air liquefaction Warning: Oxidizing gas which vigorously accelerates combustion. Handle and store with care. Do not drop. Keep upright. Do not use or store near heat or flame. Keep free from oil or grease. Use only with equipment designed, cleaned and rated for use with medical oxygen systems. Open valve slowly. Close valve after each use and when empty. Uninterrupted use of high concentrations of oxygen over an extended period of time without monitoring its effects may be harmful. Do not attempt to use on patients who have stopped breathing, unless used in conjunction with resuscitative equipment.

Filled by: ENOS HOME OXYGEN AND MEDICAL SUPPLY, INC.
35 Welby Road New Bedford, MA 02745
508-992-2146 1-800-473-4669

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OXYGEN REFRIGERATED LIQUID LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN REFRIGERATED LIQUID U.S.P. UN 1073Oxygen produced by air liquefaction Warning: Oxidizing gas which vigorously accelerates combustion. Handle and store with care. Do not drop. Keep upright. Do not use or store near heat or flame. Keep free from oil or grease. Use only with equipment designed, cleaned and rated for use with medical oxygen systems. Open valve slowly. Close valve after each use and when empty. Uninterrupted use of high concentrations of oxygen over an extended period of time without monitoring its effects may be harmful. Do not attempt to use on patients who have stopped breathing, unless used in conjunction with resuscitative equipment.

Filled by: ENOS HOME OXYGEN AND MEDICAL SUPPLY, INC.
35 Welby Road New Bedford, MA 02745
508-992-2146 1-800-473-4669


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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312173oxygen 99.5 % Gas for InhalationPSN8
312173oxygen 99.5 % Gas for InhalationSCD8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58987-001-01OXYGEN113 L in 1 CYLINDERGAS1138
58987-001-02OXYGEN165 L in 1 CYLINDERGAS1658
58987-001-03OXYGEN240 L in 1 CYLINDERGAS2408
58987-001-04OXYGEN415 L in 1 CYLINDERGAS4158
58987-001-05OXYGEN682 L in 1 CYLINDERGAS6828
58987-001-06OXYGEN3450 L in 1 CYLINDERGAS34508

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
58987-00158987-001-01, 58987-001-02, 58987-001-03, 58987-001-04, 58987-001-05, 58987-001-06

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 · Source PDF

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
OXYGENOXYGENEnos Home Oxygen Therapy, Inc.97d49ca6-3d70-4a84-8a8b-38a8bc3463c52025-11-25WarningsExact identifier
ndc (package): 58987-001-06
ndc (package): 58987-001-03
ndc (package): 58987-001-05
ndc (package): 58987-001-04
ndc (package): 58987-001-01
ndc (package): 58987-001-02
ndc (product): 58987-001
ndc11 (package): 58987000101
ndc11 (package): 58987000103
ndc11 (package): 58987000106
ndc11 (package): 58987000104
ndc11 (package): 58987000102
ndc11 (package): 58987000105
spl id: ca4dc987-1173-450c-a8fb-f0be5727c27a
spl set id: 97d49ca6-3d70-4a84-8a8b-38a8bc3463c5

Reported adverse events (FAERS/openFDA)#

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