OXYGEN

Manufacturer
Gilmore Liquid Air Co.
Effective date
2024-10-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 21:15:09

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure2 sections

Label contents#

Full prescribing information#

OXYGEN COMPRESSED LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OXYGEN, COMPRESSED USP UN 1072 OXYGEN 2 GLA-31

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.  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.

GILMORE LIQUID AIR COMPANY

South El Monte, CA 91733

626-443-1361

HP LABELHP LABEL

OXYGEN REFRIGERATED LIQUID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Oxygen, Refrigerated Liquid, USP UN1073

Rx ONLY

Rx ONLY. 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. 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

GILMORE

LIQUID AIR COMPANY

South El Monte, CA 91733

626-443-1361

GLA-8

E15

LIQUID LABELLIQUID LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN10
312172oxygen 99 % Gas for InhalationSCD10

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51012-001-01OXYGEN170 L in 1 CYLINDERGAS17010
51012-001-02OXYGEN248 L in 1 CYLINDERGAS24810
51012-001-03OXYGEN426 L in 1 CYLINDERGAS42610
51012-001-04OXYGEN671 L in 1 CYLINDERGAS67110
51012-001-05OXYGEN3462 L in 1 CYLINDERGAS346210
51012-001-06OXYGEN6482 L in 1 CYLINDERGAS648210
51012-001-07OXYGEN7900 L in 1 CYLINDERGAS790010
51012-001-08OXYGEN9600 L in 1 CYLINDERGAS960010
51012-001-09OXYGEN145360 L in 1 DEWARGAS14536010
51012-001-10OXYGEN156700 L in 1 DEWARGAS15670010
51012-001-11OXYGEN387367 L in 1 TANKGAS38736710

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51012-001OXYGEN GAS [GILMORE LIQUID AIR CO.]10Current NDC, Legacy NDC, 11 package rows20241023_03fbd6e5-09a6-4f13-b251-63cf9ff129e9.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#

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
OXYGENOXYGENGilmore Liquid Air Co.03fbd6e5-09a6-4f13-b251-63cf9ff129e92024-10-21Exact identifier
ndc (package): 51012-001-01
ndc (package): 51012-001-03
ndc (package): 51012-001-05
ndc (package): 51012-001-10
ndc (package): 51012-001-08
ndc (package): 51012-001-02
ndc (package): 51012-001-09
ndc (package): 51012-001-04
ndc (package): 51012-001-06
ndc (package): 51012-001-07
ndc (package): 51012-001-11
ndc (product): 51012-001
ndc11 (package): 51012000110
ndc11 (package): 51012000101
ndc11 (package): 51012000105
ndc11 (package): 51012000108
ndc11 (package): 51012000111
ndc11 (package): 51012000107
ndc11 (package): 51012000102
ndc11 (package): 51012000109
ndc11 (package): 51012000106
ndc11 (package): 51012000103
ndc11 (package): 51012000104
spl id: 6af2649a-d5b6-4aee-99fe-2b252da914d8
spl set id: 03fbd6e5-09a6-4f13-b251-63cf9ff129e9

Reported adverse events (FAERS/openFDA)#

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