Oxygen

Manufacturer
Vantage DME Partnership dba Vantage Home Medical Equipment and Services
Effective date
2025-10-07
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-05-31 22:01:05

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HPLabelHPLabel

OXYGEN, COMPRESSED USP
UN1072

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

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 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. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. 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.

Produced by Air Liquefaction

NO SMOKING – NO VAPING

LOXLabelLOXLabel

UN1073
OXYGEN, REFRIGERATED LIQUID USP

For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, ℞ required.

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 OXIDIZING REFRIGERATED LIQUIDS MAY EXPLODE ON IGNITION OR IMPACT.

Do not handle until all safety precautions have been read and understood. Keep 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 and either face shield or eye protection. In case of fire: Stop leak if safe to do so. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. Always keep container in upright position. DO NOT change or force fit connections. Avoid spills. Do not walk on or roll equipment over spills. 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
WARNING: REFIRGERATED LIQUID
OXYGEN USP

DO NOT REMOVE THIS PRODUCT LABEL
NO SMOKING – NO VAPING

RepresentativeLotStickerRepresentativeLotSticker

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312172oxygen 99 % Gas for InhalationPSN14
312172oxygen 99 % Gas for InhalationSCD14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62671-001-01Oxygen113 L in 1 CYLINDERGAS11314
62671-001-02Oxygen425 L in 1 CYLINDERGAS42514
62671-001-03Oxygen680 L in 1 CYLINDERGAS68014
62671-001-04Oxygen3455 L in 1 CYLINDERGAS345514
62671-001-07Oxygen41 L in 1 DEWARGAS4114
62671-001-08Oxygen46 L in 1 DEWARGAS4614
62671-001-09Oxygen7080 L in 1 CYLINDERGAS708014

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
62671-00162671-001-01, 62671-001-02, 62671-001-03, 62671-001-04, 62671-001-07, 62671-001-08, 62671-001-09

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
132024-12-26full-release2026-05-31 21:20:41

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
OxygenOXYGENVantage DME Partnership dba Vantage Home Medical Equipment and Services84752e57-4311-119f-e053-2991aa0ab8132025-10-07Exact identifier
ndc (package): 62671-001-01
ndc (package): 62671-001-09
ndc (package): 62671-001-07
ndc (package): 62671-001-02
ndc (package): 62671-001-03
ndc (package): 62671-001-08
ndc (package): 62671-001-04
ndc (product): 62671-001
ndc11 (package): 62671000107
ndc11 (package): 62671000109
ndc11 (package): 62671000104
ndc11 (package): 62671000102
ndc11 (package): 62671000103
ndc11 (package): 62671000101
ndc11 (package): 62671000108
spl id: 4096294b-7876-1cca-e063-6294a90a2208
spl set id: 84752e57-4311-119f-e053-2991aa0ab813

Reported adverse events (FAERS/openFDA)#

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