Oxygen

Manufacturer
Ogles Oxygen, LLC
Effective date
2023-12-27
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:16:46

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HP LabelHP Label

Oxygen, Compressed

USP UN1072

Produced by Air Liquefaction

Do Not Remove

This Product Label.

Danger: May cause or intensify fire; oxidizer.

Contains gas under pressure; may explode if heated.

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. Keep out of reach of children. Federal law

requires that this container by refilled with oxygen USP only by established registered as a drug

manufacturer in accordance with the federal Food, Drug and Cosmetic Act.

Danger: 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 cleaned

for oxygen service. Open valve slowly. Close valve after each use and when empty. Protect from

sunlight when ambient temperature exceeds 52ºC(125ºF) Read and follow the Safety Data Sheet

(SDS) before use.

RepresentativeLotStickerRepresentativeLotSticker

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74911-00174911-001-01, 74911-001-02, 74911-001-03, 74911-001-04

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
2206b950-c5c4-fe37-e063-6394a90a3415a2df9855-12ac-018c-e053-2a95a90a4b7c2024-09-13Exact identifier
spl set id: a2df9855-12ac-018c-e053-2a95a90a4b7c

Reported adverse events (FAERS/openFDA)#

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