Oxygen

Manufacturer
AdaptHealth Minnesota LLC
Effective date
2021-11-15
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:27:50

Label at a glance#

ProductOxygen
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Oxygen Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LOX LabelLOX Label

Oxygen, Compressed

USP UN1072

Produced by Air Liquefaction

Danger: May cause or intensify fire;oxidizer. Contains gas under pressure;may explode if heated.
C.A.S. 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.

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.

Lot StickerLot Sticker

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
81610-00181610-001-01, 81610-001-02, 81610-001-03, 81610-001-04

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
e9d68939-61bc-7b85-e053-2a95a90af64ebbf2f00b-fb92-7f3b-e053-2995a90a4e8b2022-09-29Exact identifier
spl set id: bbf2f00b-fb92-7f3b-e053-2995a90a4e8b

Reported adverse events (FAERS/openFDA)#

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