OXYGEN

Manufacturer
DANI Inc
Effective date
2016-02-22
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:28:13

Label at a glance#

ProductOXYGEN
Active ingredientOXYGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Size C9Size C9OXYGEN, COMPRESSED USP UN 1072

DANGER:

COMPRESSED. OXIDIZING GAS. MAY CAUSE OR INTENSIFY FIRE: OXIDIZER. CONTAINS GAS UNDER PRESSURE: MAY EXPLODE IF HEATED.

In case of fire: stop leak if safe to do so. Keep reduction valves free from grease and oil. Open valve slowly. Store and use in a well ventilated place. Use a back flow preventative device in the piping. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52 "C/125 °F. Container temperature should not exceed 52 °C/125°F. Do not handle until all safety precautions have been read and understood. Keep/store away from combustible materials. Use only with equipment cleaned for oxygen service and rated for cylinder pressure.

DO NOT REMOVE THIS PRODUCT LABEL.

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. Use only with

pressure reducing equipment and apparatus designed

for oxygen. Do not attempt to use on patients who have

stopped breathing unless used in conjunction with resuscitative

equipment. Produced by Air Liquefaction. CAS NO: 7782-44-7

SIZE MC 9SCF/255 Liters

DANI Inc

58 Walker Lane

Newtown, PA 18940-1888 USA

TEL: 1-800-423-1100 FAX: 1-888-4231102

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70423-001-092024-12-20C16284748780-19d75b9d0-b698-f424-e053-dadaa90a57ce2c5e9c23-12ab-3ddb-e054-00144ff88e88
70423-001-092020-01-31C16284748780-19d75b9d0-b698-f424-e053-dadaa90a57ce2c5e9c23-12ab-3ddb-e054-00144ff88e88

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
70423-00170423-001-09

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

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
29bcae2e-e86c-1652-e063-6394a90a42182c5e9c23-12ab-3ddb-e054-00144ff88e882024-12-20Exact identifier
spl set id: 2c5e9c23-12ab-3ddb-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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