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#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
OXYGEN, 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 | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70423-001-09 | 2024-12-20 | C162847 | 48780-1 | 9d75b9d0-b698-f424-e053-dadaa90a57ce | 2c5e9c23-12ab-3ddb-e054-00144ff88e88 |
| 70423-001-09 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b698-f424-e053-dadaa90a57ce | 2c5e9c23-12ab-3ddb-e054-00144ff88e88 |
Products#
Every source-derived product name is available through these pages.
- OXYGEN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 70423-001 | 70423-001-09 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| OXYGEN | S88TT14065 | ACTIB |
Source Document#
Orange Book application contexts#
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 29bcae2e-e86c-1652-e063-6394a90a4218 | 2c5e9c23-12ab-3ddb-e054-00144ff88e88 | 2024-12-20 | 2c5e9c23-12ab-3ddb-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
