oxygen
- Manufacturer
- Austin Respiratory Equipment,inc
- Effective date
- 2017-11-13
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 10
- Source
- full-release
- Hydrated at
- 2026-05-31 20:24:49
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
OXYGEN,
REFRIGERATED LIQUID
USP
UN: 1073
CAS NO:7782-44-7
_________________________________________________________________
WARNING
EXTREMELY COLD, OXIDIZING LIQUID AND GAS UNDER PRESSURE.
VIGOROUSLY ACCELERATES COMBUSTION. COMBUSTIBLES IN
CONTACT WITYH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR
IMPACT. CAN CAUSE SEVERE FROSTBITE.
For emergency use only when administered by properly trained personnel for
Oxygen deficiency and resuscitation. For all other medical applications Rx only
Federal law prohibits dispensing without a prescription. WARNING: 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. Federal law requires that this Container be Refilled with oxygen U.S.P.
only by Establishments Registered as Drug Producer in accordance with the Federal
Food, Drug and Cosmetic Act.
KEEP OUT OF REACH OF CHILDERN.
DO NOT REMOVE THIS PRODUCT LABEL.
Produced by Air Liquefaction.
Directions for use:↑Always keep container in upright position↑. Do not change or force fit connections. Keep oil, grease, and combustibles away. No smoking in cylinder area. use only with equipment cleaned for oxygen service. Store and use with adequate ventilation. Do not get liquid in eyes, on skin, or on clothing. For liquid withdrawal, wear face shield and gloves. Do not drop. Use suitable hand truck for container movement.
Avoid spills. Do not walk or roll equipment over spills. Cylinder temperature should not exceed 52°C (125°F).Close valve after each use and when empty. Use a back flow preventive device in the piping. Use in accordance with Safety data Sheet. (SDS).
FIRST AID: in case of Frostbite: obtain medical treatment immediately.
SIZE CONTENT
21 16,750 LITERS
31 24,950 LITERS
41 33,500 LITERS
AUSTIN RESPIRATORY EQUIPMENT, INC.
1676 N. Belcher Road
Clearwater, FL. 33765
(727) 467-0606
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64540-011-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-41d4-f424-e053-dadaa90a57ce | 4a9ffc3c-3e47-4fa8-b201-c4233ccc109e |
| 64540-011-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-41d4-f424-e053-dadaa90a57ce | 4a9ffc3c-3e47-4fa8-b201-c4233ccc109e |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64540-011-01 | oxygen | 21 L in 1 DEWAR | GAS | 21 | 10 | |
| 64540-011-02 | oxygen | 41 L in 1 DEWAR | GAS | 41 | 10 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| OXYGEN | ACTIVE INGREDIENT | S88TT14065 | 9 | |
| OXYGEN | ACTIVE MOIETY | S88TT14065 | 9 |
Products#
Every source-derived product name is available through these pages.
- oxygen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 64540-011 | 64540-011-01, 64540-011-02 |
| 11390-001 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| OXYGEN | S88TT14065 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 206f040f-3e08-4ffa-9e88-288fd112fb8a | 4a9ffc3c-3e47-4fa8-b201-c4233ccc109e | 2017-11-13 | 206f040f-3e08-4ffa-9e88-288fd112fb8a 4a9ffc3c-3e47-4fa8-b201-c4233ccc109e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
