Oxygen
- Manufacturer
- Medox Corporation
- Effective date
- 2025-12-30
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 17
- Source
- full-release
- Hydrated at
- 2026-05-31 21:53:17
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
Principal for Oxygen Product
MEDOX CORPORATION
OXYGEN, COMPRESSED
USP
UN1072
PRODUCED BY AIR LIQUEFACTION
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 be refilled with oxygen USP only by establishments registered as a drug manufacturer in accordance with the Federal Food, Drug, and Cosmetic Act.
DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER.
CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED.
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.
Close valve after each use and when empty.
Use only with equipment rated for cylinder pressure.
Do not open valve until connected to equipment prepared for use.
Use only equipment of compatible materials of construction.
Open valve slowly.
Use only with equipment cleaned for oxygen service.
Protect from sunlight when ambient temperature exceeds 52°C (125°F).
Read and follow the Safety Data Sheet (SDS) before use.
OXYGEN
2
DO NOT REMOVE
THIS PRODUCT LABEL
4233 CLARK RD #20
SARASOTA, FL 34233 • 941-923-3461
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53683-0001-1 | Oxygen | 180 L in 1 CYLINDER | GAS | 180 | 17 | |
| 53683-0001-2 | Oxygen | 240 L in 1 CYLINDER | GAS | 240 | 17 | |
| 53683-0001-3 | Oxygen | 415 L in 1 CYLINDER | GAS | 415 | 17 | |
| 53683-0001-4 | Oxygen | 682 L in 1 CYLINDER | GAS | 682 | 17 | |
| 53683-0001-5 | Oxygen | 640 L in 1 CYLINDER | GAS | 640 | 17 | |
| 53683-0001-6 | Oxygen | 1738 L in 1 CYLINDER | GAS | 1738 | 17 | |
| 53683-0001-7 | Oxygen | 3455 L in 1 CYLINDER | GAS | 3455 | 17 | |
| 53683-0001-8 | Oxygen | 7080 L in 1 CYLINDER | GAS | 7080 | 17 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Oxygen | ACTIVE INGREDIENT | S88TT14065 | 1 | |
| Oxygen | ACTIVE MOIETY | S88TT14065 | 1 |
Products#
Every source-derived product name is available through these pages.
- Oxygen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53683-0001 | 53683-0001-1, 53683-0001-2, 53683-0001-3, 53683-0001-4, 53683-0001-5, 53683-0001-6, 53683-0001-7, 53683-0001-8 |
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 |
|---|---|---|---|---|---|---|
| Oxygen | OXYGEN | Medox Corporation | 5baca5cc-47a4-4a01-bf1f-7ebc5e225326 | 2025-12-30 | 53683-0001-4 53683-0001-6 53683-0001-1 53683-0001-3 53683-0001-8 53683-0001-7 53683-0001-5 53683-0001-2 53683-0001 53683000107 53683000101 53683000104 53683000105 53683000102 53683000103 53683000106 53683000108 47317ad1-0379-c236-e063-6394a90ab118 5baca5cc-47a4-4a01-bf1f-7ebc5e225326 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

