Oxygen
- Manufacturer
- Carepro Health Risk Management | Care Pro
- Effective date
- 2025-10-30
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 13
- Source
- full-release
- Hydrated at
- 2026-05-31 22:03:28
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
OXYGEN, COMPRESSED USP
UN 1072
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. Use only with equipment of compatible materials of construction and rated for cylinder pressure. 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 52 C (125 F). Read and follow the Safety Data Sheet (SDS) before use.
DO NOT REMOVE THIS PRODUCT LABEL.
WARNING: No smoking or vaping. For emergency use only when administered by properly trained personnel for oxygen deficiency and resuscitation. For all other medical applications, Rx Required. 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.
Produced by Air Liquefaction.
NO SMOKING
NO VAPING
CAS NO: 7782-44-7
Contents / Sizes:
113 Liters M4
165 Liters M6
255 Liters C
425 Liters D
680 Liters E
7080 Liters H
Liters Other
CarePro Home Medical
971 33rd Ave SW
Cedar Rapids, IA 52404
319-298-0953
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42389-001-01 | Oxygen | 113 L in 1 CYLINDER | GAS | 113 | 13 | |
| 42389-001-02 | Oxygen | 170 L in 1 CYLINDER | GAS | 170 | 13 | |
| 42389-001-03 | Oxygen | 248 L in 1 CYLINDER | GAS | 248 | 13 | |
| 42389-001-04 | Oxygen | 415 L in 1 CYLINDER | GAS | 415 | 13 | |
| 42389-001-05 | Oxygen | 682 L in 1 CYLINDER | GAS | 682 | 13 | |
| 42389-001-06 | Oxygen | 1724 L in 1 CYLINDER | GAS | 1724 | 13 | |
| 42389-001-07 | Oxygen | 3452 L in 1 CYLINDER | GAS | 3452 | 13 | |
| 42389-001-08 | Oxygen | 6910 L in 1 CYLINDER | GAS | 6910 | 13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| OXYGEN | ACTIVE INGREDIENT | S88TT14065 | 3 | |
| Oxygen | ACTIVE MOIETY | S88TT14065 | 3 |
Products#
Every source-derived product name is available through these pages.
- Oxygen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 42389-001 | 42389-001-01, 42389-001-02, 42389-001-03, 42389-001-04, 42389-001-05, 42389-001-06, 42389-001-07, 42389-001-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| OXYGEN | S88TT14065 | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 12 | 2024-10-21 | full-release | 2026-05-31 21:15:14 |
| 11 | 2023-10-06 | full-release | 2026-05-31 20:53:46 |
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 |
|---|---|---|---|---|---|---|
| Oxygen | OXYGEN | Carepro Health Risk Management | 79b3a2f5-db50-4c48-a5c9-3e4ccc92ae9e | 2025-10-30 | 42389-001-03 42389-001-01 42389-001-04 42389-001-05 42389-001-08 42389-001-06 42389-001-07 42389-001-02 42389-001 42389000105 42389000101 42389000108 42389000106 42389000103 42389000107 42389000102 42389000104 426653f5-af9b-b791-e063-6294a90ab914 79b3a2f5-db50-4c48-a5c9-3e4ccc92ae9e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
