Oxygen
- Manufacturer
- WELDERS SUPPLY COMPANY OF LOUISVILLE, INC.
- Effective date
- 2026-04-28
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 5
- Source
- full-release
- Hydrated at
- 2026-05-31 22:17:05
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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 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.
DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. Obtain, read and follow the safety instructions before use. Keep away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Use and store only outdoors or with adequate ventilation. Store 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 equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. Do not open valve until connected to equipment prepared for use. 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. CAS: 7782-44-7 DO NOT REMOVE THIS PRODUCT LABEL.
WELDERS SUPPLY & GASES
331 Boxley Avenue Louisville, KY 40209
502-637-4771
NO SMOKING
NO VAPING
CONTENTS:
LTRS:
CU.FT.
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84078-002-01 | Oxygen | 8510 L in 1 CYLINDER | GAS | 8510 | 5 | |
| 84078-002-02 | Oxygen | 150 L in 1 CYLINDER | GAS | 150 | 5 | |
| 84078-002-03 | Oxygen | 120 L in 1 CYLINDER | GAS | 120 | 5 | |
| 84078-002-04 | Oxygen | 425 L in 1 CYLINDER | GAS | 425 | 5 | |
| 84078-002-05 | Oxygen | 705 L in 1 CYLINDER | GAS | 705 | 5 | |
| 84078-002-06 | Oxygen | 532 L in 1 CYLINDER | GAS | 532 | 5 | |
| 84078-002-07 | Oxygen | 3324 L in 1 CYLINDER | GAS | 3324 | 5 | |
| 84078-002-08 | Oxygen | 6414 L in 1 CYLINDER | GAS | 6414 | 5 | |
| 84078-002-09 | Oxygen | 137100 L in 1 CYLINDER | GAS | 137100 | 5 | |
| 84078-002-10 | Oxygen | 180 L in 1 CYLINDER | GAS | 180 | 5 |
Products#
Every source-derived product name is available through these pages.
- Oxygen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84078-002 | 84078-002-01, 84078-002-02, 84078-002-03, 84078-002-04, 84078-002-05, 84078-002-06, 84078-002-07, 84078-002-08, 84078-002-09, 84078-002-10 |
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 |
|---|---|---|---|
| 4 | 2026-01-28 | monthly-update | 2026-06-03 17:55:44 |
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 | WELDERS SUPPLY COMPANY OF LOUISVILLE, INC. | 1017fba9-0472-88cf-e063-6294a90afe1c | 2026-04-28 | 84078-002-06 84078-002-01 84078-002-05 84078-002-10 84078-002-07 84078-002-04 84078-002-02 84078-002-08 84078-002-03 84078-002-09 84078-002 84078000210 84078000209 84078000205 84078000206 84078000201 84078000207 84078000203 84078000204 84078000208 84078000202 508742c3-256a-48a7-e063-6394a90acf3e 1017fba9-0472-88cf-e063-6294a90afe1c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
