Oxygen Refrigerated Liquid
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Oxygen Refrigerated Liquid
- Generic name
- OXYGEN REFRIGERATED LIQUID
- Manufacturer
- Dallas Life Support Systems Inc
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 277714d5-6d6a-70d4-e054-00144ff88e88
- SPL ID
- 407f089f-d21e-cc42-e063-6294a90a756a
- Version
- 12
- Effective date
- 2025-10-06
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:16:51
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Oxygen Compressed Gas | openfda.brand_name | |
| brand name | Oxygen Refrigerated Liquid | openfda.brand_name | |
| generic name | OXYGEN COMPRESSED GAS | openfda.generic_name | |
| generic name | OXYGEN REFRIGERATED LIQUID | openfda.generic_name | |
| manufacturer name | Dallas Life Support Systems Inc | openfda.manufacturer_name | |
| ndc | package | 62145-001-14 | openfda.package_ndc |
| ndc | package | 62145-001-08 | openfda.package_ndc |
| ndc | package | 62145-002-02 | openfda.package_ndc |
| ndc | package | 62145-001-04 | openfda.package_ndc |
| ndc | package | 62145-001-02 | openfda.package_ndc |
| ndc | package | 62145-001-03 | openfda.package_ndc |
| ndc | package | 62145-001-07 | openfda.package_ndc |
| ndc | package | 62145-001-13 | openfda.package_ndc |
| ndc | package | 62145-002-01 | openfda.package_ndc |
| ndc | package | 62145-001-11 | openfda.package_ndc |
| ndc | package | 62145-001-12 | openfda.package_ndc |
| ndc | package | 62145-001-06 | openfda.package_ndc |
| ndc | package | 62145-001-09 | openfda.package_ndc |
| ndc | package | 62145-001-01 | openfda.package_ndc |
| ndc | package | 62145-001-10 | openfda.package_ndc |
| ndc | package | 62145-002-03 | openfda.package_ndc |
| ndc | package | 62145-001-05 | openfda.package_ndc |
| ndc | product | 62145-001 | openfda.product_ndc |
| ndc | product | 62145-002 | openfda.product_ndc |
| ndc11 | package | 62145000112 | derived:openfda.package_ndc |
| ndc11 | package | 62145000106 | derived:openfda.package_ndc |
| ndc11 | package | 62145000101 | derived:openfda.package_ndc |
| ndc11 | package | 62145000109 | derived:openfda.package_ndc |
| ndc11 | package | 62145000105 | derived:openfda.package_ndc |
| ndc11 | package | 62145000108 | derived:openfda.package_ndc |
| ndc11 | package | 62145000201 | derived:openfda.package_ndc |
| ndc11 | package | 62145000102 | derived:openfda.package_ndc |
| ndc11 | package | 62145000113 | derived:openfda.package_ndc |
| ndc11 | package | 62145000103 | derived:openfda.package_ndc |
| ndc11 | package | 62145000104 | derived:openfda.package_ndc |
| ndc11 | package | 62145000203 | derived:openfda.package_ndc |
| ndc11 | package | 62145000110 | derived:openfda.package_ndc |
| ndc11 | package | 62145000114 | derived:openfda.package_ndc |
| ndc11 | package | 62145000107 | derived:openfda.package_ndc |
| ndc11 | package | 62145000202 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.