Oxygen
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
- Generic name
- OXYGEN
- Manufacturer
- Heckman Healthcare Service & Supplies Inc. dba Quipt Home Medical
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c7d32bbc-4493-48ef-b935-96cc60689a41
- SPL ID
- 4691b73c-12a4-0e07-e063-6394a90a37c3
- Version
- 22
- Effective date
- 2025-12-22
- Source export date
- 2026-10-30
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:26:38
| 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 | openfda.brand_name | |
| generic name | OXYGEN | openfda.generic_name | |
| manufacturer name | Heckman Healthcare Service & Supplies Inc. dba Quipt Home Medical | openfda.manufacturer_name | |
| ndc | package | 53835-001-06 | openfda.package_ndc |
| ndc | package | 53835-001-03 | openfda.package_ndc |
| ndc | package | 53835-001-05 | openfda.package_ndc |
| ndc | package | 53835-001-08 | openfda.package_ndc |
| ndc | package | 53835-001-01 | openfda.package_ndc |
| ndc | package | 53835-001-09 | openfda.package_ndc |
| ndc | package | 53835-001-02 | openfda.package_ndc |
| ndc | package | 53835-001-11 | openfda.package_ndc |
| ndc | package | 53835-001-07 | openfda.package_ndc |
| ndc | package | 53835-001-10 | openfda.package_ndc |
| ndc | package | 53835-001-04 | openfda.package_ndc |
| ndc | product | 53835-001 | openfda.product_ndc |
| ndc11 | package | 53835000101 | derived:openfda.package_ndc |
| ndc11 | package | 53835000103 | derived:openfda.package_ndc |
| ndc11 | package | 53835000104 | derived:openfda.package_ndc |
| ndc11 | package | 53835000102 | derived:openfda.package_ndc |
| ndc11 | package | 53835000111 | derived:openfda.package_ndc |
| ndc11 | package | 53835000106 | derived:openfda.package_ndc |
| ndc11 | package | 53835000105 | derived:openfda.package_ndc |
| ndc11 | package | 53835000108 | derived:openfda.package_ndc |
| ndc11 | package | 53835000109 | derived:openfda.package_ndc |
| ndc11 | package | 53835000110 | derived:openfda.package_ndc |
| ndc11 | package | 53835000107 | derived:openfda.package_ndc |
| rxcui | 312172 | openfda.rxcui | |
| spl id | 4691b73c-12a4-0e07-e063-6394a90a37c3 | id | |
| spl set id | c7d32bbc-4493-48ef-b935-96cc60689a41 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.