Oxygen Nitrogen Mixture
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 Nitrogen Mixture
- Generic name
- OXYGEN NITROGEN MIXTURE
- Manufacturer
- General Air Service & Supply Co.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c7f7500c-b521-4d93-a567-898ca4f778f4
- SPL ID
- 44875fd6-d206-f99e-e063-6294a90a4a73
- Version
- 16
- Effective date
- 2025-11-26
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:31:48
| 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 |
|---|---|---|---|
| application applno | NDA | 205849 | derived:openfda.application_number |
| application number | NDA205849 | openfda.application_number | |
| brand name | Oxygen Nitrogen Mixture | openfda.brand_name | |
| generic name | OXYGEN NITROGEN MIXTURE | openfda.generic_name | |
| manufacturer name | General Air Service & Supply Co. | openfda.manufacturer_name | |
| ndc | package | 21220-130-01 | openfda.package_ndc |
| ndc | product | 21220-130 | openfda.product_ndc |
| ndc11 | package | 21220013001 | derived:openfda.package_ndc |
| rxcui | 413101 | openfda.rxcui | |
| spl id | 44875fd6-d206-f99e-e063-6294a90a4a73 | id | |
| spl set id | c7f7500c-b521-4d93-a567-898ca4f778f4 | set_id | |
| unii | S88TT14065 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.