Air
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
- Air
- Generic name
- BREATHING AIR
- Manufacturer
- Cee-Kay Supply, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 39c4a680-b3ac-478b-8cf9-d0428d3638ad
- SPL ID
- 43d22f54-02b8-00b3-e063-6294a90a3601
- Version
- 19
- Effective date
- 2025-11-17
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:14
| 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 | 207036 | derived:openfda.application_number |
| application number | NDA207036 | openfda.application_number | |
| brand name | Air | openfda.brand_name | |
| generic name | BREATHING AIR | openfda.generic_name | |
| manufacturer name | Cee-Kay Supply, Inc. | openfda.manufacturer_name | |
| ndc | package | 10218-003-04 | openfda.package_ndc |
| ndc | package | 10218-003-01 | openfda.package_ndc |
| ndc | package | 10218-003-07 | openfda.package_ndc |
| ndc | package | 10218-003-06 | openfda.package_ndc |
| ndc | package | 10218-003-02 | openfda.package_ndc |
| ndc | package | 10218-003-05 | openfda.package_ndc |
| ndc | package | 10218-003-03 | openfda.package_ndc |
| ndc | product | 10218-003 | openfda.product_ndc |
| ndc11 | package | 10218000302 | derived:openfda.package_ndc |
| ndc11 | package | 10218000303 | derived:openfda.package_ndc |
| ndc11 | package | 10218000307 | derived:openfda.package_ndc |
| ndc11 | package | 10218000304 | derived:openfda.package_ndc |
| ndc11 | package | 10218000306 | derived:openfda.package_ndc |
| ndc11 | package | 10218000301 | derived:openfda.package_ndc |
| ndc11 | package | 10218000305 | derived:openfda.package_ndc |
| spl id | 43d22f54-02b8-00b3-e063-6294a90a3601 | id | |
| spl set id | 39c4a680-b3ac-478b-8cf9-d0428d3638ad | set_id | |
| unii | K21NZZ5Y0B | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.