Oxygen
- Manufacturer
- Linde Puerto Rico B.V.
- Effective date
- 2025-12-31
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 20
- Source
- full-release
- Hydrated at
- 2026-05-31 21:53:35
Label at a glance#
ProductNitrogen
Active ingredientNITROGEN, OXYGEN
Label structure2 sections
Label contents#
Full prescribing information#
Proof of Delivery Oxygen USP
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11324-499-01 | Nitrogen | 25000 L in 1 TANK | GAS | 25000 | 20 | |
| 11324-721-02 | Oxygen | 18000 L in 1 TANK | GAS | 18000 | 20 | |
| 11324-721-03 | Oxygen | 10000 L in 1 TANK | GAS | 10000 | 20 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| NITROGEN | ACTIVE INGREDIENT | N762921K75 | 2 | |
| OXYGEN | ACTIVE INGREDIENT | S88TT14065 | 2 | |
| NITROGEN | ACTIVE MOIETY | N762921K75 | 2 | |
| OXYGEN | ACTIVE MOIETY | S88TT14065 | 2 |
Products#
Every source-derived product name is available through these pages.
- Nitrogen
- Oxygen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11324-721 | 11324-721-02, 11324-721-03 |
| 11324-499 | 11324-499-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NITROGEN | N762921K75 | ACTIB |
| OXYGEN | S88TT14065 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| Nitrogen | NITROGEN | Linde Puerto Rico B.V. | 4e5df6ce-06ef-498f-b064-b2b6e1521951 | 2025-12-31 | 11324-499-01 11324-721-02 11324-721-03 11324-721 11324-499 11324049901 11324072103 11324072102 474215c3-14e6-3d25-e063-6394a90aa80a 4e5df6ce-06ef-498f-b064-b2b6e1521951 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

