Nitrogen
- Manufacturer
- Gases Plus Norco, LLC | Gases Plus Norco, LLC-Casper | Gases Plus Norco, LLC-Gillette | Gases Plus Norco, LLC-Billings | Gases Plus Norco, LLC-Rock Springs | Gases Plus Norco, LLC-Cheyenne
- Effective date
- 2009-09-24
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 20:09:25
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ALWAYS KEEP CONTAINER IN UPRIGHT POSITION. DO NOT CHANGE OR FORCE FIT CONNECTIONS.
Rx only.
WARNING: Administration of Nitrogen may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of Nitrogen and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications, and side effects and the precautions to be taken.
WARNING: EXTREMELY COLD LIQUID AND GAS UNDER PRESSURE. CAN CAUSE RAPID SUFFOCATION. CAN CAUSE SEVERE FROSTBITE.
Store and use with adequate ventilation. Do not get liquid in eyes, on skin or clothing. For liquid withdrawal, wear face shield and gloves. Do not drop. Use suitable hand truck for container movement. Cylinder temperature should not exceed 52oC (125oF). Close valve after each use and when empty. Use a back flow preventive device in the piping. Use in accordance with the Material Safety Data Sheet (MSDS).
FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician.
IN CASE OF FROSTBITE, obtain medical treatment immediately. CAS: 7727-37-9
DO NOT REMOVE THIS PRODUCT LABEL.
GASES PLUS NORCOGILLETTE, WY 82718
(307) 682-8250
45349 (05/05)
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51758-003-01 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-cebe-621f-e053-dbdaa90a74ad | REFRIGERATED LIQUID NITROGEN, REFRIGERATED LIQUID NF UN1977 |
| 51758-003-02 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-cebe-621f-e053-dbdaa90a74ad | REFRIGERATED LIQUID NITROGEN, REFRIGERATED LIQUID NF UN1977 |
| 51758-003-03 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-cebe-621f-e053-dbdaa90a74ad | REFRIGERATED LIQUID NITROGEN, REFRIGERATED LIQUID NF UN1977 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51758-003-01 | Nitrogenc70f6047-a0cb-4f70-aa3a-78acd681efc3 | 165 L in 1 DEWAR | LIQUID | 165 | 1 | |
| 51758-003-02 | Nitrogenc70f6047-a0cb-4f70-aa3a-78acd681efc3 | 185 L in 1 DEWAR | LIQUID | 185 | 1 | |
| 51758-003-03 | Nitrogenc70f6047-a0cb-4f70-aa3a-78acd681efc3 | 196 L in 1 DEWAR | LIQUID | 196 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Nitrogen | ACTIVE INGREDIENT | N762921K75 | 1 | |
| Nitrogen | ACTIVE MOIETY | N762921K75 | 1 |
Products#
Every source-derived product name is available through these pages.
- Nitrogen c70f6047-a0cb-4f70-aa3a-78acd681efc3
- Nitrogen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 51758-003 | 51758-003-01, 51758-003-02, 51758-003-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Nitrogen | N762921K75 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| c4aa9587-bddb-4243-b765-c4d17966e6d4 | ff470a26-ec81-4c15-acfc-fd3aa5426194 | 2009-09-24 | c4aa9587-bddb-4243-b765-c4d17966e6d4 ff470a26-ec81-4c15-acfc-fd3aa5426194 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
