NITROGEN
- Manufacturer
- Capitol Welders Supply Co., Inc.
- Effective date
- 2018-10-18
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:48:46
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
Nitrogen Liquid Label
REFRIGERATED LIQUID
NITROGEN, REFRIGERATED LIQUID NF UN1977 NON-FLAMMABLE GAS 2
↑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 52°C (125°F). 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.
Filled and Distributed by:
Capitol Welders Supply Co.
5111 Choctaw Drive • Baton Rouge, LA
(225) 383-3717
43549
(05/05)
NITROGEN COMPRESSED NF product label
NITROGEN COMPRESSED NF
UN 1066
NON-FLAMMABLE GAS 2
37049 (01/15)
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: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Use a back flow preventive device in the piping. Use only with equipment rated for cylinder pressure. Close valve after each use and when empty. Protect from sunlight when ambient tempersture exceeds 52°C (125°F). Read and follow the Safety Data Sheet (SDS) before use. FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Get medical advice/attention. CAS: 7727-37-9 DO NOT REMOVE THIS PRODUCT LABEL.
CW FILLED AND DISTRIBUTED BY: CAPITOL WELDERS SUPPLY CO.
5111 CHOCTAW DRIVE • BATON ROUGE, LA 70805
CONTENTS: LTRS:
_________________ CU FT:
FDA-Initiated Inactive NDC Indexing#
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
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 49571-002 | 49571-002-01, 49571-002-02, 49571-002-03, 49571-002-04, 49571-002-05, 49571-002-06, 49571-002-07, 49571-002-08, 49571-002-09, 49571-002-10, 49571-002-11 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NITROGEN | N762921K75 | 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 |
|---|---|---|---|---|---|---|
| 1929a4d3-ef1a-4217-9039-1acb4c9bc6e4 | cc078b00-3cbe-4fe2-aef4-ee73b75628bf | 2025-12-08 | cc078b00-3cbe-4fe2-aef4-ee73b75628bf |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

