Nitrogen
- Manufacturer
- MJB Welding Supply, Inc.
- Effective date
- 2020-03-14
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:39:19
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
MJB Nitrogen, Refrigerated
NITROGEN, REFRIGERATED LIQUID NF UN1977 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
Do not handle until all safety precautions have been read and understood. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, and eye protection. Use a back flow preventive device in the piping. DO NOT change or force fit connections. | NON-FLAMMABLE GAS 2 Close valve after each use and when empty. Always keep container in upright position. Read and follow the Safety Data Sheet (SDS) before use. | |
FIRST AID: | IF INHALED: Remove person to fresh air and keep comfortable for breathing. IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention. CAS: 7727-37-9 | |
MJB 357 EAST PARK AVENUE • P.O. BOX 2166 WELDING SUPLY CHICO, CA 95927 530-342-3589 • FAX 530-342-1715 | ||
SECURE ALL CYLINDERS WHILE IN STORAGE AND IN USE. DO NOT REMOVE THIS PRODUCT LABEL. LABEL SOLUTINS, INC. • 1-800-296-9080 • 86387 (10/18) PN: 86387G-24-28 | ||
Products#
Every source-derived product name is available through these pages.
- Nitrogen
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73705-002 | 73705-002-01, 73705-002-02 |
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 |
|---|---|---|---|---|---|---|
| 9360ded5-d21a-48a3-938a-2563fa3ad891 | 17214a82-c65f-477d-90ed-ca899c6259bc | 2022-01-13 | 17214a82-c65f-477d-90ed-ca899c6259bc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
