FDA.reportPublic FDA data

Nitrogen

Manufacturer
Linde Gas & Equipment Inc.
Effective date
2021-12-14
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
16
Source
legacy-cache
Hydrated at
2026-08-01 22:20:59

Label at a glance#

ProductNitrogen
Active ingredientNitrogen
Label structure2 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION


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 REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. 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. 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. 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.

             

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N2 Liquid Label
N2 Liquid Label

Linde

NITROGEN, REFRIGERATED LIQUID

NF

UN1977
CAS 7727-37-9

Produced by Air Liquefaction

2

MEDICAL GAS
Rx only.

WARNING: USE OF ADAPTORS PROHIBITED

WARNING: DO NOT REMOVE FITTINGS

DO NOT REMOVE THIS LABEL

WARNING: USE OF ADAPTORS IS PROHIBITED

WARNING: DO NOT REMOVE FITTINGS

CONTENTS:
CYLINDER TYPELITERS
160L[_]97244
180L[_]105055
200L[_]115209
230L[_]133955
__________________

Distributed by:
Linde Gas North America LLC
200 Somerset Corporate Blvd., Suite 7000
Bridgewater, NJ 08807
866.543.3427

LG021F

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
25373-102-072025-12-18C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-082025-12-18C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-092025-12-18C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-102025-12-18C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-072022-07-29C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-082022-07-29C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-092022-07-29C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID
25373-102-102022-07-29C16284748780-1e4f33bdf-a887-d8a0-e053-dadaa90a6e4eNITROGEN, REFRIGERATED LIQUID

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25373-102NITROGEN (NITROGEN) GAS [LINDE GAS & EQUIPMENT INC.]16Legacy NDC20211225_8b74d539-adab-536b-bdda-a943498ef783.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NitrogenACTIVE INGREDIENTN762921K757
NitrogenACTIVE MOIETYN762921K757

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
25373-10225373-102-07, 25373-102-08, 25373-102-09, 25373-102-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
NitrogenN762921K75ACTIB

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
cabe2208-7694-4c32-8334-f5e34cd402788b74d539-adab-536b-bdda-a943498ef7832025-12-18WarningsExact identifier
spl set id: 8b74d539-adab-536b-bdda-a943498ef783

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.