NITROGEN

Manufacturer
Specialty Gases of America LLC
Effective date
2011-11-03
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:13:11

Label at a glance#

ProductNITROGEN
Active ingredientNITROGEN
Label structure1 sections

Label contents#

Full prescribing information#

NITROGEN REFRIGERATED LIQUID NF LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRIGERATED LIQUID  NITROGEN REFRIGERATED LIQUID NF  NON-FLAMMABLE GAS-2 UN1977  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 GET ABOVE 52 C (125 F)  CLOSE VALVE AFTER EACH USE AND WHEN EMPTY.  USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING.  USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS)

FIRST AID: IN INHALED, REMOVE TO FRESH AIR.  IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION.  IF BREATHING DIFFICULT, GIVE OXYGEN.  CALL A PHYSICIAN.  IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY.

CAS: 7727-37-9  DO NOT REMOVE THIS PRODUCT LABEL.

LIQUID LABELLIQUID LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311998nitrogen 99 % Gas for InhalationPSN2
311998nitrogen 99 % Gas for InhalationSCD2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59754-002-01NITROGEN180 L in 1 DEWARGAS1802
59754-002-02NITROGEN185 L in 1 DEWARGAS1852
59754-002-03NITROGEN230 L in 1 DEWARGAS2302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59754-002NITROGEN GAS [SPECIALTY GASES OF AMERICA LLC]2Legacy NDC, 3 package rows20111104_a95178b6-7faf-4ffd-9137-91f77d388b46.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROGENACTIVE INGREDIENTN762921K752
NITROGENACTIVE MOIETYN762921K752

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
59754-00259754-002-01, 59754-002-02, 59754-002-03

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
3c2687c5-ce06-4322-8977-eccd3fea3ff4a95178b6-7faf-4ffd-9137-91f77d388b462011-11-03Exact identifier
spl id: 3c2687c5-ce06-4322-8977-eccd3fea3ff4
spl set id: a95178b6-7faf-4ffd-9137-91f77d388b46

Reported adverse events (FAERS/openFDA)#

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