FDA.reportPublic FDA data

Nitrogen

Manufacturer
Pooch Welding Supply Company, Inc.
Effective date
2010-06-18
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:09:17

Label at a glance#

ProductNitrogen
Active ingredientNitrogen
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 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 temperatures should not exceed 52C (125F). 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 oxygen. 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.
POOCH WELDING SUPPLY 1540 East Empire Ave. Benton Harbor, MI 49022   Phone  (269) 926-1157 Fax (269) 926-1700 E-mail: info@poochwelding.com
43549 (05/05)nitrogennitrogen

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311998nitrogen 99 % Gas for InhalationPSN1
311998nitrogen 99 % Gas for InhalationSCD1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51613-002-012019-10-21C16284748780-1956f9ecf-cdcb-621f-e053-dbdaa90a74adnitrogen
51613-002-022019-10-21C16284748780-1956f9ecf-cdcb-621f-e053-dbdaa90a74adnitrogen
51613-002-032019-10-21C16284748780-1956f9ecf-cdcb-621f-e053-dbdaa90a74adnitrogen
51613-002-042019-10-21C16284748780-1956f9ecf-cdcb-621f-e053-dbdaa90a74adnitrogen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51613-002-01Nitrogen5 L in 1 CYLINDERGAS51
51613-002-02Nitrogen10 L in 1 CYLINDERGAS101
51613-002-03Nitrogen15 L in 1 CYLINDERGAS151
51613-002-04Nitrogen20 L in 1 CYLINDERGAS201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51613-002NITROGEN GAS [POOCH WELDING SUPPLY COMPANY, INC.]1Legacy NDC, 4 package rows20100719_b8561e7c-9d85-44ac-babe-929fb3687e6c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NitrogenACTIVE INGREDIENTN762921K751
NitrogenACTIVE MOIETYN762921K751

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
51613-00251613-002-01, 51613-002-02, 51613-002-03, 51613-002-04

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
cf37de98-8ed6-48d5-81a8-50a5fd861623b8561e7c-9d85-44ac-babe-929fb3687e6c2010-06-18Exact identifier
spl id: cf37de98-8ed6-48d5-81a8-50a5fd861623
spl set id: b8561e7c-9d85-44ac-babe-929fb3687e6c

Reported adverse events (FAERS/openFDA)#

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