FDA.reportPublic FDA data

Nitrogen

Manufacturer
Minneapolis Oxygen Company
Effective date
2025-12-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-05-31 21:47:47

Label at a glance#

ProductNitrogen
Active ingredientNITROGEN
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROGEN, COMPRESSED NF UN1066 NON-FLAMMABLE GAS 2 NITROGEN NF
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 temperature exceeds 52 degrees C (125 degrees 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. CONTENTS: LTRS. CU. FT.
MINNEAPOLIS OXYGEN COMPANY 3842 WASHINGTON AVENUE, N . MINNEAPOLIS, MN 55412
612-588-8855 nitrogen onenitrogen one

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRIGERATED LIQUID NITROGEN, REFRIGERATED LIQUID NF UN1977
NON-FLAMMABLE GAS 2
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 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.
CAS: 7727-37-9 CONTENTS: LTRS: CU FT: DO NOT REMOVE THIS PRODUCT LABEL
MINNEAPOLIS OXYGEN COMPANY 3842 WASHINGTON AVENUE, N . MINNEAPOLIS, MN 55412
612-588-8855 nitrogen twonitrogen two

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311998nitrogen 99 % Gas for InhalationPSN16
311998nitrogen 99 % Gas for InhalationSCD16

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55147-002-01Nitrogen391 L in 1 CYLINDERGAS39116
55147-002-02Nitrogen651 L in 1 CYLINDERGAS65116
55147-002-03Nitrogen3257 L in 1 CYLINDERGAS325716
55147-002-04Nitrogen7222 L in 1 CYLINDERGAS722216
55147-002-05Nitrogen8420 L in 1 CYLINDERGAS842016
55147-002-06Nitrogen4247 L in 1 CYLINDERGAS424716
55147-002-07Nitrogen10 L in 1 DEWARGAS1016
55147-002-08Nitrogen195 L in 1 DEWARGAS19516
55147-002-09Nitrogen3030 L in 1 CYLINDERGAS303016
55147-002-10Nitrogen5863 L in 1 CYLINDERGAS586316
55147-002-11Nitrogen7801 L in 1 CYLINDERGAS780116
55147-002-12Nitrogen20 L in 1 DEWARGAS2016

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
55147-00255147-002-01, 55147-002-02, 55147-002-03, 55147-002-04, 55147-002-05, 55147-002-06, 55147-002-07, 55147-002-08, 55147-002-09, 55147-002-10, 55147-002-11, 55147-002-12

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

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

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
NitrogenNITROGENMinneapolis Oxygen Companyc3fdbc5c-da70-4cbd-bdee-eddb4d852b262025-12-01Exact identifier
ndc (package): 55147-002-02
ndc (package): 55147-002-06
ndc (package): 55147-002-09
ndc (package): 55147-002-08
ndc (package): 55147-002-04
ndc (package): 55147-002-01
ndc (package): 55147-002-03
ndc (package): 55147-002-11
ndc (package): 55147-002-12
ndc (package): 55147-002-05
ndc (package): 55147-002-10
ndc (package): 55147-002-07
ndc (product): 55147-002
ndc11 (package): 55147000204
ndc11 (package): 55147000201
ndc11 (package): 55147000206
ndc11 (package): 55147000211
ndc11 (package): 55147000209
ndc11 (package): 55147000208
ndc11 (package): 55147000210
ndc11 (package): 55147000205
ndc11 (package): 55147000212
ndc11 (package): 55147000203
ndc11 (package): 55147000202
ndc11 (package): 55147000207
spl id: 44eb832f-4438-0da1-e063-6394a90ae833
spl set id: c3fdbc5c-da70-4cbd-bdee-eddb4d852b26

Reported adverse events (FAERS/openFDA)#

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