FDA.reportPublic FDA data

Nitrogen

Manufacturer
SYOXSA, Inc.
Effective date
2025-12-12
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
13
Source
full-release
Hydrated at
2026-05-31 21:50:03

Label at a glance#

ProductNitrogen
Active ingredientNITROGEN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROGEN, COMPRESSED NF
UN1066
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 outdoor 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 Date 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.
SYOXSA
SYOXSA, INC.
6996 COMMERCE AVE. EL PASO, TX 79915
915-771-7674 nitrogennitrogen

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
311998nitrogen 99 % Gas for InhalationPSN13
311998nitrogen 99 % Gas for InhalationSCD13

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23647-002-01Nitrogen8608 L in 1 CYLINDERGAS860813
23647-002-02Nitrogen6512 L in 1 CYLINDERGAS651213
23647-002-03Nitrogen2265 L in 1 CYLINDERGAS226513
23647-002-04Nitrogen8501 L in 1 CYLINDERGAS850113
23647-002-05Nitrogen6453 L in 1 CYLINDERGAS645313
23647-002-06Nitrogen2240 L in 1 CYLINDERGAS224013
23647-002-07Nitrogen1052 L in 1 CYLINDERGAS105213

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
23647-00223647-002-01, 23647-002-02, 23647-002-03, 23647-002-04, 23647-002-05, 23647-002-06, 23647-002-07

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
NitrogenNITROGENSYOXSA, Inc.66b47ed5-82d0-44ba-a2aa-17db9b98ee222025-12-12Exact identifier
ndc (package): 23647-002-06
ndc (package): 23647-002-04
ndc (package): 23647-002-02
ndc (package): 23647-002-05
ndc (package): 23647-002-03
ndc (package): 23647-002-01
ndc (package): 23647-002-07
ndc (product): 23647-002
ndc11 (package): 23647000207
ndc11 (package): 23647000206
ndc11 (package): 23647000202
ndc11 (package): 23647000201
ndc11 (package): 23647000205
ndc11 (package): 23647000204
ndc11 (package): 23647000203
spl id: 45c700db-8d21-cf27-e063-6394a90a8c4f
spl set id: 66b47ed5-82d0-44ba-a2aa-17db9b98ee22

Reported adverse events (FAERS/openFDA)#

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