Nitrogen

Manufacturer
TULSA GAS & GEAR, LLC
Effective date
2018-11-05
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:47:50

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 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 LABLE.
TULSA GAS & GEAR
6665 S 65TH W AVE
TULSA, OK 74131-2420
918-447-4411 nitrogennitrogen

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71707-00271707-002-01, 71707-002-02, 71707-002-03, 71707-002-04

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

Orange Book application contexts#

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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
79f0eabe-87c7-a0f5-e053-2a91aa0a383cbe31e9fd-35f1-4404-9d12-9ba29d0d61242018-11-05Exact identifier
spl id: 79f0eabe-87c7-a0f5-e053-2a91aa0a383c
spl set id: be31e9fd-35f1-4404-9d12-9ba29d0d6124

Reported adverse events (FAERS/openFDA)#

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