Nitrogen

Manufacturer
C & C Oxygen Company
Effective date
2026-10-19
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
24
Source
daily-update
Hydrated at
2026-10-22 02:05:30

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
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 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.
C&C OXYGEN CO.
3615 ROSSVILLE BLVD
CHATTANOOGA, TN 37407
800-424-9300 nitrogenonenitrogenone

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REFRIGERATED LIQUID
NITROGEN, REFRIGERATED LIQUID NF UN1977
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 insulation 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
DO NOT REMOVE THIS PRODUCT LABEL.
C&C OXYGEN CO.
3615 ROSSVILLE BLVD
CHATTANOOGA, TN 37407
800-424-9300 nitrogen liquidnitrogen liquid

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROGENACTIVE INGREDIENTN762921K7512
NITROGENACTIVE MOIETYN762921K7512

Products#

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NDC Codes#

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
232025-10-28full-release2026-05-31 22:03:17
222024-12-16full-release2026-05-31 21:19:41

Orange Book application contexts#

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openFDA label cross-check#

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Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NitrogenNITROGENC & C Oxygen Company32d9050e-dc65-48b9-bfee-b914d38481272025-10-28Exact identifier
ndc (package): 50322-003-13
ndc (package): 50322-003-01
ndc (package): 50322-003-10
ndc (package): 50322-003-09
ndc (package): 50322-003-07
ndc (package): 50322-003-12
ndc (package): 50322-003-06
ndc (package): 50322-003-02
ndc (package): 50322-003-05
ndc (package): 50322-003-04
ndc (package): 50322-003-11
ndc (package): 50322-003-03
ndc (package): 50322-003-08
ndc (product): 50322-003
ndc11 (package): 50322000301
ndc11 (package): 50322000303
ndc11 (package): 50322000310
ndc11 (package): 50322000308
ndc11 (package): 50322000304
ndc11 (package): 50322000305
ndc11 (package): 50322000307
ndc11 (package): 50322000312
ndc11 (package): 50322000311
ndc11 (package): 50322000309
ndc11 (package): 50322000313
ndc11 (package): 50322000306
ndc11 (package): 50322000302
spl set id: 32d9050e-dc65-48b9-bfee-b914d3848127

Reported adverse events (FAERS/openFDA)#

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