NITROUS OXIDE

Manufacturer
Spectrum Gas Products, Inc | Spectrum Gas Products, Inc.
Effective date
2025-12-03
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 21:48:14

Label at a glance#

ProductNITROUS OXIDE
Active ingredientNITROUS OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

Nitrous Oxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE, 

USP  

Rx ONLY 

UN1070 

NON-FLAMMABLE GAS  2 SGP-26 OXIDIZER 5.1     

Spectrum Gas Products  

2381 E. Winston Road 

Anaheim, CA 92806 

Rx only. WARNING: Administration of Nitrous Oxide 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 Nitrous Oxide 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. DANGER: MAY CAUSE OR INTENSIFY FIRE, OXIDIZER. CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED. MAY CAUSE DROWSINESS OR DIZZINESS. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY CAUSE FROSTBITE. Do not handle until all safety precautions have been rad and understood. Keep and store away from clothing and other combustible materials. Keep valves ad fittings free from grease and oil. Avoid breathing gas. Do not get in eyes, on skin, or on clothing. Use and store only outdoors or in a well-ventilated place. In case of fire: Stop leak if safe to do so. Use a back-flow preventive device in the piping. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. Open valve slowly. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52oC (125oF). Read and follow the Safety Data Sheet (SDS) before use. FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER or doctor/physician if you feel unwell. IF ON SKIN:  Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention. CAS: 10024-97-2 DO NOT REMOVE THIS PRODUCT LABEL. 

Nitrous Oxide Shoulder LabelNitrous Oxide Shoulder Label

Nitrous Oxide Sidewall LabelNitrous Oxide Sidewall Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN5
312022nitrous oxide 99 % Gas for InhalationSCD5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67525-400-01NITROUS OXIDE1482 L in 1 CYLINDERGAS14825
67525-400-02NITROUS OXIDE4942 L in 1 CYLINDERGAS49425
67525-400-03NITROUS OXIDE7413 L in 1 CYLINDERGAS74135
67525-400-04NITROUS OXIDE12356 L in 1 CYLINDERGAS123565

Products#

Every source-derived product name is available through these pages.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67525-40067525-400-01, 67525-400-02, 67525-400-03, 67525-400-04

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
NITROUS OXIDEK50XQU1029ACTIB

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
NITROUS OXIDENITROUS OXIDESpectrum Gas Products, Incb550ebb2-e617-4913-8f75-1a07662e87e52025-12-03Exact identifier
ndc (package): 67525-400-03
ndc (package): 67525-400-02
ndc (package): 67525-400-04
ndc (package): 67525-400-01
ndc (product): 67525-400
ndc11 (package): 67525040003
ndc11 (package): 67525040001
ndc11 (package): 67525040002
ndc11 (package): 67525040004
spl id: 450fd993-6aa5-df41-e063-6394a90aaef6
spl set id: b550ebb2-e617-4913-8f75-1a07662e87e5

Reported adverse events (FAERS/openFDA)#

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