Nitrous Oxide

Manufacturer
Oxarc, LLC
Effective date
2025-11-25
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
17
Source
full-release
Hydrated at
2026-05-31 21:47:14

Label at a glance#

ProductNitrous Oxide
Active ingredientNITROUS OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE USP NON-FLAMMABLE GAS 2 OXIDIZER 5.1 UN1070
OXARC 4003 E BROADWAY SPOKANE, WA 99202 1-800-536-9272 www.oxarc.com
Rx only. WARNING: Administration of Nitrous Oxide 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 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 PESSURE; MAY EXPLODE IF HEATED. MAY CUASE DROWSINESS OR DIZZINESS. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. MAY CAUSE FROSTBITE. Do not handle until all safety precautions have been read and understood. Keep and store away from clothing and other combustible materials. Keep valves and fittings free from grease and oil. Avoid breathing gas. Do not put 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 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. 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 LABEL
Size Contents Size Contents AND 1.74 Liters 50# 18.51 Liters ANE 2.36 Liters 64# 23.69 Liters 20# 7.4 Liters 75# 27.76 Liters Other Liters nitrousoxide1nitrousoxide1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN17
312022nitrous oxide 99 % Gas for InhalationSCD17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
34057-010-01Nitrous Oxide906 L in 1 CYLINDERGAS90617
34057-010-02Nitrous Oxide1557 L in 1 CYLINDERGAS155717
34057-010-03Nitrous Oxide4814 L in 1 CYLINDERGAS481417
34057-010-04Nitrous Oxide12063 L in 1 CYLINDERGAS1206317
34057-010-05Nitrous Oxide15461 L in 1 CYLINDERGAS1546117
34057-010-06Nitrous Oxide18123 L in 1 CYLINDERGAS1812317

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Nitrous OxideACTIVE INGREDIENTK50XQU10294
Nitrous OxideACTIVE MOIETYK50XQU10294

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
34057-01034057-010-01, 34057-010-02, 34057-010-03, 34057-010-04, 34057-010-05, 34057-010-06

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 OXIDEOxarc, LLC56d37fcb-8abf-4671-9388-a8837c94e5a22025-11-25Exact identifier
ndc (package): 34057-010-05
ndc (package): 34057-010-04
ndc (package): 34057-010-03
ndc (package): 34057-010-01
ndc (package): 34057-010-02
ndc (package): 34057-010-06
ndc (product): 34057-010
ndc11 (package): 34057001001
ndc11 (package): 34057001003
ndc11 (package): 34057001006
ndc11 (package): 34057001005
ndc11 (package): 34057001002
ndc11 (package): 34057001004
spl id: 4475d50c-af27-b545-e063-6294a90a6b20
spl set id: 56d37fcb-8abf-4671-9388-a8837c94e5a2

Reported adverse events (FAERS/openFDA)#

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