Nitrous Oxide

Manufacturer
AIRGAS NOR PAC INC
Effective date
2011-05-06
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 20:11:53

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 UN1070 DO NOT REMOVE THIS PRODUCT LABEL.
NON-FLAMMABLE GAS 2      OXIDIZER  5.1   
834436 (12/04)  
Rx only. CAUTION: Federal law prohibits dispensing without prescription.
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.
WARNING: HIGH PRESSURE OXIDIZING LIQUID AND GAS. VIGOROUSLY ACCELERATES COMBUSTION. CAN CAUSE RAPID SUFFOCATION. CAN CAUSE ANESTHETIC EFFECTS. MAY CAUSE FROSTBITE. Avoid breathing gas. Store and use with adequate ventilation.  Keep oil and grease away. Use only with equipment cleaned for oxygen and rated for cylinder pressure. Do not get liquid in eyes, on skin, or clothing. Cylinder temperature should not exceed 52C (125F). Open valve slowly. Close valve after each use and when empty. Use a back flow preventive device in the piping. Use in accordance with the Material Safety Data Sheets (MSDS).
FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Call a physician. IN CASE OF FROSTBITE, obtain medical treatment immediately.
CAS: 10024-97-2
AIRGAS PURITAN MEDICAL Airgas Nor Pac, Inc. Vancouver, WA 98682 (360) 944-4000nitrous oxidenitrous oxide

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
347166nitrous oxide 99.2 % Gas for InhalationPSN3
347166nitrous oxide 99.2 % Gas for InhalationSCD3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57472-003-01Nitrous Oxide2464 L in 1 CYLINDERGAS24643
57472-003-02Nitrous Oxide4928 L in 1 CYLINDERGAS49283
57472-003-03Nitrous Oxide7392 L in 1 CYLINDERGAS73923
57472-003-04Nitrous Oxide91168 L in 1 CYLINDERGAS911683
57472-003-05Nitrous Oxide16016 L in 1 CYLINDERGAS160163
57472-003-06Nitrous Oxide15770 L in 1 CYLINDERGAS157703
57472-003-07Nitrous Oxide3696 L in 1 CYLINDERGAS36963
57472-003-08Nitrous Oxide12320 L in 1 CYLINDERGAS123203
57472-003-09Nitrous Oxide17989 L in 1 CYLINDERGAS179893
57472-003-10Nitrous Oxide1724 L in 1 CYLINDERGAS17243
57472-003-11Nitrous Oxide985 L in 1 CYLINDERGAS9853
57472-003-12Nitrous Oxide370 L in 1 CYLINDERGAS3703

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57472-003NITROUS OXIDE GAS [AIRGAS NOR PAC INC]3Legacy NDC, 12 package rows20110506_b528043b-5304-42d7-b892-5f9454c79c8d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Nitrous OxideACTIVE INGREDIENTK50XQU10293
Nitrous OxideACTIVE MOIETYK50XQU10293

Products#

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

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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
Nitrous OxideK50XQU1029ACTIB

Source Document#

Source XML

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
7881d7c9-ebea-4092-8b21-38d2b823ad17b528043b-5304-42d7-b892-5f9454c79c8d2011-05-06Exact identifier
spl id: 7881d7c9-ebea-4092-8b21-38d2b823ad17
spl set id: b528043b-5304-42d7-b892-5f9454c79c8d

Reported adverse events (FAERS/openFDA)#

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