Nitrous Oxide

Manufacturer
Welding & Therapy Service, Inc
Effective date
2011-07-22
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 20:12:24

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

NON-FLAMMABLE GAS 2      OXIDIZER 5.1

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.  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 52oC (125oF).  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 Sheet (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                                                                                    DO NOT REMOVE THIS PRODUCT LABEL
Image of Nitrous Oxide labelImage of Nitrous Oxide label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN6
312022nitrous oxide 99 % Gas for InhalationSCD6

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
33344-003-01Nitrous Oxide940 L in 1 CYLINDERGAS9406
33344-003-02Nitrous Oxide1590 L in 1 CYLINDERGAS15906
33344-003-03Nitrous Oxide5098 L in 1 CYLINDERGAS50986
33344-003-04Nitrous Oxide8156 L in 1 CYLINDERGAS81566
33344-003-05Nitrous Oxide14103 L in 1 CYLINDERGAS141036

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33344-003NITROUS OXIDE GAS [WELDING & THERAPY SERVICE, INC]6Legacy NDC, 5 package rows20110722_fa835c4c-a45c-4443-a6e5-995bfcccd587.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Nitrous OxideACTIVE INGREDIENTK50XQU10296
Nitrous OxideACTIVE MOIETYK50XQU10296

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
33344-00333344-003-01, 33344-003-02, 33344-003-03, 33344-003-04, 33344-003-05

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
a7819865-1852-46db-bbdb-75346d5339ecfa835c4c-a45c-4443-a6e5-995bfcccd5872011-07-22Exact identifier
spl id: a7819865-1852-46db-bbdb-75346d5339ec
spl set id: fa835c4c-a45c-4443-a6e5-995bfcccd587

Reported adverse events (FAERS/openFDA)#

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