FDA.reportPublic FDA data

Nitrous Oxide

Manufacturer
Lessors, Incorporated
Effective date
2025-10-13
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
18
Source
full-release
Hydrated at
2026-05-31 22:01:07

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 2 OXIDIZER 5.1

34436 (R04/05)
Rx only. WARNING: Administration of Nitrous Oxide may be hazardous or contraindicated. For use 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 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.
LESSORS, INC. 1300 N. GENESEE RD BURTON, MI 48509 810-742-2302 nitrousoxidenitrousoxide

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN18
312022nitrous oxide 99 % Gas for InhalationSCD18

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55404-002-01Nitrous Oxide242 L in 1 CYLINDERGAS24218
55404-002-02Nitrous Oxide940 L in 1 CYLINDERGAS94018
55404-002-03Nitrous Oxide1560 L in 1 CYLINDERGAS156018
55404-002-04Nitrous Oxide3630 L in 1 CYLINDERGAS363018
55404-002-05Nitrous Oxide4840 L in 1 CYLINDERGAS484018
55404-002-06Nitrous Oxide16550 L in 1 CYLINDERGAS1655018
55404-002-07Nitrous Oxide15490 L in 1 CYLINDERGAS1549018

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
55404-00255404-002-01, 55404-002-02, 55404-002-03, 55404-002-04, 55404-002-05, 55404-002-06, 55404-002-07

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
172024-11-07full-release2026-05-31 21:16:43

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 OXIDELessors, Incorporatedb18bf991-bc6e-4678-99c0-61d7cbdb171a2025-10-13Exact identifier
ndc (package): 55404-002-07
ndc (package): 55404-002-06
ndc (package): 55404-002-02
ndc (package): 55404-002-05
ndc (package): 55404-002-03
ndc (package): 55404-002-04
ndc (package): 55404-002-01
ndc (product): 55404-002
ndc11 (package): 55404000205
ndc11 (package): 55404000204
ndc11 (package): 55404000201
ndc11 (package): 55404000202
ndc11 (package): 55404000206
ndc11 (package): 55404000203
ndc11 (package): 55404000207
spl id: 410d77e3-f9bd-66e2-e063-6394a90a781d
spl set id: b18bf991-bc6e-4678-99c0-61d7cbdb171a

Reported adverse events (FAERS/openFDA)#

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