FDA.reportPublic FDA data

Nitrous Oxide

Manufacturer
ILMO Products Company
Effective date
2025-10-29
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
16
Source
full-release
Hydrated at
2026-05-31 22:03:39

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 DO NOT REMOVE THIS LABEL.
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 CAUSE 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. WARNING: This product contains a chemical known to the state of California to cause birth defects or other reproductive harm. CAS: 10024-97-2
ILMO 7 EASTGATE DRIVE JACKSONVILLE, ILLINOIS 62650 217-245-2183 nitrous oxide 1nitrous oxide 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN16
312022nitrous oxide 99 % Gas for InhalationSCD16

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51486-007-01Nitrous Oxide15770 L in 1 CYLINDERGAS1577016
51486-007-02Nitrous Oxide4928 L in 1 CYLINDERGAS492816
51486-007-03Nitrous Oxide1725 L in 1 CYLINDERGAS172516
51486-007-04Nitrous Oxide8267 L in 1 CYLINDERGAS826716
51486-007-05Nitrous Oxide14163 L in 1 CYLINDERGAS1416316
51486-007-06Nitrous Oxide1720 L in 1 CYLINDERGAS172016
51486-007-07Nitrous Oxide16047 L in 1 CYLINDERGAS1604716
51486-007-08Nitrous Oxide5167 L in 1 CYLINDERGAS516716

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
51486-00751486-007-01, 51486-007-02, 51486-007-03, 51486-007-04, 51486-007-05, 51486-007-06, 51486-007-07, 51486-007-08

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
152025-01-14full-release2026-05-31 21:22:49

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 OXIDEILMO Products Companybc5b4097-9292-41a2-82bb-30671b9ecf422025-10-29Exact identifier
ndc (package): 51486-007-06
ndc (package): 51486-007-04
ndc (package): 51486-007-03
ndc (package): 51486-007-08
ndc (package): 51486-007-05
ndc (package): 51486-007-07
ndc (package): 51486-007-01
ndc (package): 51486-007-02
ndc (product): 51486-007
ndc11 (package): 51486000703
ndc11 (package): 51486000706
ndc11 (package): 51486000707
ndc11 (package): 51486000701
ndc11 (package): 51486000704
ndc11 (package): 51486000702
ndc11 (package): 51486000708
ndc11 (package): 51486000705
spl id: 424c9dbb-3e1d-e00f-e063-6294a90a74b2
spl set id: bc5b4097-9292-41a2-82bb-30671b9ecf42

Reported adverse events (FAERS/openFDA)#

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