Nitrous Oxide

Manufacturer
WSM SUPPLIER LLC.
Effective date
2025-10-08
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:00:25

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 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 PRESSURE; 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 get in eyes, on skin, or on clothing. Use and store only outdoors or in a well-ventilated place. Wear protective gloves, protective clothing, and either eye or face protection. In case of fire: Stop leak if safe to do so. Store locked up. Dispose of contents/container in accordance with container supplier/owner instructions. Use a back flow preventive device in the piping. Close valve after each use and when empty. Use only with equipment rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only equipment of compatible materials of construction. Open valve slowly. Use only with equipment cleaned for oxygen service. Protect from sunlight when ambient temperature exceeds 52 C (125 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

WARNING: Tis product can expose you to chemicals including Nitrous Oxide, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www. P65Warnings.ca.gov

WSM SUPPLIER LLC

3535 NW 60th Street

Miami FL 33142 (305) 455 1220

www.wsmsupplier.com nitrous 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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84120-003-01Nitrous Oxide1337 L in 1 CYLINDERGAS13373
84120-003-02Nitrous Oxide2978 L in 1 CYLINDERGAS29783
84120-003-03Nitrous Oxide4073 L in 1 CYLINDERGAS40733
84120-003-04Nitrous Oxide6139 L in 1 CYLINDERGAS61393
84120-003-05Nitrous Oxide8267 L in 1 CYLINDERGAS82673
84120-003-06Nitrous Oxide10090 L in 1 CYLINDERGAS100903
84120-003-07Nitrous Oxide16047 L in 1 CYLINDERGAS160473
84120-003-08Nitrous Oxide18175 L in 1 CYLINDERGAS181753
84120-003-09Nitrous Oxide535 L in 1 CYLINDERGAS5353
84120-003-10Nitrous Oxide1070 L in 1 CYLINDERGAS10703
84120-003-11Nitrous Oxide1745 L in 1 CYLINDERGAS17453
84120-003-12Nitrous Oxide711 L in 1 CYLINDERGAS7113
84120-003-13Nitrous Oxide5167 L in 1 CYLINDERGAS51673
84120-003-14Nitrous Oxide14163 L in 1 CYLINDERGAS141633
84120-003-15Nitrous Oxide18600 L in 1 CYLINDERGAS186003

Products#

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

DailyMed product names page 1 of 1 · 1 matching rows.

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-02full-release2026-05-31 21:18:30

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nitrous OxideNITROUS OXIDEMatheson Tri-Gas, Inc.f5f0f2f7-86a2-41f0-a6cd-3b8cb916dedd2025-12-02Exact identifier
ndc (product): 55037-301
Nitrous OxideNITROUS OXIDEWSM SUPPLIER LLC.17e334cc-a3af-d4f0-e063-6294a90ae41e2025-10-08Exact identifier
ndc (package): 84120-003-01
ndc (package): 84120-003-13
ndc (package): 84120-003-04
ndc (package): 84120-003-02
ndc (package): 84120-003-03
ndc (package): 84120-003-09
ndc (package): 84120-003-15
ndc (package): 84120-003-08
ndc (package): 84120-003-07
ndc (package): 84120-003-12
ndc (package): 84120-003-10
ndc (package): 84120-003-11
ndc (package): 84120-003-05
ndc (package): 84120-003-06
ndc (package): 84120-003-14
ndc (product): 84120-003
ndc11 (package): 84120000302
ndc11 (package): 84120000313
ndc11 (package): 84120000311
ndc11 (package): 84120000303
ndc11 (package): 84120000312
ndc11 (package): 84120000304
ndc11 (package): 84120000314
ndc11 (package): 84120000310
ndc11 (package): 84120000306
ndc11 (package): 84120000315
ndc11 (package): 84120000301
ndc11 (package): 84120000305
ndc11 (package): 84120000307
ndc11 (package): 84120000308
ndc11 (package): 84120000309
spl id: 40a9f90f-59ef-d5ca-e063-6294a90abc91
spl set id: 17e334cc-a3af-d4f0-e063-6294a90ae41e

Reported adverse events (FAERS/openFDA)#

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