FDA.reportPublic FDA data

nitrous oxide

Manufacturer
American Welding & Gas | American Welding & Gas, Inc.
Effective date
2026-10-08
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
20
Source
daily-update
Hydrated at
2026-10-13 04:09:22

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

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. 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 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 DO NOT REMOVE THIS PRODUCT LABEL.

AWG

AMERICAN WELDING AND GAS

1346 Monad Road, Billings, MT 59101

406.256.3344 nitrous oxidenitrous oxide

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROUS OXIDEACTIVE INGREDIENTK50XQU10292
NITROUS OXIDEACTIVE MOIETYK50XQU10292

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
44076-01244076-012-01, 44076-012-02, 44076-012-03, 44076-012-04, 44076-012-05, 44076-012-06, 44076-012-07, 44076-012-08, 44076-012-09, 44076-012-10, 44076-012-11, 44076-012-12, 44076-012-13, 44076-012-14

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
192026-05-21full-release2026-05-31 22:20:43
182025-10-28monthly-update2026-06-03 17:42:19
172025-09-16full-release2026-05-31 21:43:04

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 OXIDEAmerican Welding & Gas07aa2a86-d01e-470f-a12c-9908118bedc62026-10-08Exact identifier
ndc (package): 44076-012-01
ndc (package): 44076-012-10
ndc (package): 44076-012-09
ndc (package): 44076-012-02
ndc (package): 44076-012-11
ndc (package): 44076-012-04
ndc (package): 44076-012-06
ndc (package): 44076-012-14
ndc (package): 44076-012-08
ndc (package): 44076-012-05
ndc (package): 44076-012-13
ndc (package): 44076-012-07
ndc (package): 44076-012-12
ndc (package): 44076-012-03
ndc (product): 44076-012
ndc11 (package): 44076001210
ndc11 (package): 44076001208
ndc11 (package): 44076001201
ndc11 (package): 44076001213
ndc11 (package): 44076001202
ndc11 (package): 44076001211
ndc11 (package): 44076001207
ndc11 (package): 44076001214
ndc11 (package): 44076001206
ndc11 (package): 44076001203
ndc11 (package): 44076001209
ndc11 (package): 44076001204
ndc11 (package): 44076001212
ndc11 (package): 44076001205
spl id: 5d59027c-7ae1-b06d-e063-6294a90a92e3
spl set id: 07aa2a86-d01e-470f-a12c-9908118bedc6

Reported adverse events (FAERS/openFDA)#

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