FDA.reportPublic FDA data

Nitrous Oxide

Manufacturer
Fullerton Welding Supply
Effective date
2013-01-18
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 20:16:25

Label at a glance#

ProductNitrous Oxide
Active ingredientNITROUS OXIDE
Label structure1 sections

Label contents#

Full prescribing information#

Principal for Nitrous Oxide Product

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEWLABELS.jpgNEWLABELS.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN3
312022nitrous oxide 99 % Gas for InhalationSCD3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42751-1070-12019-11-27C16284748780-19855d018-d8f8-cd31-e053-dbdaa90ab51aNitrous Oxide
42751-1070-22019-11-27C16284748780-19855d018-d8f8-cd31-e053-dbdaa90ab51aNitrous Oxide

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42751-1070-1Nitrous Oxide19.85 L in 1 CYLINDERGAS19.853
42751-1070-2Nitrous Oxide21.84 L in 1 CYLINDERGAS21.843

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42751-1070NITROUS OXIDE GAS [FULLERTON WELDING SUPPLY]3Legacy NDC, 2 package rows20130118_8f0149cb-5f7f-4c6e-99ce-ceaaf3d99466.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROUS OXIDEACTIVE INGREDIENTK50XQU10293
NITROUS OXIDEACTIVE MOIETYK50XQU10293

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
42751-107042751-1070-1, 42751-1070-2

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
a07b5b9a-5739-442e-978f-e7f2c77b49468f0149cb-5f7f-4c6e-99ce-ceaaf3d994662013-01-18Exact identifier
spl id: a07b5b9a-5739-442e-978f-e7f2c77b4946
spl set id: 8f0149cb-5f7f-4c6e-99ce-ceaaf3d99466

Reported adverse events (FAERS/openFDA)#

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