Nitrous Oxide

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Nitrous Oxide
Generic name: NITROUS OXIDE
Manufacturer: Roberts Oxygen Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: aaa2ed08-c5cb-4d46-917b-ce1a9d0ce462
SPL ID: 43cf2922-0d64-62b2-e063-6394a90ad7a7
Version: 9
Effective date: 2025-11-17
Source export date: 2026-10-30
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:34:39

Harmonized routes table
Harmonized routes
RESPIRATORY (INHALATION)

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	NDA	206009	derived:openfda.application_number
application number		NDA206009	openfda.application_number
brand name		Nitrous Oxide	openfda.brand_name
generic name		NITROUS OXIDE	openfda.generic_name
manufacturer name		Roberts Oxygen Company, Inc.	openfda.manufacturer_name
ndc	package	46123-007-01	openfda.package_ndc
ndc	product	46123-007	openfda.product_ndc
ndc11	package	46123000701	derived:openfda.package_ndc
rxcui		312022	openfda.rxcui
spl id		43cf2922-0d64-62b2-e063-6394a90ad7a7	id
spl set id		aaa2ed08-c5cb-4d46-917b-ce1a9d0ce462	set_id
unii		K50XQU1029	openfda.unii

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