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: Nitrous Oxide
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 2b0b9cc4-fca7-4e84-8d9d-0f9852528579
SPL ID: 4358f26d-144b-9a1d-e063-6394a90ac2b5
Version: 16
Effective date: 2025-11-11
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:01

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		Nitrous Oxide	openfda.manufacturer_name
ndc	package	54260-001-01	openfda.package_ndc
ndc	product	54260-001	openfda.product_ndc
ndc11	package	54260000101	derived:openfda.package_ndc
rxcui		312022	openfda.rxcui
spl id		4358f26d-144b-9a1d-e063-6394a90ac2b5	id
spl set id		2b0b9cc4-fca7-4e84-8d9d-0f9852528579	set_id
unii		K50XQU1029	openfda.unii

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