NITROUS OXIDE

Manufacturer
Holston Gases, Inc
Effective date
2010-01-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:09:00

Label at a glance#

ProductNITROUS OXIDE
Active ingredientNITROUS OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

NITROUS OXIDE COMPRESSED LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE, COMPRESSED - NON-FLAMMABLE GAS - 2 - OXIDIZER USP UN 1070

WARNING SECURE ALL CYLINDERS WHILE IN STORAGE AND IN USE.

CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION

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.

NITROUS LABELNITROUS LABEL

GENERAL WARNINGS AND PRECAUTIONS

WARNINGS AND PRECAUTIONS SECTION

WARNING: HIGH PRESSURE OXIDIZING LIQUID AND GAS.  VIGOROUSLY ACCELERATES COMBUSTION.  CAN CAUSE RAPID SUFFOCATION.  CAN CAUSE ANESTHETIC EFFECTS.  MAY CAUSE FROSTBITE.  AVOID BREATHING GAS.  STORE AND USE WITH ADEQUATE VENTILATION. KEEP OIL AND GREASE AWAY.  USE ONLY WITH EQUIPMENT CLEANED FOR NITROUS OXIDE AND RATED FOR CYLINDER PRESSURE.  DO NOT GET LIQUID IN EYES ON SKIN OR CLOTHING.  CYLINDER TEMPERATURE SHOULD NOT EXCEED 125 F (52 C)  OPEN VALVE SLOWLY  CLOSE VALVE AFTER EACH USE AND WHEN EMPTY.  USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS)  NOTE: SUCK-BACK INTO CYLINDER MAY CAUSE RUPTURE.  ALWAYS USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING.  FIRST AID: IF INHALED REMOVE TO FRESH AIR.  IF NOT BREATHING GIVE ARTIFICIAL RESPIRATION.  IF BREATHING DIFFICULT GIVE OXYGEN.  CALL A PHYSICIAN.  IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY.

DO NOT REMOVE THIS PRODUCT LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312022nitrous oxide 99 % Gas for InhalationPSN1
312022nitrous oxide 99 % Gas for InhalationSCD1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55050-0008-1NITROUS OXIDE2.90 kg in 1 CYLINDERGAS2.901
55050-0008-2NITROUS OXIDE9.07 kg in 1 CYLINDERGAS9.071
55050-0008-3NITROUS OXIDE25.4 kg in 1 CYLINDERGAS25.41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55050-0008NITROUS OXIDE GAS [HOLSTON GASES, INC]1Legacy NDC, 3 package rows20100719_213779ba-ba2f-4d5f-83bf-d57951d6bdb4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
NITROUS OXIDEACTIVE INGREDIENTK50XQU10291
NITROUS OXIDEACTIVE MOIETYK50XQU10291

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
55050-000855050-0008-1, 55050-0008-2, 55050-0008-3

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
8f26ed93-327d-468a-ac00-c11e6aab2027213779ba-ba2f-4d5f-83bf-d57951d6bdb42010-01-01WarningsExact identifier
spl id: 8f26ed93-327d-468a-ac00-c11e6aab2027
spl set id: 213779ba-ba2f-4d5f-83bf-d57951d6bdb4

Reported adverse events (FAERS/openFDA)#

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