NITROUS OXIDE

Manufacturer
Compressed Gases Inc
Effective date
2010-01-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:09:19

Label at a glance#

ProductNITROUS OXIDE
Active ingredientNITROUS OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

NITROUS OXIDE USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE U.S.P.  UN 1070  NON-FLAMMABLE-2  OXIDIZER-5.1

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, METHODS, AND FREQUENCY AND DURATION OF ADMINISTRATION AND WITH THE HAZARDS, CONTRAINDICATIONS AND SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN.

CAUTION: Rx ONLY.  FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION.

GROSS WT________________ LBS____________ OZ

TARE WT ________________ LBS ______________ OZ

NET WT. _________________ LBS _______________ OZ

SIZE _______________ CONTENTS___________LITERS_____________

7025R1  5/04

NITROUS LABELNITROUS LABEL

PRODUCT 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 AND DESIGNATED FOR NITROUS OXIDE SERVICE 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.  USER SHALL SECURE CYLINDER IN USE AND IN STORAGE.  USE IN UPRIGHT POSITION.  KEEP VALVE PROTECTION CAP IN PLACE WHEN NOT IN USE IF SO EQUIPPED.  USE IN ACCORDANCE WITH MSDS.  RETURN WITH 25 PSIG. 

NOTE: SUCK-BACK INTO CYLINDER MAY CAUSE RUPTURE.  ALWAYS USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING.

CAUTION: Rx ONLY.  FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. 

WARNING: BREATHING PURE NITROUS OXIDE CAN CAUSE DEATH BY RAPID SUFFOCATION. 

FIRST AID:  IF INHALED  REMOVE TO FRESH AIR.  IF NOT BREATHING GIVE ARTIFICIAL RESPIRATION.  IF BREATHING IS 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
34330-003-01NITROUS OXIDE700 L in 1 CYLINDERGAS7001
34330-003-02NITROUS OXIDE1989 L in 1 CYLINDERGAS19891
34330-003-03NITROUS OXIDE3280 L in 1 CYLINDERGAS32801
34330-003-04NITROUS OXIDE6281 L in 1 CYLINDERGAS62811
34330-003-05NITROUS OXIDE6896 L in 1 CYLINDERGAS68961

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
34330-003NITROUS OXIDE GAS [COMPRESSED GASES INC]1Legacy NDC, 5 package rows20100719_cb9be40a-1e3a-4dce-8eae-f9617a8a765c.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
34330-00334330-003-01, 34330-003-02, 34330-003-03, 34330-003-04, 34330-003-05

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
c4b4e135-e6dc-4ee0-b7e8-03c081ca8ebbcb9be40a-1e3a-4dce-8eae-f9617a8a765c2010-01-01WarningsExact identifier
spl id: c4b4e135-e6dc-4ee0-b7e8-03c081ca8ebb
spl set id: cb9be40a-1e3a-4dce-8eae-f9617a8a765c

Reported adverse events (FAERS/openFDA)#

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