NITROUS OXIDE

Manufacturer
Argyle Welding Supply Co. Inc.
Effective date
2010-01-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:51

Label at a glance#

ProductNITROUS OXIDE
Active ingredientNITROUS OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

NITROUS OXIDE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE USP UN 1070  NON-FLAMMABLE GAS-2 OXIDIZER-5.1

Rx ONLY.  ADMINISTRATION OF NITROUS OXIDE MAY BE HAZARDOUS OR CONTRAINDICATED.  FOR USE ONLY BY OUR 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 AN SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN. 

CONTENTS__________ LITERS ______________ CU FT

37736 (06/05)

SHOULDER LABELSHOULDER 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 for nitrous oxide service and rated for cylinder pressure Do not get liquid in eyes, on skin, or clothing.  Cylinder temperature should not exceed 52 C (125 F)  Open valve slowly  Close valve when not in use and when empty. USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS)  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.  CAS 10024-97-2

FDA-Initiated Inactive NDC Indexing#

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
44397-01044397-010-01, 44397-010-02, 44397-010-03, 44397-010-04

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
4192711b-9c35-4bff-9f82-52298a6390b9b68099da-e93e-404a-84ff-41744b2c1c2a2021-12-20Exact identifier
spl set id: b68099da-e93e-404a-84ff-41744b2c1c2a

Reported adverse events (FAERS/openFDA)#

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