Nitrous Oxide

Manufacturer
ILMO Products Company
Effective date
2010-12-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:51:57

Label at a glance#

ProductNitrous Oxide
Active ingredientNitrous Oxide
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE
USP
UN1070
NON-FLAMMABLE GAS         2
OXIDIZER     5.1
34436     (R04/05)
Rx ONLY. 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. 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 oxygen and rated for cylinder pressure. Do not get liquid in eyes, on skin or clothing. Cylinder temperature should not exceed 52 degrees C (125 degrees F). Open valve slowly. Close valve after each use and when empty. Use a back flow preventive device in the piping. 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 is difficult, give oxygen. Call a physician. IN CASE OF FROSTBITE, obtain medical treatment immediately.
CAS NUMBER: 10024-97-2
DO NOT REMOVE THIS PRODUCT LABEL.
ILMO PRODUCTS COMPANY
JACKSONVILLE, IL 62650     WWW.ILMOPRODUCTS.COM
IN CASE OF CHEMICAL EMERGENCY CALL 1-800-424-9300nitrous oxide onenitrous oxide one

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NITROUS OXIDE
USP
UN1070
NON-FLAMMABLE GAS 2
OXIDIZER 5.1
CONTENTS:_____________________
LOT NO: __________________________
Rx Only.
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.
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 oxygen and rated for cylinder pressure.
Do not get liquid in eyes, on skin or clothing.
Cylinder temperature should not exceed 52 degrees C (125 degrees F).
Open valve slowly.
Close valve after each use and when empty.
Use a back flow preventive device in the piping.
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 is difficult, give oxygen. Call a physician.
IN CASE OF FROSTBITE, obtain medical treatment immediately.
CAS: 10024-97-2
DO NOT REMOVE THIS PRODUCT LABEL.
CYLINDER INSPECTED AND FILLED BY
ILMO PRODUCTS CO.
7 EASTGATE DRIVE JACKSONVILLE, ILLINOIS 62650
Store/Service Locations:
IL: Decatur, Jacksonville, Litchfield, Mattoon, Mt. Vernon, Peoria, Springfield, Quincy
MO: St. Louis/Fenton    
In case of emergency call 1-800-424-9300
47142
(05/09)nitrous oxide twonitrous oxide two

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Nitrous OxideACTIVE INGREDIENTK50XQU10291
Nitrous OxideACTIVE MOIETYK50XQU10291

Products#

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DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51486-00351486-003-01, 51486-003-02, 51486-003-03

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
07db80ac-19f7-22e7-e063-6394a90a6fc56f582303-22c1-4237-bed5-94664295beee2023-10-16Exact identifier
spl set id: 6f582303-22c1-4237-bed5-94664295beee

Reported adverse events (FAERS/openFDA)#

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