Nitrous Oxide
- Manufacturer
- Roberts Oxygen Company, Inc.
- Effective date
- 2025-11-17
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 9
- Source
- full-release
- Hydrated at
- 2026-05-31 21:46:26
Label at a glance#
ProductNitrous Oxide
Active ingredientNITROUS OXIDE
Label structure1 sections
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NITROUS
OXIDE,
REFRIGERATED
LIQUID
USP
UN2201
NON-FLAMMABLE GAS 2
OXIDIZER 5.1
Roberts Oxygen Company, Inc
P.O. BOX 5507 Rockville, MD 20855
301-948-8100
↑ALWAYS KEEP CONTAINER IN UPRIGHT POSITION↑
WARNING:
Rx Only. Administration of Nitrous Oxide USP 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 USP and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and the hazards, contraindications and side effects and the precautions to be taken.
DANGER: MAY CAUSE OR INTENSIFY FIRE; OXIDIZER. CONTAINS REFRIGERATED GAS; MAY CAUSE CRYOGENIC BURNS OR INJURY. MAY CAUSE DROWSINESS OR DIZZINESS. MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION. Do not handle until all safety precautions have been read and understood. Keep and store away from clothing and other combustible materials. Keep valves and fitting free from grease and oil. Avoid breathing gas. Use and store only outdoors or in a well-ventilated place. Wear cold insulating gloves, face shield, and eye protection. In case of fire: Stop leak if safe to do so. Use a back flow preventative device in the piping. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Use only with equipment cleaned for oxygen service. Avoid spills. Do not walk or roll equipment over spills. Close valve after each use and when empty. Read and follow the Safety Data Sheet (SDS) before use.
FIRST AID: IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a
POISON CENTER or doctor/physician if you feel unwell.
IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.
CAS: 10024-97-2
DO NOT REMOVE THIS PRODUCT LABEL.
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 46123-007-01 | Nitrous Oxide | 91453 L in 1 DEWAR | GAS | 91453 | 9 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Nitrous Oxide | ACTIVE INGREDIENT | K50XQU1029 | 1 | |
| Nitrous Oxide | ACTIVE MOIETY | K50XQU1029 | 1 |
Products#
Every source-derived product name is available through these pages.
- Nitrous Oxide
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 46123-007 | 46123-007-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| NITROUS OXIDE | K50XQU1029 | ACTIB |
Source Document#
Orange Book application contexts#
All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Nitrous Oxide | NITROUS OXIDE | Roberts Oxygen Company, Inc. | aaa2ed08-c5cb-4d46-917b-ce1a9d0ce462 | 2025-11-17 | 46123-007-01 46123-007 46123000701 43cf2922-0d64-62b2-e063-6394a90ad7a7 aaa2ed08-c5cb-4d46-917b-ce1a9d0ce462 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.