Nitrous Oxide
- Manufacturer
- AIRGAS NOR PAC INC
- Effective date
- 2011-05-06
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 20:11:53
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NITROUS OXIDE USP UN1070 DO NOT REMOVE THIS PRODUCT LABEL.
NON-FLAMMABLE GAS 2 OXIDIZER 5.1
834436 (12/04)
Rx only. CAUTION: Federal law prohibits dispensing without 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.
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 52C (125F). 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 Sheets (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
AIRGAS PURITAN MEDICAL Airgas Nor Pac, Inc. Vancouver, WA 98682 (360) 944-4000
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57472-003-01 | Nitrous Oxide | 2464 L in 1 CYLINDER | GAS | 2464 | 3 | |
| 57472-003-02 | Nitrous Oxide | 4928 L in 1 CYLINDER | GAS | 4928 | 3 | |
| 57472-003-03 | Nitrous Oxide | 7392 L in 1 CYLINDER | GAS | 7392 | 3 | |
| 57472-003-04 | Nitrous Oxide | 91168 L in 1 CYLINDER | GAS | 91168 | 3 | |
| 57472-003-05 | Nitrous Oxide | 16016 L in 1 CYLINDER | GAS | 16016 | 3 | |
| 57472-003-06 | Nitrous Oxide | 15770 L in 1 CYLINDER | GAS | 15770 | 3 | |
| 57472-003-07 | Nitrous Oxide | 3696 L in 1 CYLINDER | GAS | 3696 | 3 | |
| 57472-003-08 | Nitrous Oxide | 12320 L in 1 CYLINDER | GAS | 12320 | 3 | |
| 57472-003-09 | Nitrous Oxide | 17989 L in 1 CYLINDER | GAS | 17989 | 3 | |
| 57472-003-10 | Nitrous Oxide | 1724 L in 1 CYLINDER | GAS | 1724 | 3 | |
| 57472-003-11 | Nitrous Oxide | 985 L in 1 CYLINDER | GAS | 985 | 3 | |
| 57472-003-12 | Nitrous Oxide | 370 L in 1 CYLINDER | GAS | 370 | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Nitrous Oxide | ACTIVE INGREDIENT | K50XQU1029 | 3 | |
| Nitrous Oxide | ACTIVE MOIETY | K50XQU1029 | 3 |
Products#
Every source-derived product name is available through these pages.
- Nitrous Oxide
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 57472-003 | 57472-003-01, 57472-003-02, 57472-003-03, 57472-003-04, 57472-003-05, 57472-003-06, 57472-003-07, 57472-003-08, 57472-003-09, 57472-003-10, 57472-003-11, 57472-003-12 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Nitrous Oxide | K50XQU1029 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 7881d7c9-ebea-4092-8b21-38d2b823ad17 | b528043b-5304-42d7-b892-5f9454c79c8d | 2011-05-06 | 7881d7c9-ebea-4092-8b21-38d2b823ad17 b528043b-5304-42d7-b892-5f9454c79c8d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
