Nitrous Oxide

Manufacturer: Linde Gas & Equipment Inc. | Linde Gas & Equipment Inc
Effective date: 2026-05-14
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 12
Source: daily-update
Hydrated at: 2026-06-16 05:10:33

Label at a glance#

ProductNITROUS OXIDE

Active ingredientNITROUS OXIDE

Label structure1 sections

Contacts and useful links#

PhoneLabel contact1-800-645-4633

Label contents#

Full prescribing information#

NITROUS OXIDE USP LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

UN1070

NITROUS OXIDE, USP

DANGER!

MAY CAUSE OR INTENSIFY FIRE; OXIDIZER.

CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED.

MAY CAUSE DROWSINESS OR DIZZINESS.

MAY DISPLACE OXYGEN AND CAUSE RAPID SUFFOCATION.

MAY CAUSE FROSTBITE.

IN CASE OF EMERGENCY: CALL 1-800-645-4633

CAS: 10024-97-2

Do not handle until all safety precautions have been read and understood. Keep/Store away from combustible materials, clothing. Keep reduction valves/valves and fittings free from oil and grease. Avoid breathing gas. Do not get in eyes, on skin, or on clothing. Use and store only outdoors or in a well-ventilated place. Wear protective gloves/protective clothing/eye protection/face protection. IN CASE OF FIRE: Stop leak if safe to do so. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations. Contact supplier for any special requirements. Use a backflow preventative device in the piping. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Do not open valve until connected to equipment prepared for use. Use only with equipment cleaned for oxygen service. Open valve slowly. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52°C (125°F). Read and follow the Safety Data Sheet (SDS) before use.

FIRST AID: IF INHALED: remove victim to fresh air and keep at rest in a position comfortable for breathing. Call a POISON CENTER/doctor is you feel unwell.

IF ON SKIN: Thaw frosted parts with lukewarm water. Do you rub affected area. Get immediate medical advice/attention.

WARNING! Administration of nitrous oxide may be hazardous or contraindicated. For use only by or under 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.

Rx ONLY

Medipure by Linde

Linde

MDB-0004 (Rev. 01) DO NOT REMOVE THIS LABEL DISTRIBUTED BY LINDE, INC. DANBURY, CT 06810-6268

nitrous oxide

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Nitrous Oxide	ACTIVE INGREDIENT	K50XQU1029	2
Nitrous Oxide	ACTIVE MOIETY	K50XQU1029	2

Products#

Every source-derived product name is available through these pages.

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

NITROUS OXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59579-004	59579-004-01, 59579-004-02, 59579-004-03, 59579-004-04, 59579-004-05, 59579-004-06, 59579-004-07, 59579-004-08, 59579-004-09, 59579-004-10, 59579-004-11, 59579-004-12, 59579-004-15, 59579-004-16, 59579-004-17, 59579-004-18, 59579-004-19, 59579-004-20, 59579-004-13, 59579-004-14, 59579-004-21, 59579-004-22, 59579-004-23, 59579-004-24, 59579-004-25, 59579-004-26, 59579-004-27, 59579-004-28, 59579-004-29, 59579-004-30, 59579-004-31, 59579-004-32, 59579-004-33, 59579-004-34, 59579-004-35, 59579-004-36, 59579-004-37

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
Name	UNII	Kind
NITROUS OXIDE	K50XQU1029	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
11	2025-01-22	full-release	2026-05-31 21:24:00

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog.

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
NITROUS OXIDE	NITROUS OXIDE	Linde Gas & Equipment Inc.	b7e230d1-e201-4984-ba8b-5b88ec5a1bbf	2026-05-14		Exact identifier ndc (package): 59579-004-16 ndc (package): 59579-004-20 ndc (package): 59579-004-30 ndc (package): 59579-004-05 ndc (package): 59579-004-15 ndc (package): 59579-004-24 ndc (package): 59579-004-13 ndc (package): 59579-004-02 ndc (package): 59579-004-34 ndc (package): 59579-004-23 ndc (package): 59579-004-33 ndc (package): 59579-004-21 ndc (package): 59579-004-37 ndc (package): 59579-004-14 ndc (package): 59579-004-07 ndc (package): 59579-004-18 ndc (package): 59579-004-35 ndc (package): 59579-004-36 ndc (package): 59579-004-27 ndc (package): 59579-004-32 ndc (package): 59579-004-25 ndc (package): 59579-004-22 ndc (package): 59579-004-12 ndc (package): 59579-004-29 ndc (package): 59579-004-03 ndc (package): 59579-004-09 ndc (package): 59579-004-19 ndc (package): 59579-004-28 ndc (package): 59579-004-06 ndc (package): 59579-004-26 ndc (package): 59579-004-04 ndc (package): 59579-004-11 ndc (package): 59579-004-10 ndc (package): 59579-004-01 ndc (package): 59579-004-31 ndc (package): 59579-004-08 ndc (package): 59579-004-17 ndc (product): 59579-004 ndc11 (package): 59579000419 ndc11 (package): 59579000435 ndc11 (package): 59579000433 ndc11 (package): 59579000403 ndc11 (package): 59579000432 ndc11 (package): 59579000412 ndc11 (package): 59579000416 ndc11 (package): 59579000404 ndc11 (package): 59579000431 ndc11 (package): 59579000406 ndc11 (package): 59579000420 ndc11 (package): 59579000408 ndc11 (package): 59579000410 ndc11 (package): 59579000430 ndc11 (package): 59579000418 ndc11 (package): 59579000428 ndc11 (package): 59579000409 ndc11 (package): 59579000422 ndc11 (package): 59579000425 ndc11 (package): 59579000423 ndc11 (package): 59579000417 ndc11 (package): 59579000437 ndc11 (package): 59579000426 ndc11 (package): 59579000415 ndc11 (package): 59579000436 ndc11 (package): 59579000401 ndc11 (package): 59579000407 ndc11 (package): 59579000427 ndc11 (package): 59579000434 ndc11 (package): 59579000421 ndc11 (package): 59579000429 ndc11 (package): 59579000414 ndc11 (package): 59579000405 ndc11 (package): 59579000413 ndc11 (package): 59579000424 ndc11 (package): 59579000411 ndc11 (package): 59579000402 spl id: 41f0e138-c520-46da-b383-c96ad842016d spl set id: b7e230d1-e201-4984-ba8b-5b88ec5a1bbf

Reported adverse events (FAERS/openFDA)#

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