FDA.reportPublic FDA data

Nitrous Oxide

Manufacturer
Linde Gas & Equipment Inc.
Effective date
2021-12-14
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 22:20:55

Label at a glance#

ProductNitrous Oxide
Active ingredientNitrous Oxide
Label structure2 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

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.

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 fittings 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 preventive 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 on 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.
WARNING: This product can expose you to nitrous oxide, which is known to the State of California to cause birth defects or other reproductive harm. For more information, go to www.P65Warnings.ca.gov.

DO NOT REMOVE THIS PRODUCT LABEL.

CONTENTS:
CYLINDER TYPELITERS
      160L  [_] 88737
      180L  [_] 96871
      200L  [_]105006
      230L  [_]123492
      ____________

Distributed by:
Linde Gas North America LLC
200 Somerset Corporate Blvd., Suite 7000
Bridgewater, NJ 08807
866.543.3427

LG041G 8/18
 

      

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

N2O USP Liquid Label 8-2018
N2O USP Liquid Label 8-2018

Linde
NITROUS OXIDE, REFRIGERATED LIQUID USP

UN2201
MEDICAL GAS
CAS: 10024-97-2

2

5.1

WARNING: USE OF ADAPTORS IS PROHIBITED

WARNING: DO NOT REMOVE FITTINGS

Rx only

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
25373-103-052025-12-18C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-062025-12-18C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-072025-12-18C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-082025-12-18C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-052023-01-30C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-062023-01-30C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-072023-01-30C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID
25373-103-082023-01-30C16284748780-1f386c64a-33b7-0266-e053-dadaa90a7c1aNITROUS OXIDE, REFRIGERATED LIQUID

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
25373-103NITROUS OXIDE (NITROUS OXIDE) GAS [LINDE GAS & EQUIPMENT INC.]8Legacy NDC20211225_77737bbb-80d5-2858-011d-08b028af6f27.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Nitrous OxideACTIVE INGREDIENTK50XQU10292
Nitrous OxideACTIVE MOIETYK50XQU10292

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
25373-10325373-103-05, 25373-103-06, 25373-103-07, 25373-103-08

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
41b07520-534c-45c0-bdb8-61e4d779cae777737bbb-80d5-2858-011d-08b028af6f272025-12-18WarningsExact identifier
spl set id: 77737bbb-80d5-2858-011d-08b028af6f27

Reported adverse events (FAERS/openFDA)#

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