FDA label 028d48ef-033d-49dc-8469-cde41d66ccf2

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
fcadac08-30d0-46c2-9053-af28481b86a3
SPL ID
028d48ef-033d-49dc-8469-cde41d66ccf2
Version
1
Effective date
2010-01-01
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:42:08

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings and cautions

PRODUCT WARNINGS AND PRECAUTIONS WARNING: SECURE ALL CYLINDERS WHILE IN STORAGE AND IN USE. UNINTERRUPTED USE OF HIGH CONCENTRATIONS OF OXYGEN OVER A LONG DURATION WITHOUT MONITORING ITS EFFECT ON OXYGEN CONTENT OF ARTERIAL BLOOD MAY BE HARMFUL. USE ONLY WITH PRESSURE REDUCING EQUIPMENT AND APPARATUS DESIGNED FOR OXYGEN. DO NOT ATTEMPT TO USE ON PATIENTS WHO HAVE STOPPED BREATHING, UNLESS USED IN CONJUNCTION WITH RESUSCITATIVE EQUIPMENT. USE IN ACCORDANCE WITH MATERIAL SAFETY DATA SHEETS AND SAFETY PRECAUTIONS RECOMMENDED BY THE SUPPLIER. WARNING: FEDERAL LAW PROHIBITS DISPENSING WITHOUT A PRESCRIPTION. PRODUCED BY AIR LIQUEFACTION. DO NOT REMOVE THIS PRODUCT LABEL.

Reported adverse events (FAERS/openFDA)#

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