FDA.reportPublic FDA data

FDA label 670ca6ff-5237-4e6f-b33a-31957a29bf25

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
181da877-f77a-4d68-9055-80c9f2bf6b59
SPL ID
670ca6ff-5237-4e6f-b33a-31957a29bf25
Version
1
Effective date
2010-01-01
Source export date
2026-08-01
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5cbbf4af8f4e275ec50931155b30ffa7322568b9af8a1c936a47f6d6774862fd/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:03:03

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 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 SHEET AND SAFETY PROCEDURES RECOMMENDED BY THE SUPPLIER. WARNING: FEDERAL LAW PROHIBITS DISPENSING THIS PRODUCT WITHOUT A PRESCRIPTION. PRODUCED BY AIR LIQUEFACTION. DO NOT REMOVE THIS PRODUCT LABEL.