Oxygen
FDA Label NDC 67378-001
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by B-pharm, Inc Dba Remedies Medical Equipment for the product Oxygen (NDC 67378-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding oxygen compressed label, warnings and precautions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings And Precautions
OXYGEN COMPRESSED USP
UN1072 OXYGEN 2
WARNING: For emergency use only when administered by properly trained personnel for Oxygen deficiency and resuscitation. For all other medical applications Rx Only. Uninterrupted use of high
concentrations of Oxygen over a long duration, without monitoring its effect on oxyen 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.
PRODUCED BY AIR LIQUEFACTION.
Warning: HIGH PRESSURE OXIDIZING GAS. VIGOROUSLY ACCELERATED COMBUSTION. Keep oil and grease away. Open valve slowly. Store and use with adequate ventilation. Use only with equipment cleaned for Oxygen Service and rated for cylinder pressure. Use a back flow preventative device in piping. Close valve after each use and when empty. Cylinder temperature should not exceed 52 C (125 F) Use in accordance with the Material Safety Data Sheet (MSDS) CAS 7782-44-7 Do Not Remove this Product Label
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