Oxygen
FDA Label NDC 68698-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Oxygen Plus Llc for the product Oxygen (NDC 68698-001). 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 refrigerated liquid label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Oxygen Refrigerated Liquid Label

OXYGEN REFRIGERATED LIQUID UN 1073  OXYGEN-2  ALWAYS KEEP CONTAINER IN UPRIGHT POSITION  WARNING: EXTREMELY COLD OXIDIZING LIQUID AND GAS UNDER PRESSURE  VIGOROUSLY ACCELERATES COMBUSTION  COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT.  CAN CAUSE SEVERE FROSTBITE.  KEEP OIL GREASE AND COMBUSTIBLES AWAY.  USE ONLY WITH EQUIPMENT CLEANED FOR OXYGEN SERVICE STORE AND USE WITH ADEQUATE VENTILATION  DO NOT GET LIQUID IN EYES, ON SKIN OR CLOTHING  FOR LIQUID WITHDRAWAL, WEAR FACE SHIELD AND GLOVES  DO NOT DROP  USE HAND TRUCK FOR CONTAINER MOVEMENT.  AVOID SPILLS  DO NOT WALK ON OR ROLL EQUIPMENT OVER SPILLS.  CLOSE VALVE AFTER EACH USE AND WHEN EMPTY.  USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS)  FIRST AID: IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY.  DO NOT REMOVE THIS PRODUCT LABEL.   CAS 7782-44-7

Liquid Label (Oxygen Plus Liq O2)

Liquid Label (Oxygen Plus Liq O2)

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