Label: OXYGEN gas
-
Contains inactivated NDC Code(s)
NDC Code(s): 52428-001-01, 52428-001-02, 52428-001-03, 52428-001-04, view more52428-001-05 - Packager: Arkansas Home Medical
- Category: HUMAN PRESCRIPTION DRUG LABEL
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 9, 2013
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
OXYGEN REFRIGERATED LIQUID LABEL
OXYGEN REFRIGERATED LIQUID USP UN 1073 OXYGEN-2 CAS 7782-44-7 ALWAYS KEEP CONTAINER IN UPRIGHT POSITION CONTENTS___________________ DO NOT CHANGE OR FORCE FIT CONNECTIONS. 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 OXYGEN CONCENTRATION 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: 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 SUITABLE HAND TRUCK FOR CONTAINER MOVEMENT. AVOID SPILLS. DO NOT WALK ON OR ROLL EQUIPMENT OVER SPILLS. CONTAINER TEMPERATURE SHOULD NOT EXCEED 52C (125 F) CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING. USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS) FIRST AID: IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY. DO NOT REMOVE THIS LABEL.
-
INGREDIENTS AND APPEARANCE
OXYGEN
oxygen gasProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52428-001 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYGEN (UNII: S88TT14065) (OXYGEN - UNII:S88TT14065) OXYGEN 99 L in 100 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52428-001-01 21 L in 1 DEWAR 2 NDC:52428-001-02 31 L in 1 DEWAR 3 NDC:52428-001-03 36 L in 1 DEWAR 4 NDC:52428-001-04 41 L in 1 DEWAR 5 NDC:52428-001-05 45 L in 1 DEWAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved medical gas 06/16/2010 Labeler - Arkansas Home Medical (147884998) Registrant - Arkansas Home Medical (147884998) Establishment Name Address ID/FEI Business Operations Arkansas Home Medical 147884998 manufacture(52428-001) Establishment Name Address ID/FEI Business Operations Arkansas Home Medical 167840136 manufacture(52428-001)