Nitrogen Gas
FDA Label NDC 64922-240

NITROGEN REFRIGERATED LIQUID NF UN 1977 NON-FLAMMABLE GAS  CONTENTS ________________ LOT NUMBER ________________  ALWAYS KEEP CONTAINER IN UPRIGHT POSITION  DO NOT REMOVE THIS PRODUCT LABEL  WARNING Rx ONLY.  PLEASE REFER TO THE MATERIAL SAFETY DATA SHEET FOR SAFETY AND PRODUCT INFORMATION

IF INHALED, REMOVE TO FRESH AIR.  IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION.  IF BREATHING IS DIFFICULT, GIVE OXYGEN.  CALL A PHYSICIAN.  IN CASE OF FROSTBITE, OBTAIN MEDICAL TREATMENT IMMEDIATELY.

PART # DB-NNF PRINTED BY RATERMANN MFG INC.  925-606-2949

Liquid Nitrogen Label (Adf Large Lq N2)

NITROGEN COMPRESSED NF UN 1066 NON-FLAMMABLE GAS - 2 DO NOT REMOVE THIS PRODUCT LABEL

CONTENTS ________ PRESSURE ____________ CAUTION: HIGH PRESSURE GAS CAN CAUSE RAPID SUFFOCATION.  STORE AND USE WITH ADEQUATE VENTILATION.  USER SHALL SECURE CYLINDER IN USE AND IN STORAGE.  USE IN UPRIGHT POSITION.  USE ONLY WITH EQUIPMENT DESIGNATED FOR NITROGEN SERVICE AND RATED FOR CYLINDER PRESSURE.  CLOSE VALVE AFTER EACH USE.  KEEP VALVE PROTECTIVE CAP IN PLACE WHEN NOT IN USE IF SO EQUIPPED.  USE IN ACCORDANCE WITH MSDS.  CAUTION: FEDERAL LAW PROHIBITS DISPENSING WITHOUT PRESCRIPTION.  WARNING: ADMINISTRATION OF NITROGEN MAY BE HAZARDOUS OR CONTRAINDICATED.  FOR USE ONLY BY OR UNDER THE SUPERVISION OF A LICENSED PRACTITIONER WHO IS EXPERIENCED IN THE USE AND ADMINISTRATION OF NITROGEN AND IS FAMILIAR WITH THE INDICATIONS, EFFECTS, DOSAGES, METHODS, AND FREQUENCY AND DURATION OF ADMINISTRATION, AND WITH THE HAZARDS, CONTRAINDICATIONS AND SIDE EFFECTS AND THE PRECAUTIONS TO BE TAKEN.  FIRST AID: IF INHALED REMOVE TO FRESH AIR.  IF NOT BREATHING, GIVE ARTIFICIAL RESPIRATION.  IF BREATHING IS DIFFICULT GIVE OXYGEN, CALL A PHYSICIAN.  CAS 7727-37-9 RETURN WITH 25 PSIG.  LABEL 14

Nitrogen Shoulder Label (Adfws Hp N2)

               CUSTOMER ___________________  VENDOR / SUPPLIER ________________________  THIS LETTER IS TO PROVIDE YOU WITH THE
               CERTIFICATION YOU REQUESTED FOR NITROGEN NF LOT NUMBER _______________________ SUPPLIED TO YOU IN
               CYLINDERS / VESSELS BY OUR LOCATION

               These cylinders were filled in accordance with the Standard Operating Procedures utilized for the manufacture of Medical Gases.  By
               following these procedures, our location ensures that products are safely manufactured in compliance with FDA’s Current Good Manufacturing Practices
               (cGMP) Regulations. 
               CAUTION: VENDOR SUPPLIES THIS CERTIFICATION TO CUSTOMER TO ASSIST CUSTOMER IN ENSURING COMPLIANCE WITH 21 CFR 211.84.  THIS
               CERTIFICATION DOES NOT ELIMINATE CUSTOMERS OBLIGATION TO COMPLY WITH OTHER PORTIONS OF 21 CFR 210 AND 211, INCLUDING BUT NOT
               LIMITED TO 21 CFR 211.165 (FINISHED PRODUCT TESTING) FOR CYLINDERS AND VESSELS FILLED FROM THESE SUPPLY CYLINDERS.  THESE CYLINDERS ARE
               NOT CERTIFIED FOR INSTRUMENT CALIBRATION.

TEST REQUIREMENT           USP SPECIFICATION                  LOT ANALYSIS
IDENTIFICATION                         PASS
ODOR                                        PASS
CARBON DIOXIDE                    LESS THAN 1.0%
CARBON MONOXIDE                LESS THAT 10 PPM
ASSAY                                     GREATER THAN 99.0%



The methodology being used to perform the NF Test for
               Assay is indicated below:   Paramagnetic Analyzer    Model # ________________________ ELECTROCHEMICAL ANALYZER MODEL #________________ GAS CHROMATOGRAPHY OFFICIAL USP / NF METHOD