MESSER Gases for Life Bulk Carbon Dioxide USP Certificate of Analysis This is to certify that the carbon dioxide tested at MESSER PLANT on 10/27/2025, meets the United States Pharmacopoeia (USP) specifications, the requirements of Federal Specifications BB-C-101 Grade A and QVL E of CGA G6.2. This product was manufactured at a facility registered with the Federal Food and Drug Administration and is approved for prescription drug use. This product is not guaranteed to meet any other specification or intended for pesticide use. NDA 205764 NADA 141362 Furthermore, batch number 5784-A-102725-01, and lot number TCO2002-102725-13, which was loaded on 10/27/2025 and produced at MESSER PLANT comprises this shipment and was analyzed as shown below. Analytical results are generated using USP monograph or validated equivalent methods. FOR MEDICAL USE Requirement Analytical Method Limit of Detection Specification Limit Result Carbon Dioxide Assay (CO2) Speed of Sound 99.99 % 99.0 % 99.99% Nitrogen Oxide (NO) IMR-MS 0.05 ppm 2.5 ppm ND Nitrogen Dioxide (NO2) IMR-MS 0.1 ppm 2.5 ppm ND Ammonia (NH3) IMR-MS 0.03 ppm 25 ppm ND Sulfur Dioxide (SO2) IMR-MS 0.03 ppm 5 ppm ND Hydrogen Sulfide (H2S) IMR-MS 0.03 ppm 1 ppm ND Carbon Monoxide (CO) FTIR 0.05 ppm 10 ppm ND Moisture (H2O) Quartz Crystal 0.5 ppm 200 ppm 0.77 ppm Notes: 1. Positive Carbon Dioxide Identification is achieved when the Assay results demonstrate meeting the specification. 2. The limit of detection (LOD) for each test method is the threshold value for results to be reported with certainty in the accuracy of results. A test result outside the detection limit for the test method will be reported as ND. 3. ND = None Detected 4. ppm = parts per million by volume, ppb = parts per billion by volume, 1 ppm = 1,000 ppb Product analyzed using Messer Ultra Guard Suite Certified By: (Signature) (Date) John Doe (Print Name & Title) On behalf of Messermesser llc carbon dioxide coa 2025
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
