{"effective_time":"20111213","id":"bc96af44-7ddd-0481-bfed-90f4ad83af5c","openfda":{},"package_label_principal_display_panel":["PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Helium USP Certificate of Analysis Product: Helium, USP Date Facility Name Facility Address Lot # Batch # Final Analysis Results Analyzer # Test / Units USP Specs Analysis Results GC 1 % Helium Assay > 99.0% % GC 1 % Air < 1.0% ppm N2 ppm O2 Drager Tube ppm CO < 10 ppm ppm N/A Odor None N/A Identification Pass NT = not tested The methodology used to perform the assay and air USP tests : 1 The assay and air determinations are performed using a Gow-Mac Gas Chromatograph Manufacturer Model: #590-1 or a Valco Gas Chromatograph Manufacturer Model: #5000 Analyst Date Quality Reviewer Date Should the material not be delivered to a USP customer, the material is “Not Approved for Human Drug Use.” July 2010 Helium USP Certificate of Analysis Page 1 of 1 Copyright © The Linde Group – Distributed by a locally registered Linde company"],"package_label_principal_display_panel_table":["
Product: Helium, USP
Date
Facility Name
Facility Address
Lot # Batch #
","
Analyzer # Test / Units USP Specs Analysis Results
GC1 % Helium Assay > 99.0% %
GC1 % Air < 1.0% ppm N2 ppm O2
Drager Tube ppm CO < 10 ppm ppm
N/A Odor None
N/A Identification Pass
","
Analyst Date
","
Quality Reviewer Date
"],"set_id":"416a803e-5d87-2dc6-a98f-625587ede004","spl_product_data_elements":["Helium Helium Helium Helium label"],"version":"2"}