HELIUM - helium gas 
Linde LLC

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

 

 

label

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

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

 

NT = not tested The methodology used to perform the assay and air USP tests:1The 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

 


HELIUM  
helium gas
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52438-015
Route of AdministrationRESPIRATORY (INHALATION)DEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Helium (Helium) Helium990 mL  in 1 L
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMultilevel Packaging
1NDC:52438-015-2041635 L in 1 TANKNone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved medical gas08/26/196512/15/2011

Labeler - Linde LLC (001368141)

Revised: 12/2011 Linde LLC