Label: LIQUID OXYGEN gas

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved medical gas

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 September 28, 2009

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  • PRINCIPAL DISPLAY PANEL

    Oxygen, Refrigerated Liquid USP
    UN1073

    Produced by air liquefaction

    CAUTION: Federal Law Prohibits dispensing without prescription

    This Unit when full contains __ Liquid Liters.

    Principal Display Panel for Liquid Oxygen
  • INGREDIENTS AND APPEARANCE
    LIQUID OXYGEN 
    liquid oxygen gas
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65360-1073
    Route of AdministrationRESPIRATORY (INHALATION)
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYGEN (UNII: S88TT14065) (OXYGEN - UNII:S88TT14065) OXYGEN995 mL  in 1 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65360-1073-121 L in 1 CYLINDER
    2NDC:65360-1073-231 L in 1 CYLINDER
    3NDC:65360-1073-336 L in 1 CYLINDER
    4NDC:65360-1073-441 L in 1 CYLINDER
    5NDC:65360-1073-546 L in 1 CYLINDER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved medical gas01/02/1999
    Labeler - Community Home Health Services (072068141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Linde Gas North America LLC004174819manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Community Home Health Services072068141repack