Label: OXYGEN gas
- NDC Code(s): 74911-001-01, 74911-001-02, 74911-001-03, 74911-001-04
- Packager: Ogles Oxygen, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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 December 27, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Principal for Oxygen Product
Oxygen, Compressed
USP UN1072
Produced by Air Liquefaction
Do Not Remove
This Product Label.
Danger: May cause or intensify fire; oxidizer.
Contains gas under pressure; may explode if heated.
Warning: For emergency use only when administered by properly trained personnel for oxygen
deficiency and resuscitation. For all other medical applications. Rx Only. Uninterrupted use of high
concentrations of oxygen over a long duration, without monitoring its effect on oxygen content of
arterial blood, may be harmful. Do not attempt to use on patients who have stopped breathing
unless used in conjunction with resuscitative equipment. Keep out of reach of children. Federal law
requires that this container by refilled with oxygen USP only by established registered as a drug
manufacturer in accordance with the federal Food, Drug and Cosmetic Act.
Danger: Do not handle until all safety precautions have been read and understood. Keep and
store away from clothing and other combustible materials. Keep valves and fittings free from
grease and oil. Use and store only outdoors or in a well-ventilated place. In case of fire: Stop leak
if safe to do so. Use a back flow preventive device in the piping. Use only with equipment cleaned
for oxygen service. Open valve slowly. Close valve after each use and when empty. Protect from
sunlight when ambient temperature exceeds 52ºC(125ºF) Read and follow the Safety Data Sheet
(SDS) before use.
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INGREDIENTS AND APPEARANCE
OXYGEN
oxygen gasProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:74911-001 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYGEN (UNII: S88TT14065) (OXYGEN - UNII:S88TT14065) OXYGEN 99 L in 100 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74911-001-01 165 L in 1 CYLINDER; Type 0: Not a Combination Product 04/07/2020 2 NDC:74911-001-02 359 L in 1 CYLINDER; Type 0: Not a Combination Product 04/07/2020 3 NDC:74911-001-03 655 L in 1 CYLINDER; Type 0: Not a Combination Product 04/07/2020 4 NDC:74911-001-04 1699 L in 1 CYLINDER; Type 0: Not a Combination Product 04/07/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved medical gas 04/07/2020 Labeler - Ogles Oxygen, LLC (079708390) Establishment Name Address ID/FEI Business Operations Ogles Oxygen, LLC 079708390 manufacture(74911-001)