Label: NITROGEN gas
- NDC Code(s): 65919-002-01
- Packager: Clinical 1 Home Medical, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Updated October 1, 2021
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Nitrogen Liquid Label
NITROGEN, REFRIGERATED LIQUID NF UN1977 NON-FLAMMABLE GAS 2
ALWAYS KEEP CONTAINER IN UPRIGHT POSITION
DO NOT CHANGE OR FORCE FIT CONNECTIONS.
RX ONLY LTRS:
CONTENTS:________________________________ CU FT:
WARNING: Administration of Nitrogen may be hazardous or contraindicated. For use only by or under the supervision of a licensed practitioner who is experienced in the use and administration of nitrogen and is familiar with the indications, effects, dosages, methods, and frequency and duration of administration, and with the hazards, contraindications and side effects and the precautions to be taken.
WARNING: EXTREMELY COLD LIQUID AND GAS UNDER PRESSURE.
CAN CAUSE RAPID SUFFOCATION.
CAN CAUSE SEVERE FROSTBITE.
Store and use with adequate ventilation.
Do not get liquid in eyes, on skin or clothing.
For liquid withdraw, wear face shield and gloves.
Do not drop. Use suitale hand truck for container movement.
Container temperature should not exceed 52 degrees C ( 125 degrees F).
Close valve after each use and when empty.
Use a back flow preventive device in the piping.
Use in accordance with the Material Safety Data Sheet (MSDS).
FIRST AID: IF INHALED, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen.
Call a physician.
IN CASE OF FROSTBITE, obtain medical treatment immediately.
DO NOT REMOVE THIS PRODUCT LABEL
INGREDIENTS AND APPEARANCE
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:65919-002 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NITROGEN (UNII: N762921K75) (NITROGEN - UNII:N762921K75) NITROGEN 99 L in 100 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65919-002-01 10 L in 1 DEWAR; Type 0: Not a Combination Product 06/01/2000 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA205839 06/01/2000 Labeler - Clinical 1 Home Medical, Inc. (110832404) Registrant - Clinical 1 Home Medical, Inc. (110832404) Establishment Name Address ID/FEI Business Operations Clinical 1 Home Medical, Inc. 110832404 manufacture(65919-002)