AIR COMPRESSED by O.E. Meyer Company / O.E. Meyer Co. AIR COMPRESSED gas

AIR COMPRESSED by

Drug Labeling and Warnings

AIR COMPRESSED by is a Prescription medication manufactured, distributed, or labeled by O.E. Meyer Company, O.E. Meyer Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AIR, COMPRESSED LABEL

AIR, COMPRESSED USP UN1002 NON-FLAMMABLE GAS 2 37338 (01/15)

MEDICAL AIR

WARNING: For breathing support when used by properly trained personnel. For medical applications. Rx only. Administration of Medical Air 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 Medical Air 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: CONTAINS GAS UNDER PRESSURE; MAY EXPLODE IF HEATED, SUPPORTS COMBUSION.  Do not handle until all safety precautions have been read and understood. Use a backflow preventive device I the piping. Use only with equipment of compatible materials of construction and rated for cylinder pressure. Close valve after each use and when empty. Protect from sunlight when ambient temperature exceeds 52°C (125°F). Read and follow the Safety Data Sheet (SDS) before use.

CAS 132259-10-0               DO NOT REMOVE THIS PRODUCT LABEL.

CONTENTS:         LTRS.      _______

                                CU. FT. _______

O.E. MEYER COMPANY

3303 TIFFIN AVE. SANDUSKY, OH 44870

419-6253054

INGREDIENTS AND APPEARANCE

AIR COMPRESSED 
air compressed gas

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 47632-0025
Route of Administration	RESPIRATORY (INHALATION)

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYGEN (UNII: S88TT14065) (OXYGEN - UNII:S88TT14065)	OXYGEN	20 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
NITROGEN (UNII: N762921K75)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47632-0025-1	5900 L in 1 CYLINDER; Type 0: Not a Combination Product	12/15/1988
2	NDC: 47632-0025-2	730 L in 1 CYLINDER; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	12/15/1988

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA205765	12/15/1988

Labeler - O.E. Meyer Company (555452523)

Registrant - O.E. Meyer Company (555452523)

Establishment
Name	Address	ID/FEI	Business Operations
O.E. Meyer Company		555452523	manufacture(47632-0025)