NDC 60207-001 Oxygen

Product Information

Product Code	60207-001
Proprietary Name What is the Proprietary Name? The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.	Oxygen
Product Labeler Information What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.	Apple Homecare Associates, Inc.
Labeler Code	60207
Start Marketing Date What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.	01-01-1990
Listing Expiration Date What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.	12-31-2017
Exclude Flag What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".	I
NDC Code Structure	60207 - Apple Homecare Associates, Inc. 60207-001 - Oxygen 60207-001-01 60207-001-02

Product Packages

NDC 60207-001-02

Package Description: 41 L in 1 DEWAR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Oxygen is product labeled by Apple Homecare Associates, Inc.. The product's dosage form is and is administered via form.

What are Oxygen Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

OXYGEN (UNII: S88TT14065)
OXYGEN (UNII: S88TT14065) (Active Moiety)

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

RxCUI: 312172

* Please review the disclaimer below.

Oxygen Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

OXYGEN REFRIGERATED LIQUID USP LABEL

Oxygen Refrigerated Liquid Usp Label

OXYGEN REFRIGERATED LIQUID USP UN1073 CONTENTS_________ LITERS ALWAYS KEEP CONTAINER IN UPRIGHT POSITION. WARNING: DO NOT CHANGE OR FORCE FIT CONNECTIONS. EXTREMELY COLD LIQUID AND GAS UNDER PRESSURE. VIGOROUSLY ACCELERATES COMBUSTION. NO SMOKING IN THE PRESENCE OF OXYGEN OR A FIRE MAY RESULT. COMBUSTIBLES IN CONTACT WITH LIQUID OXYGEN MAY EXPLODE ON IGNITION OR IMPACT. CAN CAUSE SEVERE FROSTBITE. KEEP OIL, GREASE AND COMBUSTIBLES AWAY. USE ONLY WITH EQUIPMENT CLEANED FOR OXYGEN SERVICE. STORE AND USE WITH ADEQUATE VENTILATION. DO NOT GET LIQUID IN EYES, ON SKIN OR CLOTHING. FOR LIQUID WITHDRAWAL, WEAR FACE SHIELD AND GLOVES. DO NOT DROP. USE SUITABLE HAND TRUCK FOR CONTAINER MOVEMENT. AVOID SPILLS. DO NOT WALK OR ROLL EQUIPMENT OVER SPILLS CONTAINER TEMPERATURE SHOULD NOT EXCEED 52C (125 F) CLOSE VALVE AFTER EACH USE AND WHEN EMPTY. USE A BACK FLOW PREVENTATIVE DEVICE IN THE PIPING. USE IN ACCORDANCE WITH THE MATERIAL SAFETY DATA SHEET (MSDS)

FIRST AID: IN CASE OF FROSTBITE OBTAIN MEDICAL TREATMENT IMMEDIATELY.

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. USE ONLY WITH PRESSURE REDUCING EQUIPMENT AND APPARATUS DESIGNED FOR OXYGEN. DO NOT ATTEMPT TO USE ON PATIENTS WHO HAVE STOPPED BREATHING, UNLESS USED IN CONJUNCTION WITH RESUSCITATIVE EQUIPMENT. PRODUCED BY AIR LIQUEFACTION. DO NOT REMOVE THIS PRODUCT LABEL.

OXYGEN USP LIQUID LABEL - apple hc liq o2