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  4. NDC Product Code: 12213-726 Carbon Dioxide/oxygen Mix

NDC 12213-726 Carbon Dioxide/oxygen Mix

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 12213-726?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
12213-726
Proprietary Name:
Carbon Dioxide/oxygen Mix
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nexair, Llc
Labeler Code:
12213
Product Label ID:
74cf86ac-9c48-4ecc-a3aa-ba0a03de4f70
Start Marketing Date: [9]
06-01-1996
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 12213-726?

The NDC code 12213-726 is assigned by the FDA to the product Carbon Dioxide/oxygen Mix which is product labeled by Nexair, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 12213-726-14 6400 l in 1 cylinder , 12213-726-58 708 l in 1 cylinder . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

Which are Carbon Dioxide/oxygen Mix UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Carbon Dioxide/oxygen Mix Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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] 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".