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  4. NDC Product Code: 21220-129 Carbon Dioxide Oxygen Mixture

NDC 21220-129 Carbon Dioxide Oxygen Mixture

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 21220-129?
  4. Active Ingredients UNII Codes
  5. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21220-129
Proprietary Name:
Carbon Dioxide Oxygen Mixture
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
General Air Service & Supply Co
Labeler Code:
21220
Product Label ID:
146d6c38-ae8c-4aa9-abeb-62005803e47a
Start Marketing Date: [9]
01-01-1975
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 21220-129?

The NDC code 21220-129 is assigned by the FDA to the product Carbon Dioxide Oxygen Mixture which is product labeled by General Air Service & Supply Co. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 21220-129-01 7101 l in 1 cylinder , 21220-129-02 707 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 Mixture UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Carbon Dioxide Oxygen Mixture?

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: 541999 - carbon dioxide 20 % / oxygen 80 % Gas for Inhalation

* Please review the disclaimer below.

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".