NDC 58420-006 Carbon Dioxide

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
Proprietary Name:
Carbon Dioxide
Product Type: [3]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

Code Structure Chart

Product Details

What is NDC 58420-006?

The NDC code 58420-006 is assigned by the FDA to the product Carbon Dioxide which is product labeled by Airgas Intermountain Inc. The product's dosage form is . The product is distributed in 13 packages with assigned NDC codes 58420-006-01 169 l in 1 cylinder , 58420-006-02 183 l in 1 cylinder , 58420-006-03 196 l in 1 cylinder , 58420-006-04 594 l in 1 cylinder , 58420-006-05 934 l in 1 cylinder , 58420-006-06 1217 l in 1 cylinder , 58420-006-07 1585 l in 1 cylinder , 58420-006-08 2462 l in 1 cylinder , 58420-006-09 3707 l in 1 cylinder , 58420-006-10 4953 l in 1 cylinder , 58420-006-11 6169 l in 1 cylinder , 58420-006-12 7415 l in 1 cylinder , 58420-006-13 12367 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 UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Carbon Dioxide?

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:

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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".