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  4. NDC Product Code: 62908-013 Noevir 5 Treatment Liquid Foundation Lx

NDC 62908-013 Noevir 5 Treatment Liquid Foundation Lx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62908-013?
  4. Active 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:
62908-013
Proprietary Name:
Noevir 5 Treatment Liquid Foundation Lx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Noevir Usa Inc
Labeler Code:
62908
Product Label ID:
cc17ad55-ae6a-4827-869a-923a7fd3deda
Start Marketing Date: [9]
08-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62908-013?

The NDC code 62908-013 is assigned by the FDA to the product Noevir 5 Treatment Liquid Foundation Lx which is product labeled by Noevir Usa Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62908-013-02 1 tube in 1 box / 38 g in 1 tube (62908-013-01). 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 Noevir 5 Treatment Liquid Foundation Lx UNII Codes?

The UNII codes for the active 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".