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  4. NDC Product Code: 60681-0401 Pleo Art U

NDC 60681-0401 Pleo Art U

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60681-0401?
  4. Pleo Art U Uses
  5. Active Ingredients UNII Codes
  6. 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:
60681-0401
Proprietary Name:
Pleo Art U
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sanum Kehlbeck Gmbh & Co. Kg
Labeler Code:
60681
Product Label ID:
be9343ef-d1cf-491c-ab18-cb1431d9bbf1
Start Marketing Date: [9]
02-19-1997
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 60681-0401?

The NDC code 60681-0401 is assigned by the FDA to the product Pleo Art U which is product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60681-0401-1 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper. 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.

What are the uses for Pleo Art U?

This product is used as To temporarily restore mental alertness during periods of fatigue

Which are Pleo Art U UNII Codes?

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

  • BREVIBACTERIUM STATIONIS (UNII: 118V62TZ38)
  • BREVIBACTERIUM STATIONIS (UNII: 118V62TZ38) (Active Moiety)

Which are Pleo Art U 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".