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  4. NDC Product Code: 43695-0005 Zeta Clear

NDC 43695-0005 Zeta Clear

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43695-0005?
  4. Zeta Clear 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:
43695-0005
Proprietary Name:
Zeta Clear
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pacific Naturals
Labeler Code:
43695
Product Label ID:
e6c8e24b-92ea-4fe4-968e-2ab221e55dea
Start Marketing Date: [9]
04-25-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 43695-0005?

The NDC code 43695-0005 is assigned by the FDA to the product Zeta Clear which is product labeled by Pacific Naturals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43695-0005-1 30 ml in 1 bottle, spray . 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 Zeta Clear?

Treats the symptoms of funal infections of the toenail such as toenails that are: discolored; brittle, crumbly or ragged; separated from the nail bed; and or painful.  Treats the symptoms of funal infections of the toenail such as toenails that are: discolored; brittle, crumbly or ragged; separated from the nail bed; and or painful.

Which are Zeta Clear UNII Codes?

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

Which are Zeta Clear 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".