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  4. NDC Product Code: 66078-504 Total Protector Color 30 Medium Tint

NDC 66078-504 Total Protector Color 30 Medium Tint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66078-504?
  4. Total Protector Color 30 Medium Tint 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:
66078-504
Proprietary Name:
Total Protector Color 30 Medium Tint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Md Formulation
Labeler Code:
66078
Product Label ID:
b18dc7a1-a9e7-4f35-a557-d7062613c1e4
Start Marketing Date: [9]
01-28-2005
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 66078-504?

The NDC code 66078-504 is assigned by the FDA to the product Total Protector Color 30 Medium Tint which is product labeled by Md Formulation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66078-504-25 42 carton in 1 case / 1 tube in 1 carton / 81 g in 1 tube. 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 Total Protector Color 30 Medium Tint?

When using this product do not use in or near the eyes. If product gets into eyes, rinse thoroughly with water.

Which are Total Protector Color 30 Medium Tint UNII Codes?

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

Which are Total Protector Color 30 Medium Tint 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".