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  4. NDC Product Code: 66078-503 Sun Total Protector Color 30 Light Tint

NDC 66078-503 Sun Total Protector Color 30 Light Tint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66078-503?
  4. Sun Total Protector Color 30 Light Tint Uses
  5. 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:
66078-503
Proprietary Name:
Sun Total Protector Color 30 Light Tint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Md Formulations
Labeler Code:
66078
Product Label ID:
e3956a48-4055-4520-a0c3-c54d36df84e0
Start Marketing Date: [9]
05-20-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 66078-503?

The NDC code 66078-503 is assigned by the FDA to the product Sun Total Protector Color 30 Light Tint which is product labeled by Md Formulations. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66078-503-25 42 carton in 1 case / 1 bottle in 1 carton / 75 ml in 1 bottle. 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 Sun Total Protector Color 30 Light Tint?

Uses to help prevent sunburn and for the temporary protection of sunburn.

Which are Sun Total Protector Color 30 Light Tint 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".