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  4. NDC Product Code: 62171-020 Uv Mild Sun Block

NDC 62171-020 Uv Mild Sun Block

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62171-020?
  4. Uv Mild Sun Block 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:
62171-020
Proprietary Name:
Uv Mild Sun Block
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Coson Co., Ltd.
Labeler Code:
62171
Product Label ID:
8ae9b5f1-050e-4a71-addd-0e578f797714
Start Marketing Date: [9]
03-01-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 62171-020?

The NDC code 62171-020 is assigned by the FDA to the product Uv Mild Sun Block which is product labeled by Coson Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62171-020-01 50 ml in 1 carton . 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 Uv Mild Sun Block?

Indication and Usage:At your final skin care step, apply it to your whole face with the proper amount after all your basic skin care.If you feel more perfect UV protect effect, apply it more whenever needed.

Which are Uv Mild Sun Block UNII Codes?

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

Which are Uv Mild Sun Block 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".