1. Home
  2. Labeler Index
  3. Coson Co., Ltd.
  4. NDC Product Code: 62171-010 Dr Myers Water Keep Skins

NDC 62171-010 Dr Myers Water Keep Skins

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62171-010?
  4. Dr Myers Water Keep Skins 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:
62171-010
Proprietary Name:
Dr Myers Water Keep Skins
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Coson Co., Ltd.
Labeler Code:
62171
Product Label ID:
bae9b2e0-a435-4343-91e7-d6fb6df11bd1
Start Marketing Date: [9]
01-02-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 62171-010?

The NDC code 62171-010 is assigned by the FDA to the product Dr Myers Water Keep Skins 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 62171-010-01 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 Dr Myers Water Keep Skins?

INDICATIONS AND USAGE:In the last step of skin care, spread it softly on the whole face.Beside the face, you can use it on any area if you think sunscreen needed.

Which are Dr Myers Water Keep Skins UNII Codes?

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

Which are Dr Myers Water Keep Skins 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:

* Please review the disclaimer below.

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".