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  4. NDC Product Code: 69570-102 Hand And Skin Shield

NDC 69570-102 Hand And Skin Shield

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69570-102?
  4. Hand And Skin Shield 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:
69570-102
Proprietary Name:
Hand And Skin Shield
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dcg Vision Marketing & Sales International Ltd.
Labeler Code:
69570
Product Label ID:
b73eb24f-6c6c-4ea9-ae6c-c0fe5547e9cd
Start Marketing Date: [9]
04-08-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 69570-102?

The NDC code 69570-102 is assigned by the FDA to the product Hand And Skin Shield which is product labeled by Dcg Vision Marketing & Sales International Ltd.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 69570-102-11 502 ml in 1 bottle , 69570-102-12 100 ml in 1 bottle , 69570-102-13 100 ml 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 Hand And Skin Shield?

• Clean and dry hands and skin. Apply True Effects Hand & Skin Shield™ to the palm of hand and rub thoroughly into hands and skin, making sure front and back of hands including cuticles are completely covered. Allow to dry for 3-5 minutes or until completely absorbed into skin. • After coming into contact with dangerous chemicals, wash hands thoroughly and reapply.

Which are Hand And Skin Shield UNII Codes?

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

Which are Hand And Skin Shield 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".