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  4. NDC Product Code: 65342-1392 Tinted Moisturizer Spf-20 Mocha

NDC 65342-1392 Tinted Moisturizer Spf-20 Mocha

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65342-1392?
  4. Tinted Moisturizer Spf-20 Mocha 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:
65342-1392
Proprietary Name:
Tinted Moisturizer Spf-20 Mocha
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gurwitch Products, L.l.c.
Labeler Code:
65342
Product Label ID:
ce3d8fa7-56bb-40bb-ae05-e5bb687ddf7d
Start Marketing Date: [9]
11-29-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 65342-1392?

The NDC code 65342-1392 is assigned by the FDA to the product Tinted Moisturizer Spf-20 Mocha which is product labeled by Gurwitch Products, L.l.c.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 65342-1392-0 40 ml in 1 tube , 65342-1392-1 1 tube in 1 carton / 50 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 Tinted Moisturizer Spf-20 Mocha?

Direction for use : Apply to clean skin with fingertips. Layer for additional coverage.  

Which are Tinted Moisturizer Spf-20 Mocha UNII Codes?

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

Which are Tinted Moisturizer Spf-20 Mocha 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".