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  4. NDC Product Code: 76245-102 Sk1n Natural Sunscreen Spf 40

NDC 76245-102 Sk1n Natural Sunscreen Spf 40

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76245-102?
  4. Active Ingredients UNII Codes
  5. 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:
76245-102
Proprietary Name:
Sk1n Natural Sunscreen Spf 40
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
True Nature Group, Inc.
Labeler Code:
76245
Product Label ID:
9491e9fa-508b-487c-a325-c50a5a151d6d
Start Marketing Date: [9]
01-01-1996
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 76245-102?

The NDC code 76245-102 is assigned by the FDA to the product Sk1n Natural Sunscreen Spf 40 which is product labeled by True Nature Group, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76245-102-01 142 g 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.

Which are Sk1n Natural Sunscreen Spf 40 UNII Codes?

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

Which are Sk1n Natural Sunscreen Spf 40 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".