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  4. NDC Product Code: 68634-053 Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face

NDC 68634-053 Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68634-053?
  4. Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face 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:
68634-053
Proprietary Name:
Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amcol Health & Beauty Solutions, Inc. Dba
Labeler Code:
68634
Product Label ID:
7720b093-3851-4b92-bef6-222c3e052755
Start Marketing Date: [9]
04-01-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 68634-053?

The NDC code 68634-053 is assigned by the FDA to the product Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face which is product labeled by Amcol Health & Beauty Solutions, Inc. Dba. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68634-053-01 1 tube in 1 carton / 90 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 Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face?

Apply liberally 15 minutes before sun exposure reapply:after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

Which are Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face UNII Codes?

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

Which are Skinpharmacy Advanced Sun Therapy Broad Spectrum Spf 50 Face 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".