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  4. NDC Product Code: 10157-9825 Blistex Five Star

NDC 10157-9825 Blistex Five Star

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10157-9825?
  4. Blistex Five Star Uses
  5. Active 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:
10157-9825
Proprietary Name:
Blistex Five Star
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blistex Inc
Labeler Code:
10157
Product Label ID:
4ac5fb30-359a-4059-871d-3142860460b6
Start Marketing Date: [9]
05-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 10157-9825?

The NDC code 10157-9825 is assigned by the FDA to the product Blistex Five Star which is product labeled by Blistex Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10157-9825-1 1 stick in 1 box . 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 Blistex Five Star?

This product is used as SKIN PROTECTANT/ SUNSCREEN

Which are Blistex Five Star UNII Codes?

The UNII codes for the active 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".