1. Home
  2. Labeler Index
  3. Blistex Inc.
  4. NDC Product Code: 10157-9831 Blistex Lip Vibrance

NDC 10157-9831 Blistex Lip Vibrance

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10157-9831?
  4. Blistex Lip Vibrance 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:
10157-9831
Proprietary Name:
Blistex Lip Vibrance
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blistex Inc.
Labeler Code:
10157
Product Label ID:
efc150e3-56e9-45bb-9064-951d5f665682
Start Marketing Date: [9]
05-31-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 10157-9831?

The NDC code 10157-9831 is assigned by the FDA to the product Blistex Lip Vibrance 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 10157-9831-1 1 cylinder in 1 blister pack / 3.69 g in 1 cylinder. 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 Lip Vibrance?

Apply liberally 15 minutes before sun exposurereapply at least every 2 hoursuse a water resistant sunscreen if swimming or sweatingchildren under 6 months of age: Ask a doctor

Which are Blistex Lip Vibrance UNII Codes?

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

Which are Blistex Lip Vibrance 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:

* 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".