NDC 10157-9012 Blistex Ivarest Medicated Poison Ivy Cleansing Foam

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10157-9012
Proprietary Name:
Blistex Ivarest Medicated Poison Ivy Cleansing Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Blistex Inc
Labeler Code:
10157
Start Marketing Date: [9]
10-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10157-9012-2

Package Description: 177 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 10157-9012?

The NDC code 10157-9012 is assigned by the FDA to the product Blistex Ivarest Medicated Poison Ivy Cleansing Foam 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 10157-9012-2 177 ml in 1 bottle, pump . 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 Ivarest Medicated Poison Ivy Cleansing Foam?

Adults and children 2 years of age and older: apply to affected area, gently rubbing to remove urushiol (toxic plant oil). Rinse under running water.apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: Ask a doctor

Which are Blistex Ivarest Medicated Poison Ivy Cleansing Foam UNII Codes?

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

Which are Blistex Ivarest Medicated Poison Ivy Cleansing Foam 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:

What is the NDC to RxNorm Crosswalk for Blistex Ivarest Medicated Poison Ivy Cleansing Foam?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1482626 - menthol 1 % Medicated Liquid Soap
  • RxCUI: 1482626 - menthol 10 MG/ML Medicated Liquid Soap
  • RxCUI: 1482631 - IVAREST Medicated Poison Ivy Cleansing Foam 1 % Medicated Liquid Soap
  • RxCUI: 1482631 - menthol 10 MG/ML Medicated Liquid Soap [Ivarest Medicated Poison Ivy Cleansing Foam]
  • RxCUI: 1482631 - Ivarest Medicated Poison Ivy Cleansing Foam 1 % Medicated Liquid Soap

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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".