NDC 10096-0221 Advance Techniques Keep Clear 2-in-1 Anti-dandruff

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:
10096-0221
Proprietary Name:
Advance Techniques Keep Clear 2-in-1 Anti-dandruff
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avon Products, Inc.
Labeler Code:
10096
Start Marketing Date: [9]
06-14-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10096-0221-1

Package Description: 350 mL in 1 BOTTLE

NDC Code 10096-0221-2

Package Description: 750 mL in 1 BOTTLE

Product Details

What is NDC 10096-0221?

The NDC code 10096-0221 is assigned by the FDA to the product Advance Techniques Keep Clear 2-in-1 Anti-dandruff which is product labeled by Avon Products, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10096-0221-1 350 ml in 1 bottle , 10096-0221-2 750 ml in 1 bottle . 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 Advance Techniques Keep Clear 2-in-1 Anti-dandruff?

Usesreduces the symptoms of dandruffcontrols scalp flaking associated with dandruffhelps prevent recurrence of scalp itching and flaking associated with dandruff.

Which are Advance Techniques Keep Clear 2-in-1 Anti-dandruff UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Advance Techniques Keep Clear 2-in-1 Anti-dandruff?

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:

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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".