NDC 10096-0238 Mommy Tillia Antibacterial Hand

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:
10096-0238
Proprietary Name:
Mommy Tillia Antibacterial Hand
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avon Products, Inc.
Labeler Code:
10096
Start Marketing Date: [9]
12-20-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10096-0238-1

Package Description: 237 mL in 1 BOTTLE, DISPENSING

Product Details

What is NDC 10096-0238?

The NDC code 10096-0238 is assigned by the FDA to the product Mommy Tillia Antibacterial Hand which is product labeled by Avon Products, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10096-0238-1 237 ml in 1 bottle, dispensing . 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 Mommy Tillia Antibacterial Hand?

Usesfor handwashing to decrease bacteria on the skin

Which are Mommy Tillia Antibacterial Hand UNII Codes?

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

Which are Mommy Tillia Antibacterial Hand 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 Mommy Tillia Antibacterial Hand?

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".