1. Home
  2. Labeler Index
  3. Abaco Partners Llc Dba Surefil
  4. NDC Product Code: 20890-0100 Topcare Antibacterial Berry Blast Foaming Hand

NDC 20890-0100 Topcare Antibacterial Berry Blast Foaming Hand

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 20890-0100?
  5. Topcare Antibacterial Berry Blast Foaming Hand Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
20890-0100
Proprietary Name:
Topcare Antibacterial Berry Blast Foaming Hand
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Abaco Partners Llc Dba Surefil
Labeler Code:
20890
Product Label ID:
044562bc-ff6d-42af-beb1-0b61b0d0ac83
Start Marketing Date: [9]
08-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)

Product Packages

NDC Code 20890-0100-1

Package Description: 221 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 20890-0100?

The NDC code 20890-0100 is assigned by the FDA to the product Topcare Antibacterial Berry Blast Foaming Hand which is product labeled by Abaco Partners Llc Dba Surefil. The product's dosage form is . The product is distributed in a single package with assigned NDC code 20890-0100-1 221 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 Topcare Antibacterial Berry Blast Foaming Hand?

Pump into to dry hands, vigorously work into a lather and rinse thoroughly.

Which are Topcare Antibacterial Berry Blast Foaming Hand UNII Codes?

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

Which are Topcare Antibacterial Berry Blast Foaming 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 Topcare Antibacterial Berry Blast Foaming 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:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap

* 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".