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  4. NDC Product Code: 71389-001 Chlora-cleanze

NDC 71389-001 Chlora-cleanze

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71389-001?
  4. Chlora-cleanze Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
71389-001
Proprietary Name:
Chlora-cleanze
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biotronix Healthcare Industries, Inc.
Labeler Code:
71389
Product Label ID:
4de58778-9aad-54f0-e054-00144ff8d46c
Start Marketing Date: [9]
04-18-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71389-001-01

Package Description: .67 mL in 1 POUCH

NDC Code 71389-001-02

Package Description: 1.5 mL in 1 POUCH

NDC Code 71389-001-03

Package Description: 1.75 mL in 1 POUCH

NDC Code 71389-001-04

Package Description: 3 mL in 1 POUCH

Product Details

What is NDC 71389-001?

The NDC code 71389-001 is assigned by the FDA to the product Chlora-cleanze which is product labeled by Biotronix Healthcare Industries, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 71389-001-01 .67 ml in 1 pouch , 71389-001-02 1.5 ml in 1 pouch , 71389-001-03 1.75 ml in 1 pouch , 71389-001-04 3 ml in 1 pouch . 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 Chlora-cleanze?

Use prior to surgery to prepare patient’s skin. Helps in the reduction of potentially harmful bacteria which can cause skin infections.

Which are Chlora-cleanze UNII Codes?

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

Which are Chlora-cleanze 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 Chlora-cleanze?

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: 1918214 - chlorhexidine gluconate 2 % / isopropyl alcohol 70 % Medicated Pad
  • RxCUI: 1918214 - chlorhexidine gluconate 20 MG/ML / isopropyl alcohol 0.7 ML/ML Medicated Pad
  • RxCUI: 1918214 - chlorhexidine gluconate 2 % / isopropyl alcohol 70 % Topical Swab

* 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".