Triseptin
NDC Package 70472-101-04

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Triseptin is Surgical Hand ScrubClean under nails with a nail pick. Marketed by Dfb Technology Ltd, this product is identified by NDC 70472-101 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
70472-101-04
Package Description
118 mL in 1 BOTTLE, PLASTIC
Product Code
70472-101
11-Digit Billing Format
70472010104

Clinical Specifications

Proprietary Name
Triseptin
Dosage Form
-
Usage Information
Surgical Hand ScrubClean under nails with a nail pick. Nails should be maintained with a 1 mm free edge.Wet hands and forearms.Dispense palmful (approx. 7 ml) of TRISEPTIN ® Scrub into the palm of one hand. Twist fingertips of the opposite hand, working TRISEPTIN under the nails.Transfer TRISEPTIN to the opposite hand and repeat with fingertips of the other hand.Rub TRISEPTIN over the hands and up the forearms to just past the elbow, paying particular attention to the nails, cuticles and interdigital spaces for 90 seconds.Rinse and repeat. Rinse completely.Patient Preoperative Skin PreparationApply to cleanse the surgical site and surrounding area 12 hours and 6 hours prior to surgery.Clean the surgical area.Place a palmful (approx. 7 ml) of TRISEPTIN to the surgical site and surrounding area and rub for 90 seconds paying particular attention to the surgical area.Rinse and repeat.Rinse completely.

Regulatory & Marketing

Labeler Name
Dfb Technology Ltd
FDA Application #
part333E
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
09-15-2017
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70472-101-04 identifies a specific commercial package of 118 ml in 1 bottle, plastic of Triseptin, labeled by Dfb Technology Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Dfb Technology Ltd on September 15, 2017. The current certification is valid through December 31, 2021.

How is this Dfb Technology Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70472010104. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
70472-101-04
11-Digit CMS (5-4-2)
70472-0101-04

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.