NDC Package 70472-101-04 Triseptin

View Billable Units, 11-Digit Format, RxNorm

Package Information

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

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70472-101-04
Package Description:
118 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Triseptin
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.
11-Digit NDC Billing Format:
70472010104
Labeler Name:
Dfb Technology Ltd
Sample Package:
No
FDA Application Number:
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 Date:
12-31-2021
Exclude Flag:
I
Code Structure:

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.

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Frequently Asked Questions

What is NDC 70472-101-04?

The NDC Packaged Code 70472-101-04 is assigned to a package of 118 ml in 1 bottle, plastic of Triseptin, labeled by Dfb Technology Ltd. The product's dosage form is and is administered via form.

Is NDC 70472-101 included in the NDC Directory?

No, Triseptin with product code 70472-101 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Dfb Technology Ltd on September 15, 2017 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70472-101-04?

The 11-digit format is 70472010104. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-270472-101-045-4-270472-0101-04