NDC 70472-102 Triseptin Water Aided

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:
70472-102
Proprietary Name:
Triseptin Water Aided
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dfb Technology Ltd
Labeler Code:
70472
Start Marketing Date: [9]
08-25-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF-WHITE)

Product Packages

NDC Code 70472-102-32

Package Description: 946 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 70472-102?

The NDC code 70472-102 is assigned by the FDA to the product Triseptin Water Aided which is product labeled by Dfb Technology Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70472-102-32 946 ml in 1 bottle, plastic . 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 Triseptin Water Aided?

Clean 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 the procedure to just below the elbows.Rinse completely.

Which are Triseptin Water Aided UNII Codes?

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

Which are Triseptin Water Aided 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 Triseptin Water Aided?

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".