NDC 61715-072 Antiseptic Skin Cleanser

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:
61715-072
Proprietary Name:
Antiseptic Skin Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kinray Inc.
Labeler Code:
61715
Start Marketing Date: [9]
08-03-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61715-072-08

Package Description: 237 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 61715-072?

The NDC code 61715-072 is assigned by the FDA to the product Antiseptic Skin Cleanser which is product labeled by Kinray Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61715-072-08 237 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 Antiseptic Skin Cleanser?

Use with care in premature infants or infants under 2 months of age. These products may cause irritation or chemical burns. Healthcare personnel handwash:wet hands with waterdispense about 5ml of product into cupped hands and wahs in vigorous manner for about 15 secondsrinse and dry thoroughlyPatient preoperative skin preparation:apply product librally to surgical site and swab for at least 2 minutes and dry with a sterile towelrepeat procedure for an additional 2 minutes and dry with a sterile towelSkin wound and normal skin cleansing:thoroughly rinse the area to be cleaned with waterapply the minimum amount of product necessary to cover the skin or wound area and wash gentlyrinse again thoroughly

Which are Antiseptic Skin Cleanser UNII Codes?

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

Which are Antiseptic Skin Cleanser 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 Antiseptic Skin Cleanser?

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: 211365 - chlorhexidine gluconate 4 % Medicated Liquid Soap
  • RxCUI: 211365 - chlorhexidine gluconate 40 MG/ML Medicated Liquid Soap
  • RxCUI: 211365 - chlorhexidine gluconate 4 % Medicated Surgical Scrub

* 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".