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  4. NDC Product Code: 69740-341 Secura Epc Skin Care Starter Kit

NDC 69740-341 Secura Epc Skin Care Starter Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69740-341?
  4. Secura Epc Skin Care Starter Kit 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:
69740-341
Proprietary Name:
Secura Epc Skin Care Starter Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Smith & Nephew Medical Ltd
Labeler Code:
69740
Product Label ID:
645a8c2f-bb27-4dba-8e85-cc1d81b2bb68
Start Marketing Date: [9]
08-01-2003
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 69740-341?

The NDC code 69740-341 is assigned by the FDA to the product Secura Epc Skin Care Starter Kit which is product labeled by Smith & Nephew Medical Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69740-341-00 1 kit in 1 container * 92 g in 1 tube * 118 ml in 1 bottle, spray. 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 Secura Epc Skin Care Starter Kit?

1. Change wet and soiled diapers, garments, and linens promptly. Spray cleanser liberally on affected area. 2. Wipe clean with tissues, and remove soiled underpads and diapers. 3. Immediately dispose of tissues and underpads to control odor. Allow to dry. No rinsing necessary. 4. Apply protective cream liberally as often as necessary with each diaper, garment, or linen change; especially at bedtime or anytime when exposure to soiled diapers, garments, linens, feces or unrine may be prolonged. 5. Check patient often. Repeat steps 1-4 after each exposure to feces and urine. Refer to individual product labeling for detailed instructions. Packaged in the USA with products made in USA and India for:Smith & Nephew Medical Ltd, 101 Hessle Road, Hull HU3 2BN England. www.smith-nephew.com *Trademarks of Smith & Nephew Certain marks reg’d U.S. Pat. and Tm. Off. • apply liberally on affected area, then wipe clean • no rinsing necessary • change wet and soiled diapers, garments, and linens promptly • cleanse the affected area and allow to dry • apply cream liberally as often as necessary with each diaper change; especially at bedtime or anytime when exposure to soiled diapers, garments, linens, feces or urine may be prolonged

Which are Secura Epc Skin Care Starter Kit UNII Codes?

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

Which are Secura Epc Skin Care Starter Kit 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 Secura Epc Skin Care Starter Kit?

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: 1039026 - benzethonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1039026 - benzethonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1045420 - {1 (118 ML) (benzethonium chloride 1.3 MG/ML Medicated Liquid Soap) / 1 (92000 MG) (zinc oxide 306 MG/ML Topical Cream) } Pack
  • RxCUI: 1045420 - benzethonium Cl 0.13 % Medicated Soap (118 ML) / zinc oxide 30.6 % Cream (92 GM) Pack
  • RxCUI: 1045420 - {1 (118 ML benzethonium chloride 0.13 % Medicated Liquid Soap) / 1 (92000 MG zinc oxide 30.6 % Topical Cream) } Pack

* 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".