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  4. NDC Product Code: 69740-344 Secura Two Step Kit

NDC 69740-344 Secura Two Step Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69740-344?
  4. Secura Two Step 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:
69740-344
Proprietary Name:
Secura Two Step 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:
92e2a1b5-a5ca-4224-a5db-539e3c43d241
Start Marketing Date: [9]
08-01-2003
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 69740-344?

The NDC code 69740-344 is assigned by the FDA to the product Secura Two Step 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 69740-344-00 1 kit in 1 carton * 236 ml in 1 bottle, spray * 78 g in 1 tube. 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 Two Step Kit?

Good skin care can help prevent breakdown.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 urine 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 & NephewCertain marks  reg'd U.S. Pat. & Tm. Off. apply cleanser liberally on affected area, then wipe cleanno 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, garment or linen change; especially at bedtime or anytime when exposure to soiled diapers, garments, linens, feces or urine may be prolonged

Which are Secura Two Step Kit UNII Codes?

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

Which are Secura Two Step 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 Two Step 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: 1045430 - {1 (236 ML) (benzethonium chloride 1.3 MG/ML Medicated Liquid Soap) / 1 (78000 MG) (zinc oxide 100 MG/ML Topical Cream) } Pack
  • RxCUI: 1045430 - benzethonium Cl 0.13 % Medicated Liquid Soap (236 ML) / zinc oxide 10 % Topical Cream (78 GM) Pack
  • RxCUI: 1045430 - {1 (236 ML benzethonium chloride 0.13 % Medicated Liquid Soap) / 1 (78000 MG zinc oxide 10 % Topical Cream) } Pack

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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".