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  4. NDC Product Code: 69740-343 Secura Personal Skin Care Kit

NDC 69740-343 Secura Personal Skin Care Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69740-343?
  4. Secura Personal Skin Care 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:
69740-343
Proprietary Name:
Secura Personal Skin Care 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:
eba485f5-b9b0-4580-987d-42354df4810c
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 69740-343?

The NDC code 69740-343 is assigned by the FDA to the product Secura Personal Skin Care 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 69740-343-00 1 kit in 1 carton * 236 ml in 1 bottle, spray * 70 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 Personal Skin Care Kit?

Change wet and soiled diapers, garments, and linens promptly. Spray cleanser liberally on affected area.Wipe clean with tissues, and remove soiled underpads and diapers.Immediately dispose of tissues and underpads to control odor. Allow to dry. No rinsing necessary.Apply protective ointment 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.Check patient often. Repeat steps 1-4 after each exposure to feces and urine. spray cleanser liberally on affected area, then wipe cleanno rinsing necessary change wet and soiled diapers, garments and linens promptlycleanse the affected area and allow to dryapply ointment 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 Personal Skin Care Kit UNII Codes?

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

Which are Secura Personal Skin Care 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 Personal Skin Care 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: 1045424 - {1 (236 ML) (benzethonium chloride 1.3 MG/ML Medicated Liquid Soap) / 1 (72000 MG) (petrolatum 0.988 MG/MG Topical Ointment) } Pack
  • RxCUI: 1045424 - benzethonium Cl 0.13 % Medicated Liquid Soap (236 ML) / petrolatum 98.8 % Topical Ointment (72 GM) Pack
  • RxCUI: 1045424 - {1 (236 ML benzethonium chloride 0.13 % Medicated Liquid Soap) / 1 (72000 MG petrolatum 98.78 % Topical Ointment) } 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".