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  4. NDC Product Code: 42509-007 Travelshield Sanitizing Wipe

NDC 42509-007 Travelshield Sanitizing Wipe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42509-007?
  4. Travelshield Sanitizing Wipe Uses
  5. 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:
42509-007
Proprietary Name:
Travelshield Sanitizing Wipe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wessco International
Labeler Code:
42509
Product Label ID:
a68e5e5d-0e91-ef8f-e053-2a95a90a97f7
Start Marketing Date: [9]
05-26-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 42509-007?

The NDC code 42509-007 is assigned by the FDA to the product Travelshield Sanitizing Wipe which is product labeled by Wessco International. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 42509-007-01 1 patch in 1 bag / 3.915 ml in 1 patch, 42509-007-02 100 patch in 1 bag / 3.915 ml in 1 patch. 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 Travelshield Sanitizing Wipe?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

What is the NDC to RxNorm Crosswalk for Travelshield Sanitizing Wipe?

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".