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  4. NDC Product Code: 74653-105 Micro Guard 24 Hour Surface And Hand Sanitizer

NDC 74653-105 Micro Guard 24 Hour Surface And Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74653-105?
  4. Micro Guard 24 Hour Surface And Hand Sanitizer 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:
74653-105
Proprietary Name:
Micro Guard 24 Hour Surface And Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Meroven Llc
Labeler Code:
74653
Product Label ID:
0f2dd381-369f-4d61-a547-6e9ea69e072c
Start Marketing Date: [9]
06-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74653-105?

The NDC code 74653-105 is assigned by the FDA to the product Micro Guard 24 Hour Surface And Hand Sanitizer which is product labeled by Meroven Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 74653-105-21 80 ml in 1 bottle , 74653-105-22 500 ml in 1 bottle , 74653-105-23 1000 ml in 1 bottle , 74653-105-24 3000 ml in 1 bottle , 74653-105-25 5000 ml in 1 bottle . 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 Micro Guard 24 Hour Surface And Hand Sanitizer?

Usessurfaces and hand sanitizer to decrease bacteria on the skin and surfacesrecommended for repeated usefor use when soap and water are not available

What is the NDC to RxNorm Crosswalk for Micro Guard 24 Hour Surface And Hand Sanitizer?

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".