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  4. NDC Product Code: 78641-112 Global Industrial

NDC 78641-112 Global Industrial

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78641-112?
  4. Global Industrial 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:
78641-112
Proprietary Name:
Global Industrial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Global Equipment Company
Labeler Code:
78641
Product Label ID:
be2307d7-45d5-4daf-e053-2a95a90a0483
Start Marketing Date: [9]
01-23-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 78641-112?

The NDC code 78641-112 is assigned by the FDA to the product Global Industrial which is product labeled by Global Equipment Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78641-112-11 100 not applicable in 1 canister / 100 ml in 1 not applicable. 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 Global Industrial?

Wipe hands thoroughly with product, and discard after a single use.Children under 6 years of age should be supervised when using this product.

What is the NDC to RxNorm Crosswalk for Global Industrial?

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".