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  4. NDC Product Code: 75822-027 Amoray

NDC 75822-027 Amoray

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75822-027?
  4. Amoray 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:
75822-027
Proprietary Name:
Amoray
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kozmo Kimya Sanayi Ve Dis Ticaret Limited Sirketi
Labeler Code:
75822
Product Label ID:
a41ebec3-85a4-4fb0-e053-2a95a90a1c4c
Start Marketing Date: [9]
04-26-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 75822-027?

The NDC code 75822-027 is assigned by the FDA to the product Amoray which is product labeled by Kozmo Kimya Sanayi Ve Dis Ticaret Limited Sirketi. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75822-027-03 75 ml in 1 can . 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 Amoray?

This product is used as Cleanse your hands without the use of water and soap. No-rinse alcohol-based.Quickly reduces the number of germs and bacteria after application. Thanks to its special formulation it helps moisturize your skin without irritation.

What is the NDC to RxNorm Crosswalk for Amoray?

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".