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  4. NDC Product Code: 74247-0014 Hanna Disinfectantspray

NDC 74247-0014 Hanna Disinfectantspray

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74247-0014?
  4. Hanna Disinfectantspray Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
74247-0014
Proprietary Name:
Hanna Disinfectantspray
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rainbow Co Ltd
Labeler Code:
74247
Product Label ID:
a7ee6281-8fda-7a28-e053-2995a90a05fd
Start Marketing Date: [9]
06-13-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74247-0014?

The NDC code 74247-0014 is assigned by the FDA to the product Hanna Disinfectantspray which is product labeled by Rainbow Co Ltd. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 74247-0014-1 55 ml in 1 bottle , 74247-0014-2 300 ml in 1 bottle , 74247-0014-3 500 ml in 1 bottle , 74247-0014-4 2000 ml in 1 bottle , 74247-0014-5 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 Hanna Disinfectantspray?

Apply an appropriate amount on your hands and rub well to dry.

Which are Hanna Disinfectantspray UNII Codes?

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

Which are Hanna Disinfectantspray 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:

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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".