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  4. NDC Product Code: 75183-010 Zorari Waterless Disinfection

NDC 75183-010 Zorari Waterless Disinfection

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75183-010?
  4. Zorari Waterless Disinfection 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:
75183-010
Proprietary Name:
Zorari Waterless Disinfection
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zorin Pharmaceutical Technology (hangzhou) Co Ltd.
Labeler Code:
75183
Product Label ID:
321aedfe-04e5-499f-91ca-434d731f24f7
Start Marketing Date: [9]
07-23-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 75183-010?

The NDC code 75183-010 is assigned by the FDA to the product Zorari Waterless Disinfection which is product labeled by Zorin Pharmaceutical Technology (hangzhou) Co Ltd.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 75183-010-01 500 ml in 1 bottle , 75183-010-02 1000 ml in 1 bottle , 75183-010-03 3780 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 Zorari Waterless Disinfection?

Squeeze small amount to your palms and thoroughly spread on both hands. Rub into skin until dry.Other information:Store at 25℃， At low temperature, turbidity and precipitation may occur.

Which are Zorari Waterless Disinfection UNII Codes?

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

Which are Zorari Waterless Disinfection 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".