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  4. NDC Product Code: 74621-027 Cleace Disinfectant

NDC 74621-027 Cleace Disinfectant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74621-027?
  4. Cleace Disinfectant 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:
74621-027
Proprietary Name:
Cleace Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aogrand International Trade Corporation
Labeler Code:
74621
Product Label ID:
3f3efc84-84bd-42c1-8a1f-b318227b577c
Start Marketing Date: [9]
05-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74621-027?

The NDC code 74621-027 is assigned by the FDA to the product Cleace Disinfectant which is product labeled by Aogrand International Trade Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74621-027-01 100 ml in 1 bottle, plastic , 74621-027-02 500 ml in 1 bottle, plastic . 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 Cleace Disinfectant?

■ clean affected area.■ apply small amount of this product on the area 1 to 3 times daily.■ may be covered with a sterile bandage.■ if bandaged, let dry first.Other information■ Store at room temperature and avoid direct sunlight.■ will produce serious gastric disturbances if taken internally.■ For surface contact that may cause discoloration, test first in areas that are not obvious.

Which are Cleace Disinfectant UNII Codes?

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

Which are Cleace Disinfectant 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".