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NDC 74651-0003 Cona

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74651-0003?
  4. Cona 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:
74651-0003
Proprietary Name:
Cona
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dongbo Bio Co.,ltd
Labeler Code:
74651
Product Label ID:
a408f78a-1d8b-37d0-e053-2995a90a992c
Start Marketing Date: [9]
04-04-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74651-0003?

The NDC code 74651-0003 is assigned by the FDA to the product Cona which is product labeled by Dongbo Bio Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 74651-0003-1 500 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 Cona?

Spray on any area, items, and applications: kitchen, bathroom, living room, bedroom, fitness center, hospital, sanatorium, other medical facilities, restaurants, stores, shoe rack, fabrics, shoes, bags, toys, pet products, stale tobacco smell, moldy smell, sick house syndromeSpray from the point as high as possible to maximize the time of staying in the airPomist care about environmental destruction and do not use any toxic chemicals or unknown substances in its products and manufacturing processesPomist’s patented technology eliminates odor and viruses by neutralizing cation of odor and viruses with its high potency anion and far-infrared release

Which are Cona UNII Codes?

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

Which are Cona 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".