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  4. NDC Product Code: 83186-002 Air Purifying Agent

NDC 83186-002 Air Purifying Agent

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83186-002?
  4. Air Purifying Agent 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:
83186-002
Proprietary Name:
Air Purifying Agent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jiangsu Shenying Information Technology Co. Ltd.
Labeler Code:
83186
Product Label ID:
0dca81e9-3b86-4c48-9011-f35b221416fa
Start Marketing Date: [9]
12-16-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 83186-002-01

Package Description: 220 g in 1 BOX

Product Details

What is NDC 83186-002?

The NDC code 83186-002 is assigned by the FDA to the product Air Purifying Agent which is product labeled by Jiangsu Shenying Information Technology Co. Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83186-002-01 220 g in 1 box . 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 Air Purifying Agent?

Avoid contact with eyes and mouth.Suitabke for use in a closed state.The desirable effect will not be achieved in the strong wind condition.Avoid contact with water and fire sources.It can be sealed and preserved if it is not used for a long time.

Which are Air Purifying Agent UNII Codes?

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

Which are Air Purifying Agent 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".