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  4. NDC Product Code: 43116-026 Shierjie Disinfecting Soft Wipes Antibacterial

NDC 43116-026 Shierjie Disinfecting Soft Wipes Antibacterial

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43116-026?
  4. Shierjie Disinfecting Soft Wipes Antibacterial 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:
43116-026
Proprietary Name:
Shierjie Disinfecting Soft Wipes Antibacterial
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Shierjie Biological Engineering Co., Ltd
Labeler Code:
43116
Product Label ID:
b6a51492-5f14-513e-e053-2995a90a6631
FDA Application Number: [6]
part333A
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date: [9]
03-31-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 43116-026?

The NDC code 43116-026 is assigned by the FDA to the product Shierjie Disinfecting Soft Wipes Antibacterial which is product labeled by Shenzhen Shierjie Biological Engineering Co., Ltd. The product's dosage form is . The product is distributed in 15 packages with assigned NDC codes 43116-026-01 1 cloth in 1 bag , 43116-026-02 10 cloth in 1 bag , 43116-026-03 40 cloth in 1 bag , 43116-026-04 50 cloth in 1 bag , 43116-026-05 60 cloth in 1 bag , 43116-026-06 80 cloth in 1 bag , 43116-026-07 90 cloth in 1 bag , 43116-026-08 100 cloth in 1 bag , 43116-026-09 120 cloth in 1 bag , 43116-026-10 60 cloth in 1 drum , 43116-026-11 80 cloth in 1 drum , 43116-026-12 100 cloth in 1 drum , 43116-026-13 120 cloth in 1 drum , 43116-026-14 160 cloth in 1 drum , 43116-026-15 1000 cloth in 1 drum . 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 Shierjie Disinfecting Soft Wipes Antibacterial?

Decreases bacteria on skin

Which are Shierjie Disinfecting Soft Wipes Antibacterial UNII Codes?

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

Which are Shierjie Disinfecting Soft Wipes Antibacterial 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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".