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  4. NDC Product Code: 43116-016 Shierjie 75% Alcohol Pads

NDC 43116-016 Shierjie 75% Alcohol Pads

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43116-016?
  4. Shierjie 75% Alcohol Pads Uses
  5. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
43116-016
Proprietary Name:
Shierjie 75% Alcohol Pads
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:
a6770769-8074-7fcc-e053-2995a90ac0c1
Start Marketing Date: [9]
03-31-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43116-016-01

Package Description: 100 CLOTH in 1 BOX

Product Details

What is NDC 43116-016?

The NDC code 43116-016 is assigned by the FDA to the product Shierjie 75% Alcohol Pads which is product labeled by Shenzhen Shierjie Biological Engineering Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43116-016-01 100 cloth 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 Shierjie 75% Alcohol Pads?

Children under 6 years of age should be supervised when using this product

What is the NDC to RxNorm Crosswalk for Shierjie 75% Alcohol Pads?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".