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  4. NDC Product Code: 75138-130 Aonisen Hand Sanitizer

NDC 75138-130 Aonisen Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75138-130?
  4. Aonisen Hand Sanitizer 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:
75138-130
Proprietary Name:
Aonisen Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Henan Shizheng Pharmaceutical Technology Co., Ltd.
Labeler Code:
75138
Product Label ID:
a2e46b9f-426b-52f1-e053-2995a90aa19c
Start Marketing Date: [9]
02-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 75138-130?

The NDC code 75138-130 is assigned by the FDA to the product Aonisen Hand Sanitizer which is product labeled by Henan Shizheng Pharmaceutical Technology Co., Ltd.. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 75138-130-06 59 ml in 1 bottle, plastic , 75138-130-10 100 ml in 1 bottle, plastic , 75138-130-13 30 ml in 1 bottle, plastic , 75138-130-30 300 ml in 1 bottle, pump , 75138-130-51 500 ml in 1 bottle, pump , 75138-130-52 500 ml in 1 bottle, pump . 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 Aonisen Hand Sanitizer?

Apply enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry.Children under age 6 should be supervised when using this product.

What is the NDC to RxNorm Crosswalk for Aonisen Hand Sanitizer?

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".