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  4. NDC Product Code: 75328-301 Disinfecting Wipes

NDC 75328-301 Disinfecting Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75328-301?
  4. Disinfecting Wipes 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:
75328-301
Proprietary Name:
Disinfecting Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Crown (yangzhou) Health & Beauty Co., Ltd.
Labeler Code:
75328
Product Label ID:
aae0c17f-985e-a9bc-e053-2995a90a9bb2
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 75328-301?

The NDC code 75328-301 is assigned by the FDA to the product Disinfecting Wipes which is product labeled by Crown (yangzhou) Health & Beauty Co., Ltd.. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 75328-301-01 1 cloth in 1 bag , 75328-301-02 10 cloth in 1 bag , 75328-301-03 20 cloth in 1 bag , 75328-301-04 30 cloth in 1 bag , 75328-301-05 50 cloth in 1 bag , 75328-301-06 75 cloth in 1 bag , 75328-301-07 80 cloth in 1 bag , 75328-301-08 100 cloth in 1 bag , 75328-301-09 120 cloth in 1 bag , 75328-301-10 160 cloth in 1 bag . 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 Disinfecting Wipes?

Wipe the surface of the skin and let it air dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Disinfecting Wipes UNII Codes?

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

Which are Disinfecting Wipes 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".