NDC 75428-602 Yorun Germicidal Disposable Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75428-602
Proprietary Name:
Yorun Germicidal Disposable Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shandong Baihe Sanitary Products Co., Ltd.
Labeler Code:
75428
Start Marketing Date: [9]
10-24-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75428-602-01

Package Description: 16 DRUM in 1 CARTON / 160 CLOTH in 1 DRUM

Product Details

What is NDC 75428-602?

The NDC code 75428-602 is assigned by the FDA to the product Yorun Germicidal Disposable Wipes which is product labeled by Shandong Baihe Sanitary Products Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75428-602-01 16 drum in 1 carton / 160 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 Yorun Germicidal Disposable Wipes?

Open the cap. Pull out wipe and close the cap. Unfold and wipe hands, fingers and wrists thoroughly and allow to dry. For dirty hands, use first wipe to clean hands then discard wipe; sanitize with second wipe. Discard after single use. Make sure to close the cap firmly after use to retain moisture.

Which are Yorun Germicidal Disposable Wipes UNII Codes?

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

Which are Yorun Germicidal Disposable 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".