NDC 78122-030 Anti-bacterial Multi-purpose Cleaning 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:
78122-030
Proprietary Name:
Anti-bacterial Multi-purpose Cleaning Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wenzhou Guanshang Paper Co., Ltd
Labeler Code:
78122
Start Marketing Date: [9]
07-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 78122-030-30

Package Description: 30 CLOTH in 1 PACKAGE

Product Details

What is NDC 78122-030?

The NDC code 78122-030 is assigned by the FDA to the product Anti-bacterial Multi-purpose Cleaning Wipes which is product labeled by Wenzhou Guanshang Paper Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78122-030-30 30 cloth in 1 package . 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 Anti-bacterial Multi-purpose Cleaning Wipes?

For use by adults and children 2 years and older. Children under 2 years: consult a doctor before use.

Which are Anti-bacterial Multi-purpose Cleaning Wipes UNII Codes?

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

Which are Anti-bacterial Multi-purpose Cleaning 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:

* Please review the disclaimer below.

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".