NDC 42129-114 Anti-bac Antibacterial Hand Wipes Hawaiian Coconut Scented

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:
42129-114
Proprietary Name:
Anti-bac Antibacterial Hand Wipes Hawaiian Coconut Scented
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fustin(xiamen) Commodity Co., Ltd
Labeler Code:
42129
Start Marketing Date: [9]
10-19-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 42129-114-01

Package Description: 2 POUCH in 1 PACKAGE / 1 CLOTH in 1 POUCH

NDC Code 42129-114-02

Package Description: 20 POUCH in 1 BAG / 1 CLOTH in 1 POUCH

NDC Code 42129-114-03

Package Description: 50 CLOTH in 1 BAG

NDC Code 42129-114-04

Package Description: 75 CLOTH in 1 BAG

Product Details

What is NDC 42129-114?

The NDC code 42129-114 is assigned by the FDA to the product Anti-bac Antibacterial Hand Wipes Hawaiian Coconut Scented which is product labeled by Fustin(xiamen) Commodity Co., Ltd. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 42129-114-01 2 pouch in 1 package / 1 cloth in 1 pouch, 42129-114-02 20 pouch in 1 bag / 1 cloth in 1 pouch, 42129-114-03 50 cloth in 1 bag , 42129-114-04 75 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 Anti-bac Antibacterial Hand Wipes Hawaiian Coconut Scented?

Decrease bacteria on hands

Which are Anti-bac Antibacterial Hand Wipes Hawaiian Coconut Scented UNII Codes?

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

Which are Anti-bac Antibacterial Hand Wipes Hawaiian Coconut Scented 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".