NDC 79178-201 T.m. Green Life Antibacterial Hand 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:
79178-201
Proprietary Name:
T.m. Green Life Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Np Korea
Labeler Code:
79178
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 79178-201-10

Package Description: 10 SWAB in 1 PACKAGE

NDC Code 79178-201-20

Package Description: 20 SWAB in 1 PACKAGE

NDC Code 79178-201-60

Package Description: 60 SWAB in 1 PACKAGE

Product Details

What is NDC 79178-201?

The NDC code 79178-201 is assigned by the FDA to the product T.m. Green Life Antibacterial Hand Wipes which is product labeled by Np Korea. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 79178-201-10 10 swab in 1 package , 79178-201-20 20 swab in 1 package , 79178-201-60 60 swab 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 T.m. Green Life Antibacterial Hand Wipes?

Adults and children 2 years and over; Apply wipe thoroughly to hands. Allow to dry without wiping. Children under 2 years, ask a doctor before use.

Which are T.m. Green Life Antibacterial Hand Wipes UNII Codes?

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

Which are T.m. Green Life Antibacterial Hand 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".