NDC 50563-371 Livegreen Grapefruit 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:
50563-371
Proprietary Name:
Livegreen Grapefruit Antibacterial Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Enchante Accessories Inc.
Labeler Code:
50563
Start Marketing Date: [9]
10-28-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50563-371-01

Package Description: 30 SOLUTION in 1 PACKET

Product Details

What is NDC 50563-371?

The NDC code 50563-371 is assigned by the FDA to the product Livegreen Grapefruit Antibacterial Hand Wipes which is product labeled by Enchante Accessories Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50563-371-01 30 solution in 1 packet . 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 Livegreen Grapefruit Antibacterial Hand Wipes?

For adults and children two years and overPeel over reusable label and remove a wipe from the packet.Wet hands thoroughly and air dry. Place used wipes in to waste basket.  Do not flush.

Which are Livegreen Grapefruit Antibacterial Hand Wipes UNII Codes?

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

Which are Livegreen Grapefruit 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".