NDC 77878-007 Wipe Out Antibacterial Wipes Lemon Scent

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:
77878-007
Proprietary Name:
Wipe Out Antibacterial Wipes Lemon Scent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tzumi Innovations Llc
Labeler Code:
77878
Start Marketing Date: [9]
06-25-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77878-007-01

Package Description: 20 SOLUTION in 1 BAG

NDC Code 77878-007-02

Package Description: 80 SOLUTION in 1 CANISTER

Product Details

What is NDC 77878-007?

The NDC code 77878-007 is assigned by the FDA to the product Wipe Out Antibacterial Wipes Lemon Scent which is product labeled by Tzumi Innovations Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 77878-007-01 20 solution in 1 bag , 77878-007-02 80 solution in 1 canister . 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 Wipe Out Antibacterial Wipes Lemon Scent?

Wet hands thoroughly with product and allow to dry without wipingFor children under 6, use only under adult supervisionNot recommended for infants

Which are Wipe Out Antibacterial Wipes Lemon Scent UNII Codes?

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

Which are Wipe Out Antibacterial Wipes Lemon Scent 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".