NDC 78876-712 Wonvia Antibacterial Hand Disinfectant Sanitizer

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:
78876-712
Proprietary Name:
Wonvia Antibacterial Hand Disinfectant Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kaplan Distribution Llc
Labeler Code:
78876
Start Marketing Date: [9]
06-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 78876-712-02

Package Description: 200 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 78876-712?

The NDC code 78876-712 is assigned by the FDA to the product Wonvia Antibacterial Hand Disinfectant Sanitizer which is product labeled by Kaplan Distribution Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78876-712-02 200 ml in 1 bottle, spray . 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 Wonvia Antibacterial Hand Disinfectant Sanitizer?

Use enough amount of product to keep your hands wet. Rub hands together for 30 seconds.Keep away from children, food, and animal feed.Follow the instructions to avoid risks to human and environmental health.

Which are Wonvia Antibacterial Hand Disinfectant Sanitizer UNII Codes?

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

Which are Wonvia Antibacterial Hand Disinfectant Sanitizer 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".