NDC 78876-710 Wonvia Antibacterial Hand Disinfectant Gel

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:
78876-710
Proprietary Name:
Wonvia Antibacterial Hand Disinfectant Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
78876
Start Marketing Date: [9]
06-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Characteristics

Code Structure Chart

Product Details

What is NDC 78876-710?

The NDC code 78876-710 is assigned by the FDA to the product Wonvia Antibacterial Hand Disinfectant Gel which is product labeled by Kaplan Distribution Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 78876-710-10 1 l in 1 bottle, pump , 78876-710-50 5 l in 1 bottle, pump . 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 Gel?

Use enough amount of solution 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 Gel UNII Codes?

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

Which are Wonvia Antibacterial Hand Disinfectant Gel 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:

What is the NDC to RxNorm Crosswalk for Wonvia Antibacterial Hand Disinfectant Gel?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2381834 - benzalkonium chloride 0.2 % / ethanol 58 % / isopropyl alcohol 12 % Topical Gel
  • RxCUI: 2381834 - benzalkonium chloride 0.002 MG/MG / ethanol 0.58 ML/ML / isopropyl alcohol 0.12 ML/ML Topical Gel

* Please review the disclaimer below.

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".