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  4. NDC Product Code: 78785-001 Virus Gone

NDC 78785-001 Virus Gone

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78785-001?
  4. Virus Gone Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
78785-001
Proprietary Name:
Virus Gone
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pure Syncore Llc
Labeler Code:
78785
Product Label ID:
ab24a832-df5c-6ca6-e053-2995a90a8525
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 78785-001?

The NDC code 78785-001 is assigned by the FDA to the product Virus Gone which is product labeled by Pure Syncore Llc. The product's dosage form is . The product is distributed in 10 packages with assigned NDC codes 78785-001-01 500 ml in 1 bottle , 78785-001-02 1000 ml in 1 bottle , 78785-001-03 3785 ml in 1 bottle , 78785-001-04 1000000 ml in 1 tank , 78785-001-05 50 applicator in 1 box / .85 ml in 1 applicator (78785-001-06), 78785-001-07 2000 ml in 1 bottle , 78785-001-08 235 ml in 1 bottle , 78785-001-09 236 ml in 1 bottle , 78785-001-10 354 ml in 1 bottle , 78785-001-11 1892 ml in 1 bottle . 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 Virus Gone?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Virus Gone UNII Codes?

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

Which are Virus Gone 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".