NDC 79518-088 Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant

Benzalkonium Chloride

NDC Product Code 79518-088

NDC CODE: 79518-088

Proprietary Name: Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Benzalkonium Chloride What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 79518 - Core Pacific, Inc.

NDC 79518-088-01

Package Description: 59.14 mL in 1 BOTTLE, SPRAY

NDC 79518-088-02

Package Description: 237 mL in 1 BOTTLE, SPRAY

NDC Product Information

Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant with NDC 79518-088 is a a human over the counter drug product labeled by Core Pacific, Inc.. The generic name of Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant is benzalkonium chloride. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Core Pacific, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BENZALKONIUM CHLORIDE .13 g/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • SILVER (UNII: 3M4G523W1G)
  • SODIUM SESQUICARBONATE (UNII: Y1X815621J)
  • MAGNESIUM (UNII: I38ZP9992A)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Core Pacific, Inc.
Labeler Code: 79518
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 11-01-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant Product Label Images

Dr. Du-mores Viral Defense Nano Silver Skin Disinfectant And Protectant Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses:

Sanitizes and protects skin and surfaces to help reduce viruses and bacteria that cause disease.

Warnings:

For external use only.Do not use in eyes. If contact occurs, flush thoroughly with water.Stop use and ask a doctor: If irritation or redness develops, or if condition persist for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children: If swallowed, get medical help or contact a Poison Control Center.

Directions:

On dry skin, apply enough product to thoroughly cover the areas to be protected and allow to dry. If abrasively washed reapply as needed.

Other Ingredients:

Structured water, nano colloidal silver, sodium sesquicarbonate, magnesium.

* Please review the disclaimer below.