NDC 75687-112 Viro Fense

Benzalkonium Chloride

NDC Product Code 75687-112

NDC 75687-112-16

Package Description: 473 mL in 1 BOTTLE

NDC 75687-112-28

Package Description: 3785 mL in 1 BOTTLE

NDC 75687-112-40

Package Description: 18927 mL in 1 PAIL

NDC Product Information

Viro Fense with NDC 75687-112 is a a human over the counter drug product labeled by Geopak Solutions, Llc. The generic name of Viro Fense is benzalkonium chloride. The product's dosage form is spray and is administered via topical form.

Labeler Name: Geopak Solutions, Llc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Viro Fense 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.


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)

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: Geopak Solutions, Llc
Labeler Code: 75687
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: 05-01-2020 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.

Viro Fense Product Label Images

Viro Fense 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:

Alkyl Dimethyl Benzyl Ammonium Chloride C12-C18..........................0.25%




Hands sanitizer to help decrease bacteria on the skin and disinfectant spray for cleaning. Recommended for repeated use.


FOR EXTERNAL USE ONLY. DO NOT ingest this product.When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Do not inhale or ingest.STOP use and ask a doctor if irritation or redness develops.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. If swallowed get medical attention right away.


Apply directly to hands and briskly rub all areas especially between the fingers and finger nail area. The active ingredients of this product will help prevent bacterial and viral growth after it dries.

Inactive Ingredient:



Kills 99.99% of GermsREADY TO USEWaterless Hand SanitizerMADE IN USA•Disinfectant• Antimicrobial• Kills bacteria, viruses, fungi, yeast & protozoa• Continued protection after driedGeoPak solutions203 Echelon Road Greenville, SC 29605VirofenseTM is Distributed by:Geoponics3415 Radio Road Unit 105 Naples FL, 34104877 667-6330

* Please review the disclaimer below.