NDC 66774-1003 Viroxyn Professional Use

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:
66774-1003
Proprietary Name:
Viroxyn Professional Use
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Quadex Pharmaceuticals Llc
Labeler Code:
66774
Start Marketing Date: [9]
10-22-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 66774-1003-2

Package Description: 2 AMPULE in 1 BLISTER PACK / .6 mL in 1 AMPULE

NDC Code 66774-1003-3

Package Description: 3 AMPULE in 1 BLISTER PACK / .6 mL in 1 AMPULE

NDC Code 66774-1003-4

Package Description: 6 AMPULE in 1 BOX / .6 mL in 1 AMPULE

NDC Code 66774-1003-5

Package Description: 12 AMPULE in 1 BLISTER PACK / .6 mL in 1 AMPULE

Product Details

What is NDC 66774-1003?

The NDC code 66774-1003 is assigned by the FDA to the product Viroxyn Professional Use which is product labeled by Quadex Pharmaceuticals Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 66774-1003-2 2 ampule in 1 blister pack / .6 ml in 1 ampule, 66774-1003-3 3 ampule in 1 blister pack / .6 ml in 1 ampule, 66774-1003-4 6 ampule in 1 box / .6 ml in 1 ampule, 66774-1003-5 12 ampule in 1 blister pack / .6 ml in 1 ampule. 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 Viroxyn Professional Use?

Using only warm water and a washcloth, clean the lip area of any lip preparations, lotions, ointments, residual beverages, or cosmetics, including lipstick.Remove the cardboard cap from the applicator end and place the cardboard cap on to the glass/plastic vial end, opposite the brush end of the product.Squeeze the cardboard cap to break open the inner glass vial.Saturate the applicator end with solution by holding the brush end down and squeezing the container until you can see liquid on the brush applicator.Touch the cold sore with the wet applicator and allow the numbing agent a few moments to numb your lip. Then begin actual treatment.For best results, message the solution into the cold sore by rubbing. Rub firmly, but take care not to damage the tissue. The purpose of the rubbing is to deliver the drug to the infection site. Hold the vial so the solution flows to the sore.To treat most cold sores, usually one treatment is enough. If you symptoms go away and then return later, apply another dose for the second cold sore.Do not use more than 3 times a day.Children under 2 years of age – ask a doctor or dentist.Discard after use.

Which are Viroxyn Professional Use UNII Codes?

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

Which are Viroxyn Professional Use 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 Viroxyn Professional Use?

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: 1545787 - benzalkonium chloride 0.13 % / benzocaine 7.5 % Topical Solution
  • RxCUI: 1545787 - benzalkonium chloride 1.3 MG/ML / benzocaine 75 MG/ML Topical Solution
  • RxCUI: 1545789 - benzalkonium chloride 1.3 MG/ML / benzocaine 75 MG/ML Topical Solution [Viroxyn]
  • RxCUI: 1545789 - Viroxyn (benzalkonium chloride 0.13 % / benzocaine 7.5 % ) Topical Solution

* 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".