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  4. NDC Product Code: 63287-425 Fast Results Genital Herpes Treatment

NDC 63287-425 Fast Results Genital Herpes Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63287-425?
  4. Fast Results Genital Herpes Treatment Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63287-425
Proprietary Name:
Fast Results Genital Herpes Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Merix Pharmaceutical Corp.
Labeler Code:
63287
Product Label ID:
5b2beccd-e83e-405a-95c7-ee4d86963655
Start Marketing Date: [9]
06-01-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63287-425-25

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 25 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 63287-425?

The NDC code 63287-425 is assigned by the FDA to the product Fast Results Genital Herpes Treatment which is product labeled by Merix Pharmaceutical Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63287-425-25 1 bottle, spray in 1 box / 25 ml in 1 bottle, spray. 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 Fast Results Genital Herpes Treatment?

Adults or adolescents 12 or older apply to clean dry area free of soap or cleanser residue.

Which are Fast Results Genital Herpes Treatment UNII Codes?

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

Which are Fast Results Genital Herpes Treatment 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 Fast Results Genital Herpes Treatment?

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: 1294436 - benzalkonium Cl 0.13 % / allantoin 0.5 % Topical Spray
  • RxCUI: 1294436 - allantoin 5 MG/ML / benzalkonium chloride 1.3 MG/ML Topical Spray
  • RxCUI: 1294436 - allantoin 0.5 % / benzalkonium Cl 0.13 % Topical Spray

* 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".