NDC 69792-000 Virx-h

NDC Product Code 69792-000

NDC CODE: 69792-000

Proprietary Name: Virx-h 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.

NDC Code Structure

  • 69792 - Medforce Solutions Inc.

NDC 69792-000-01

Package Description: 15 TABLET in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Virx-h with NDC 69792-000 is a product labeled by Medforce Solutions Inc.. The product's dosage form is and is administered via form.

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.

  • CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • WATER (UNII: 059QF0KO0R)
  • ORANGE OIL (UNII: AKN3KSD11B)
  • SUCROSE (UNII: C151H8M554)
  • THIMEROSAL (UNII: 2225PI3MOV)

Product Labeler Information

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

Labeler Name: Medforce Solutions Inc.
Labeler Code: 69792
Start Marketing Date: 05-13-2015 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Virx-h Product Label Images

Virx-h 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

Otc - Active Ingredient

Active Ingredients                     PurposeNaja naja H 10X                    Immune Modulator

Otc - Purpose

Uses: Temporarily reduces joint inflammation and pain and general associated pain

Otc - Keep Out Of Reach Of Children

-Keep out of the reach of children

Indications & Usage

ViRx-HAnti-ViralBrand of Bioven

Dosage & Administration

Directions for Use:Open foil pouchPlace one (1) tab under the tongue to dissolveAllow the tab to dissolve completely (about 30 seconds).Do not swallow the tabAllow several days for the drug to take effect

Warnings

Warnings: for oral use only-side effects may include headache, nausea, sore throat-if symptoms persist stop using this product and consult a physician

Inactive Ingredient

Inactive Ingredients:carboxymethylcellulose, sodium chloride 0.9%, water, orange oil (for flavoring), sucrose, thymerosol

* Please review the disclaimer below.