NDC 72363-005 Banda-sil Liquid Gel

Argentum Metallicum

NDC Product Code 72363-005

NDC 72363-005-03

Package Description: 1 BOTTLE, SPRAY in 1 BOX > 28.5 g in 1 BOTTLE, SPRAY

NDC Product Information

Banda-sil Liquid Gel with NDC 72363-005 is a a human over the counter drug product labeled by Ag Essence Inc. The generic name of Banda-sil Liquid Gel is argentum metallicum. The product's dosage form is gel and is administered via topical form.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Banda-sil Liquid Gel 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.

Product Labeler Information

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

Labeler Name: Ag Essence Inc
Labeler Code: 72363
Marketing Category: UNAPPROVED HOMEOPATHIC - 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: 06-25-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 11-30-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N - NO 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".

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Banda-sil Liquid Gel Product Label Images

Banda-sil Liquid Gel 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

Dosage & Administration

Directions For Use:Clear wound area of dirt and debris.Spray the affected area with Banda-Sil Silver Liquid Gel Spray and allow to dry.Cover with a sterile gauze or appropriate secondary dressing and secure in place.Reapply 1-3 times daily or as needed.Between dressing changes maintain a moist wound environment.


Warnings:For External Use Only. Keep out of reach of children.Consult a doctor if condition worsens or does not improve in seven (7) days. Ask a doctor before use if you have deep or puncture wounds, serious bleeding, or servious burns.

Inactive Ingredient

Inactive Ingredients:Complex AG21, Water, Polycationic Polymers, Glycerin, L-Arginine

Indications & Usage

Indications for use:For relief of these symptoms due to minor wounds, burns, scrapes ulcerations,or minor infections, burning, stinging, itching, redness, minor pain, minor inflammation.

Otc - Keep Out Of Reach Of Children

Warnings:For External Use Only. Keep out of reach of children.

Otc - Purpose

Topical Antiseptic

Otc - Active Ingredient

Active IngredientArgentum Metallicum (Metallic Silver 10X 20X 30X HPUS)

* Please review the disclaimer below.