NDC 24909-108 Terrasil Cold Sore Treatment Max

NDC Product Code 24909-108

NDC CODE: 24909-108

Proprietary Name: Terrasil Cold Sore Treatment Max 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

  • 24909 - Aidance Skincare & Topical Solutions, Llc

NDC 24909-108-14

Package Description: 14 g in 1 JAR

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

NDC Product Information

Terrasil Cold Sore Treatment Max with NDC 24909-108 is a product labeled by Aidance Skincare & Topical Solutions, Llc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1250631.

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.


Product Labeler Information

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

Labeler Name: Aidance Skincare & Topical Solutions, Llc
Labeler Code: 24909
Start Marketing Date: 09-07-2012 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: 12-31-2018 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.

Terrasil Cold Sore Treatment Max Product Label Images

Terrasil Cold Sore Treatment Max 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

Allantoin 1.0%, Benzalkonium Chloride 0.13%


Allantoin - Skin ProtectantBenzalkonium Chloride - Cold sore / fever blister treatment; Topical Antiseptic


  • To treat cold sores /
  • Fever blisters.To help guard against
  • Infection.


For external use only. Do not use in the eyes over large areas of the body if you are allergic to any ingredient in this product longer than one week unless directed by doctor Stop use and ask doctor if condition persists or worsens symptoms persist for more than 7 days. Ask a doctor if used to treat deep or puncture wounds, animal bites or serious burns you are pregnant or nursing. When using this product you may feel a brief stinging sensation when you apply it. The stinging should go away in a short time.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a poison control center right away.


Adults and children 12 years or over: Wash hands before and after applying Terrasil. Apply to affected area on face or lips at the first sign of cold sore/fever blister (tingle). Early treatment ensures the best results. Rub in gently but completely. Do not use more than 3 times a day. Children under 12 years: ask a doctor. Store at room temperature.

Inactive Ingredients

Bentonite, cera alba (organic beeswax), magnesium oxide, palmarosa oil, peppermint oil, silver oxide, simmondsia chinensis (jojoba) seed oil, zinc oxide

* Please review the disclaimer below.