NDC 24909-148 Terrasil S.o.s. Formula

NDC Product Code 24909-148

NDC CODE: 24909-148

Proprietary Name: Terrasil S.o.s. Formula 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

NDC 24909-148-14

Package Description: 14 g in 1 JAR

NDC 24909-148-44

Package Description: 44 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 S.o.s. Formula with NDC 24909-148 is a product labeled by Aidance Skincare & Topical Solutions, Llc. 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.

  • JOJOBA OIL (UNII: 724GKU717M)
  • JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
  • MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
  • PALMAROSA OIL (UNII: 0J3G3O53ST)
  • SILVER OXIDE (UNII: 897WUN6G6T)
  • WHITE WAX (UNII: 7G1J5DA97F)
  • ZINC OXIDE (UNII: SOI2LOH54Z)

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: 05-13-2014 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 S.o.s. Formula Product Label Images

Terrasil S.o.s. Formula 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 Ingredients

Natrum Muriaticum 6X HPUS, Ranunculus Bulbosus 10X HPUSThe letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States

Purpose

Natrum Muriaticum - Zoster Shingle Symptom ReliefRanunculus Bulbosus - Zoster Shingle Blisters, Stinging Pain

Uses

Symptomatic treatment of shingles

Warnings

For external use only.Virally based infections are contagious. This product will not stop the spread of viral infections.Do not use - in the eyes - over large areas of the body - if you are allergic to any ingredient in this product. Ask a doctor before use if pregnant or nursing.Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.

Keep Out Of Reach Of Children.

If swallowed, call poison control or seek medical help.

Directions

Wash and dry affected skin. Apply a thin layer of Terrasil. Repeat procedure 2-3 times daily until symptoms are relieved. Store at room temperature.

Inactive Ingredients

Cera alba (organic beeswax), juniperus virginiana (cedarwood) oil, magnesium oxide, palmarosa oil, silver oxide, simmondsia chinensis (jojoba) seed oil, zinc oxide

* Please review the disclaimer below.