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Terrasil joint pain cream - Medication Information

Product NDC Code 24909-198
Drug Name

Terrasil joint pain cream

Type Brand
Active Ingredients
Menthol, unspecified form 4 g/100g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 1148430
Application Number M017
Labeler Name Aidance Skincare & Topical Solutions, LLC
Packages
Package NDC Code Description
24909-198-01 44 g in 1 jar (24909-198-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Menthol 4%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Adults and children 12 years of age and older. Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age - consult a physician. May stain fabrics.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Chamomile oil, cotton seed oil, emulsifying wax, jojoba oil, magnesium oxide, olive oil, purified water, sage oil, shea butter, silver stearate, sorbic acid (preservative), vitamin B oil, zinc oxide.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Temporarily relieves minor aches and pains of muscles and joints associated with strains.

Purpose

Information about the drug product’s indications for use.
Purpose Topical Analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Terrasil Joint Pain Cream Menthol COTTONSEED OIL JOJOBA OIL CHAMOMILE FLOWER OIL MAGNESIUM OXIDE OLIVE OIL WATER SAGE OIL SHEA BUTTER ZINC OXIDE SORBIC ACID SILVER OXIDE PANTHENOL CETYL STEARATE MENTHOL, UNSPECIFIED FORM MENTHOL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Product label image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
401-432-7750 or www.aidance.com

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed consult a physician.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only. Do not use on wounds or damaged skin and avoid contact with eyes. If contact occurs, rinse thoroughly with water. Keep out of reach of children. If swallowed consult a physician.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API