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Terrasil antifungal cleansing bar - Medication Information

Product NDC Code 24909-037
Drug Name

Terrasil antifungal cleansing bar

Type Brand
Pharm Class Azole Antifungal [EPC],
Azoles [CS]
Active Ingredients
Clotrimazole 1 g/100g
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 251267
Application Number M005
Labeler Name Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Packages
Package NDC Code Description
24909-037-75 75 g in 1 box (24909-037-75)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Purpose Clotrimazole 1% Antifungal

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 Wash affected area daily. For best results use with terrasil Antifungal ointment products.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients beeswax, coconut oil, glycerin, jojoba oil, lauric acid, lavender oil, magnesium oxide, olive oil, pentasodium pentetate, peppermint oil, shea butter (butyrospermum), silver stearate, sodium chloride, sodium citrate, sodium laurate, sodium laureth sulfate, sodium lauryl sulfate, sodium myristate, sodium oleate, sodium olivate, sodium stearate, sorbitol, tea tree oil, tetrasodium etidronate, titanium dioxide, water, 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 For relief of most fungal skin infection symptoms.

Spl product data elements

Usually a list of ingredients in a drug product.
terrasil Antifungal Cleansing Bar CLOTRIMAZOLE YELLOW WAX COCONUT OIL JOJOBA OIL GLYCERIN LAURIC ACID LAVENDER OIL MAGNESIUM OXIDE OLIVE OIL PENTASODIUM PENTETATE PEPPERMINT OIL SHEA BUTTER SODIUM CHLORIDE SODIUM CITRATE SODIUM LAURATE SODIUM LAURETH SULFATE SODIUM LAURYL SULFATE SODIUM MYRISTATE SODIUM OLEATE SODIUM OLIVATE SODIUM STEARATE SORBITOL TEA TREE OIL ETIDRONATE TETRASODIUM TITANIUM DIOXIDE WATER ZINC OXIDE SILVER STEARATE CLOTRIMAZOLE CLOTRIMAZOLE

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

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 children under two years of age unless directed by a physician. Avoid contact with the eyes. If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a physician. Keep out of reach of children . If swallowed, call poison control or seek medical help.

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