FDA.reportPublic FDA data

Terrasil Antifungal Cream Maximum Strength

Manufacturer
Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
Effective date
2025-07-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:35:59

Label at a glance#

ProductTerrasil Antifungal Cream Maximum Strength
Active ingredientCLOTRIMAZOLE
Label structure8 sections

Indications and uses

Cures most fungal skin infections, including ringworm and tinea. For effective relief of itching, scaling, cracking, burning, discoloration, soreness, irritation, discomfort, redness and chafing associated with fungal skin infections.

Dosage and administration

Wash and dry affected skin. Apply a thin layer of cream over the affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. Store at room temperature. May stain fabrics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Clotrimazole 1%

Purpose

OTC - PURPOSE SECTION

Antifungal

Uses

INDICATIONS & USAGE SECTION

Cures most fungal skin infections, including ringworm and tinea. For effective relief of itching, scaling, cracking, burning, discoloration, soreness, irritation, discomfort, redness and chafing associated with fungal skin infections.

Warnings

WARNINGS SECTION

For external use only.

Do not useon 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Wash and dry affected skin. Apply a thin layer of cream over the affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. Store at room temperature. May stain fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

cotton seed oil, distilled water, emulsifying wax, Jojoba seed oil, peppermint oil, shea butter, silver stearate, sorbic acid, tea tree oil, zinc oxide

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24909-20824909-208-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
COTTONSEED OILH3E878020NIACT
PEPPERMINT OILAV092KU4JHIACT
SILVER STEARATE4H6PCL92ZNIACT
TEA TREE OILVIF565UC2GIACT
ZINC OXIDESOI2LOH54ZIACT
JOJOBA OIL724GKU717MIACT
WATER059QF0KO0RIACT
SORBIC ACIDX045WJ989BIACT
SHEA BUTTERK49155WL9YIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CLOTRIMAZOLEG07GZ97H65ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
39b12259-4c11-b66d-e063-6294a90a1e83d0108ec5-8fd9-45d9-8c75-a222ebf82a0e2025-07-11WarningsExact identifier
spl id: 39b12259-4c11-b66d-e063-6294a90a1e83
spl set id: d0108ec5-8fd9-45d9-8c75-a222ebf82a0e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.