OTC Medication Information: Terrasil Anti-Fungal Treatment MAX

TERRASIL ANTI-FUNGAL TREATMENT MAX- clotrimazole ointment
Aidance Skincare & Topical Solutions, LLC

Active Ingredient

Clotrimazole 1%

Purpose

Antifungal

Uses

Proven clinically effective in the treatment of athlete’s foot (tinea pedis), jock itch (tinea cruris), ringworm (tinea corporis). For effective relief of itching, irritation, redness, scaling, cracking, burning, soreness, and discomfort which can accompany these conditions.

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 2 weeks, discontinue use and consult a physician. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wash and dry affected skin. Apply a layer of ointment over affected area twice daily or as directed by a doctor. Supervise children in the use of this product.

Inactive Ingredients

beeswax, coconut oil (organic), cottonseed oil, jojoba oil, magnesium oxide, MCT oil, peppermint oil, sage oil, silver stearate, tea tree oil, witch hazel, zinc oxide

Other information

Store at room temperature. May temporarily (washable) discolor skin and fabrics in sunlight.

Product label

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TERRASIL ANTI-FUNGAL TREATMENT MAX
clotrimazole ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:24909-106
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLOTRIMAZOLE (CLOTRIMAZOLE) CLOTRIMAZOLE 1 g in 100 g
Inactive Ingredients
Ingredient Name Strength
YELLOW WAX
COCONUT OIL
COTTONSEED OIL
JOJOBA OIL
MAGNESIUM OXIDE
PALM OIL
PEPPERMINT OIL
SAGE OIL
SILVER STEARATE
TEA TREE OIL
WITCH HAZEL
ZINC OXIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:24909-106-14 14 g in 1 JAR None
2 NDC:24909-106-44 44 g in 1 JAR None
3 NDC:24909-106-15 14 g in 1 TUBE None
4 NDC:24909-106-50 50 g in 1 TUBE None
5 NDC:24909-106-20 200 g in 1 JAR None
6 NDC:24909-106-10 10 g in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M005 09/07/2012
Labeler — Aidance Skincare & Topical Solutions, LLC (018950611)
Establishment
Name Address ID/FEI Operations
Aidance Skincare & Topical Solutions, LLC 018950611 manufacture (24909-106)

Revised: 11/2023 Aidance Skincare & Topical Solutions, LLC

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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