Home NDC 24909-207 Terrasil Athletes Foot AntiFungal Treatment Max
Product NDC 24909-207
11-digit product format 249090207
Labeler code 24909
Product ID 24909-207_39b12a97-acad-b756-e063-6294a90aea3a
Type HUMAN OTC DRUG
Nonproprietary name Clotrimazole
Dosage form OINTMENT
Route TOPICAL
Labeler Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-05
Substance CLOTRIMAZOLE
Active strength 1 g/100g
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Terrasil Athletes Foot AntiFungal Treatment Max
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CLOTRIMAZOLE 1 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G07GZ97H65 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 418475 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 24909-207-25 Terrasil Athletes Foot AntiFungal Treatment Max 25 g in 1 TUBE OINTMENT 25 6 24909-207-28 Terrasil Athletes Foot AntiFungal Treatment Max 28 g in 1 TUBE OINTMENT 28 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 24909-207 TERRASIL ATHLETES FOOT ANTIFUNGAL TREATMENT MAX (CLOTRIMAZOLE) OINTMENT [AIDANCE SCIENTIFIC, INC., DBA AIDANCE SKINCARE & TOPICAL SOLUTIONS] 5 Current NDC, Legacy NDC, 2 package rows 20241123_fce478a0-05f5-4606-82ce-c8dd095df211.zip
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 40 of 49 · 973 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 24909-207-25 24909020725 25 g in 1 TUBE (24909-207-25) 25 g 2022-01-05 0000-00-00 No No Current 24909-207-28 24909020728 28 g in 1 TUBE (24909-207-28) 28 g 2024-11-20 No No Current