Home NDC 10738-064 TriDerma Foot Defense
Product NDC 10738-064
11-digit product format 107380064
Labeler code 10738
Product ID 10738-064_49784015-9dd8-090d-e063-6294a90a88e4
Type HUMAN OTC DRUG
Nonproprietary name TriDerma Foot Defense Cream
Dosage form CREAM
Route TOPICAL
Labeler Genuine Virgin Aloe Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-31
Substance ALLANTOIN
Active strength 15 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base TriDerma Foot Defense
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN 15 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 344S277G0Z Internal UNII 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 10738-064-40 TriDerma Foot Defense 1 in 1 CARTON CREAM 1 1 10738-064-45 TriDerma Foot Defense 119 g in 1 TUBE CREAM 119 1
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 10738-064-40 10738006440 1 TUBE in 1 CARTON (10738-064-40) / 119 g in 1 TUBE (10738-064-45) 1 tube 2025-05-31 No No Current 10738-064-45 10738006445 119 g in 1 TUBE 119 g Historical