Home NDC 10738-026 TriDerma Genuine Aloe Burn
Product NDC 10738-026
11-digit product format 107380026
Labeler code 10738
Product ID 10738-026_49b5961f-d9ba-d80b-e063-6394a90a42fc
Type HUMAN OTC DRUG
Nonproprietary name Aloe Burn Relief
Dosage form CREAM
Route TOPICAL
Labeler Genuine Virgin Aloe Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-01
Substance ALLANTOIN
Active strength 1.5 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base TriDerma Genuine Aloe Burn
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN 1.5 g/100g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10738-026-20 TriDerma Genuine Aloe Burn 1 in 1 PACKAGE CREAM 1 1 10738-026-25 TriDerma Genuine Aloe Burn 56.7 g in 1 TUBE CREAM 56.7 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 10738-026-20 10738002620 1 TUBE in 1 PACKAGE (10738-026-20) / 56.7 g in 1 TUBE (10738-026-25) 1 tube 2026-01-01 No No Current 10738-026-25 10738002625 56.7 g in 1 TUBE 56.7 g Historical