Home NDC 10738-920 TriDerma LipSore Relief Cream
Product NDC 10738-920
11-digit product format 107380920
Labeler code 10738
Product ID 10738-920_57a00c43-2fbd-5dd8-e063-6394a90a662f
Type HUMAN OTC DRUG
Nonproprietary name Allantoin Cream
Dosage form CREAM
Route TOPICAL
Labeler Genuine Virgin Aloe Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-20
Substance ALLANTOIN
Active strength 1.5 g/100g
NDC exclude flag No
Listing certified through 2027-12-31
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 TriDerma LipSore Relief Cream
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.
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 10738-920-50 10738092050 1 TUBE in 1 PACKAGE (10738-920-50) / 14 g in 1 TUBE (10738-920-55) 1 tube 2026-07-20 No No Current