Home NDC 73302-201 Mederma Advanced Scar
Product NDC 73302-201
11-digit product format 733020201
Labeler code 73302
Product ID 73302-201_5916ff73-1d7c-416d-97ad-11038b1b5d2c
Type HUMAN OTC DRUG
Nonproprietary name Allantoin
Dosage form GEL
Route TOPICAL
Labeler PMI Branded Pharmaceuticals, Inc.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-11-01
Marketing end 2027-08-01
Substance ALLANTOIN
Active strength 5 mg/g
NDC exclude flag No
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 Mederma Advanced Scar Active Ingredients# Ingredient, Strength table Ingredient Strength ALLANTOIN 5 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1442087 Internal RxNorm lookup 1442092 Internal RxNorm 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 73302-201-20 Mederma Advanced Scar 1 in 1 BOX GEL 1 5 73302-201-20 Mederma Advanced Scar 20 g in 1 TUBE GEL 20 5 73302-201-50 Mederma Advanced Scar 50 g in 1 TUBE GEL 50 5 73302-201-50 Mederma Advanced Scar 1 in 1 BOX GEL 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73302-201 MEDERMA ADVANCED SCAR (ALLANTOIN) GEL [HRA PHARMA AMERICA, INC.] 5 Current NDC, Legacy NDC, 4 package rows 20250129_25bc1eae-3502-4c63-bd8a-43be2dfb0d6d.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 52 of 68 · 1,357 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 73302-201-20 73302020120 1 TUBE in 1 BOX (73302-201-20) / 20 g in 1 TUBE 1 tube 2013-11-01 2026-11-01 No No Current 73302-201-50 73302020150 1 TUBE in 1 BOX (73302-201-50) / 50 g in 1 TUBE 1 tube 2013-11-01 2027-08-01 No No Current