Home NDC 87096-003 DRMITSUI SILICONE SCAR REMOVER
Product NDC 87096-003
11-digit product format 870960003
Labeler code 87096
Product ID 87096-003_4c2e9bd9-062e-670d-e063-6294a90ae1f4
Type HUMAN OTC DRUG
Nonproprietary name Silicone
Dosage form GEL
Route CUTANEOUS; TRANSDERMAL
Labeler Zhenping Renren Industry Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-26
Substance DIMETHICONE
Active strength 5 g/100g
Pharmacologic classes Skin Barrier Activity [PE]
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 DRMITSUI SILICONE SCAR REMOVER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE 5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 92RU3N3Y1O 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 87096-003-01 DRMITSUI SILICONE SCAR REMOVER 20 g in 1 TUBE GEL 20 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 87096-003-01 87096000301 20 g in 1 TUBE (87096-003-01) 20 g 2026-01-26 No No Current