Home NDC 87725-003 TOTCLEAR NAIL RENEWAL
Product NDC 87725-003
11-digit product format 877250003
Labeler code 87725
Product ID 87725-003_021656fa-185d-47b3-9aaf-5d764e09866c
Type HUMAN OTC DRUG
Nonproprietary name UNDECYLENIC ACID
Dosage form SOLUTION/ DROPS
Route TOPICAL
Labeler GOOD BRIDGE LLC
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-11
Substance UNDECYLENIC ACID
Active strength 300 mg/mL
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 TOTCLEAR NAIL RENEWAL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength UNDECYLENIC ACID 300 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K3D86KJ24N Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2749411 Internal RxNorm 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 40 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87725-003-01 87725000301 20 mL in 1 BOTTLE, WITH APPLICATOR (87725-003-01) 20 ml 2026-08-11 No No Current