Home NDC 83818-003 Ulensy Corn Callus and Wart Remover
Product NDC 83818-003
11-digit product format 838180003
Labeler code 83818
Product ID 83818-003_0f3353ef-e106-7bd4-e063-6394a90a2562
Type HUMAN OTC DRUG
Nonproprietary name Corn Callus and Wart Remover
Dosage form LIQUID
Route TOPICAL
Labeler Shenzhen Xinxin Yunhai Technology Co., Ltd.
Application M028
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-01-17
Substance SALICYLIC ACID
Active strength 5 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Ulensy Corn Callus and Wart Remover
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198845 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83818-003-01 Ulensy Corn Callus and Wart Remover 20 mL in 1 BOTTLE LIQUID 20 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83818-003 ULENSY CORN CALLUS AND WART REMOVER (CORN CALLUS AND WART REMOVER) LIQUID [SHENZHEN XINXIN YUNHAI TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20240119_0f3353ef-e105-7bd4-e063-6394a90a2562.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 16 of 16 · 305 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83818-003-01 83818000301 20 mL in 1 BOTTLE (83818-003-01) 20 ml 2024-01-17 No No Current