Home NDC 84896-002 liquid Wart Corn Callus Remover
Product NDC 84896-002
11-digit product format 848960002
Labeler code 84896
Product ID 84896-002_46218936-4f98-e02e-e063-6394a90a18fb
Type HUMAN OTC DRUG
Nonproprietary name Angelica DAHURICA ROOT
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Mizi Biotechnology Co., LTD.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-27
Substance ANGELICA DAHURICA ROOT; ASIATIC ACID
Active strength .02; .005 g/mL; g/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base liquid Wart Corn Callus Remover
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANGELICA DAHURICA ROOT .02 g/mL ASIATIC ACID .005 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1V63N2S972 Internal UNII lookup 9PA5A687X5 Internal UNII 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 84896-002-01 liquid Wart Corn Callus Remover 30 mL in 1 BOTTLE LIQUID 30 2
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84896-002-01 84896000201 30 mL in 1 BOTTLE (84896-002-01) 30 ml 2025-11-27 No No Current