Home NDC 84984-004-01 HOUKEA Wart Corn Care Liquid
Product NDC 84984-004
Requested package NDC 84984-004-01
11-digit product format 849840004
Labeler code 84984
Product ID 84984-004_44900cbc-c889-e5c1-e063-6294a90aa0f5
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Houkea Biotechnology Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-04-12
Substance APIS MELLIFERA VENOM; MENTHA PIPERITA LEAF
Active strength .004; .004 mg/20mg; mg/20mg
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 HOUKEA Wart Corn Care Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength APIS MELLIFERA VENOM .004 mg/20mg MENTHA PIPERITA LEAF .004 mg/20mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 76013O881M Internal UNII lookup A389O33LX6 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 84984-004-01 HOUKEA Wart Corn Care Liquid 20 mg in 1 BOTTLE LIQUID 20 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84984-004 HOUKEA WART CORN CARE LIQUID (GLYCERIN) LIQUID [GUANGZHOU HOUKEA BIOTECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250413_328c06ab-986c-8ed8-e063-6394a90adb8e.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 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 84984-004-01 84984000401 20 mg in 1 BOTTLE (84984-004-01) 20 mg 2025-04-12 No No Current