Home NDC 84989-006 XIMONTH Bee Venom Repair
Product NDC 84989-006
11-digit product format 849890006
Labeler code 84989
Product ID 84989-006_448b75a9-c28f-bda3-e063-6294a90a3b3b
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form LIQUID
Route TOPICAL
Labeler Shantou Ximonth Biotechnology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-19
Substance APIS MELLIFERA VENOM
Active strength .004 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 XIMONTH Bee Venom Repair
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength APIS MELLIFERA VENOM .004 mg/20mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 76013O881M 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 84989-006-01 XIMONTH Bee Venom Repair 20 mg in 1 BOX LIQUID 20 2
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 30 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84989-006-01 84989000601 20 mg in 1 BOX (84989-006-01) 20 mg 2025-06-19 No No Current