Home NDC 83818-012 SupreH Bee Venom Skin Tag Treatment Liquid
Product NDC 83818-012
11-digit product format 838180012
Labeler code 83818
Product ID 83818-012_35ca9836-917b-b0ac-e063-6294a90a28a2
Type HUMAN OTC DRUG
Nonproprietary name SupreH Bee Venom Skin Tag Remover Liquid
Dosage form LIQUID
Route TOPICAL
Labeler Shenzhen Xinxin Yunhai Technology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-23
Substance THUJA OCCIDENTALIS WHOLE; APIS MELLIFERA VENOM; CALENDULA OFFICINALIS FLOWER
Active strength 2; 2; 2 g/100mL; g/100mL; 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 SupreH Bee Venom Skin Tag Treatment Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength THUJA OCCIDENTALIS WHOLE 2 g/100mL APIS MELLIFERA VENOM 2 g/100mL CALENDULA OFFICINALIS FLOWER 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5HBV6WCE3N Internal UNII lookup 76013O881M Internal UNII lookup P0M7O4Y7YD 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 83818-012-01 SupreH Bee Venom Skin Tag Treatment Liquid 30 mL in 1 BOTTLE LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83818-012 SUPREH BEE VENOM SKIN TAG TREATMENT LIQUID (SUPREH BEE VENOM SKIN TAG REMOVER LIQUID) LIQUID [SHENZHEN XINXIN YUNHAI TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250527_35ca9836-917a-b0ac-e063-6294a90a28a2.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 38 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 83818-012-01 83818001201 30 mL in 1 BOTTLE (83818-012-01) 30 ml 2025-05-23 No No Current