FDA.reportPublic FDA data

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
APIS MELLIFERA VENOM; CALENDULA OFFICINALIS FLOWER; THUJA OCCIDENTALIS WHOLE
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

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
IngredientStrength
APIS MELLIFERA VENOM2 g/100mL
CALENDULA OFFICINALIS FLOWER2 g/100mL
THUJA OCCIDENTALIS WHOLE2 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii76013O881M, P0M7O4Y7YD, 5HBV6WCE3N

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83818-012-01SupreH Bee Venom Skin Tag Treatment Liquid30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83818-012SUPREH BEE VENOM SKIN TAG TREATMENT LIQUID (SUPREH BEE VENOM SKIN TAG REMOVER LIQUID) LIQUID [SHENZHEN XINXIN YUNHAI TECHNOLOGY CO., LTD.]1Current NDC, 1 package rows20250527_35ca9836-917a-b0ac-e063-6294a90a28a2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83818-012-018381800120130 mL in 1 BOTTLE (83818-012-01) 30 ml2025-05-23NoNoCurrent