Auronp Wart Remover

Product NDC
85206-005
11-digit product format
852060005
Labeler code
85206
Product ID
85206-005_3e09a7af-4b29-d456-e063-6294a90ad2f8
Type
HUMAN OTC DRUG
Nonproprietary name
GLYCERIN
Dosage form
LIQUID
Route
TOPICAL
Labeler
TT Beauty Trading Co., Ltd.
Application
M016
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-09-05
Substance
APIS MELLIFERA VENOM; LONICERA JAPONICA FLOWER; SOPHORA FLAVESCENS ROOT
Active strength
.03; .03; .03 mg/30mg; mg/30mg; mg/30mg
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Auronp Wart Remover
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
APIS MELLIFERA VENOM.03 mg/30mg
LONICERA JAPONICA FLOWER.03 mg/30mg
SOPHORA FLAVESCENS ROOT.03 mg/30mg

Harmonized Identifiers#

Field, Values table
FieldValues
Unii76013O881M, 4465L2WS4Y, IYR6K8KQ5K

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85206-005-01Auronp Wart Remover30 mg in 1 BOTTLELIQUID301

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85206-005-018520600050130 mg in 1 BOTTLE (85206-005-01) 30 mg2025-09-05NoNoCurrent