FDA.reportPublic FDA data

Bangbrek Bee Venom Wart Corn Callus Remover

Product NDC
85792-001
11-digit product format
857920001
Labeler code
85792
Product ID
85792-001_06a7b157-7cc9-4a5d-821c-c55e908687aa
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic acid 17%
Dosage form
LIQUID
Route
TOPICAL
Labeler
Brilliance Trade LLC
Application
M009
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-06-20
Substance
SALICYLIC ACID
Active strength
17 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
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
Bangbrek Bee Venom Wart Corn Callus Remover
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID17 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
O414PZ4LPZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
377946a0-0e8c-70f4-e063-6294a90a1d85Available on FDA.report

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
85792-001-01Bangbrek Bee Venom Wart Corn Callus Remover30 mL in 1 BOXLIQUID304
85792-001-02Bangbrek Bee Venom Wart Corn Callus Remover20 mL in 1 BOXLIQUID204
85792-001-03Bangbrek Bee Venom Wart Corn Callus Remover15 mL in 1 BOXLIQUID154
85792-001-04Bangbrek Bee Venom Wart Corn Callus Remover10 mL in 1 BOXLIQUID104

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 6 of 6 · 107 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Airmit AceDIMENHYDRINATESato Pharmaceutical Co., Ltd.a98d252d-4cfa-496a-ab2c-627f45f0d7d92023-12-01WarningsExact identifier
application number: M009
Meclizine HClMECLIZINE HYDROCHLORIDEBluePoint Laboratoriesd9cae5a6-8d4b-bdaf-e053-2995a90a7d442023-11-17WarningsExact identifier
application number: M009
ZenTrip Motion SicknessMECLIZINE HYDROCHLORIDESato Pharmaceutical Co., LTDbd86c4c7-b6f0-e3e8-e053-2995a90a44542023-11-03WarningsExact identifier
application number: M009
Travel-EaseMECLIZINE HCLGeri-Care Pharmaceutical Corpe3c64eb9-4972-29d9-e053-2a95a90a2a8a2023-10-25WarningsExact identifier
application number: M009
GravolDIMENHYDRINATEChurch & Dwight Co., Inc.d95240bb-02f2-3226-e053-2995a90afacd2022-03-03WarningsExact identifier
application number: M009
Allergy DyeFreeALLERGY DYEFREEAllegiant Health15736bb8-5a5b-489d-83ad-4cf34ec629562021-04-26WarningsExact identifier
application number: M009
Motion Sickness ReliefDIMENHYDRINATE 50MGAllegiant Health7b0aa993-f08f-4dff-a82d-f35b3ebe3cc12019-12-12WarningsExact identifier
application number: M009

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85792-001-018579200010130 mL in 1 BOX (85792-001-01) 30 ml2025-06-20NoNoCurrent
85792-001-028579200010220 mL in 1 BOX (85792-001-02) 20 ml2025-06-20NoNoCurrent
85792-001-038579200010315 mL in 1 BOX (85792-001-03) 15 ml2025-06-20NoNoCurrent
85792-001-048579200010410 mL in 1 BOX (85792-001-04) 10 ml2025-06-20NoNoCurrent