SupreH Bee Venom Wart Corn Treatment
- Product NDC
- 83818-005
- 11-digit product format
- 838180005
- Labeler code
- 83818
- Product ID
- 83818-005_254581ab-45b6-21fe-e063-6394a90a42c7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Bee Venom Wart Corn Treatment
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Shenzhen Xinxin Yunhai Technology Co., Ltd.
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-10-25
- Substance
- APIS MELLIFERA VENOM; SALICYLIC ACID
- Active strength
- .5; 1.5 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 Wart Corn Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| APIS MELLIFERA VENOM | .5 g/100mL |
| SALICYLIC ACID | 1.5 g/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 76013O881M | Internal UNII lookup |
| O414PZ4LPZ | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 254581ab-45b5-21fe-e063-6394a90a42c7 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| dea2eded-d1e7-46bb-9a3d-f8dc20de6277 | Product name | 1 | 20190408 |
| 48747306-602a-42cc-957b-5b0c69158eee | Product name | 1 | 20180604 |
| db5ebcdb-b6ae-21cd-4dc5-76cd84b5578b | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83818-005-01 | SupreH Bee Venom Wart Corn Treatment | 20 mL in 1 BOTTLE | LIQUID | 20 | 1 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ulensy Corn Callus and Wart Remover | CORN CALLUS AND WART REMOVER | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 0f3353ef-e105-7bd4-e063-6394a90a2562 | 2024-01-18 | Warnings | M028 |
| WARTRIN Wart Remover | SALICYLIC ACID | BALBOA COMPANIES LLC | 62c99f48-3dc1-4b41-8bc4-e93e2decadd9 | 2023-11-11 | Warnings | M028 |
| UFORIC Wart Remover | SALICYLIC ACID | UFORIC HEALTH LLC | 0d06cac6-5296-4d8a-b59e-966baac6be5f | 2023-11-06 | Warnings | M028 |
| WARTOVIR Wart Remover | SALICYLIC ACID | BALBOA COMPANIES LLC | 2dbf5b40-d759-4c37-8dfe-3b65a7e6dbb6 | 2023-11-06 | Warnings | M028 |
| VerruStat Wart Remover | SALICYLIC ACID | Clinical Therapeutic Solutions | 16607d6e-6a5f-4b03-b38c-3610aef9b165 | 2023-11-05 | Warnings | M028 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 83818-005-01 | 83818000501 | 20 mL in 1 BOTTLE (83818-005-01) | 20 ml | 2024-10-25 | No | No | Current |