SottSunFeli Wart Remover
- Product NDC
- 85136-010
- 11-digit product format
- 851360010
- Labeler code
- 85136
- Product ID
- 85136-010_438bde30-3e25-9157-e063-6294a90a1423
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SALICYLIC ACID
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Henan Toudaorong Biotechnology Co., Ltd.
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-14
- Substance
- SALICYLIC ACID
- Active strength
- 15 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
- SottSunFeli Wart Remover
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 15 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 238466 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85136-010-01 | SottSunFeli Wart Remover | 20 mL in 1 BOTTLE | LIQUID | 20 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85136-010-01 | 85136001001 | 20 mL in 1 BOTTLE (85136-010-01) | 20 ml | 2025-11-14 | No | No | Current |