Wart Remover Liquid
- Product NDC
- 87298-012
- 11-digit product format
- 872980012
- Labeler code
- 87298
- Product ID
- 87298-012_47783ab1-5e0e-1cc1-e063-6294a90aac33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid
- Dosage form
- LIQUID
- Route
- CUTANEOUS; EXTRACORPOREAL; INTRAEPIDERMAL
- Labeler
- Guangzhou Hechuang Commercial Service Co.,Ltd.
- Application
- M028
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-03
- Substance
- SALICYLIC ACID
- Active strength
- 8 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Wart Remover Liquid
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 8 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ |
| Rxcui | 252577 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87298-012-01 | Wart Remover Liquid | 20 g in 1 BOTTLE, DROPPER | 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 |
|---|
| 87298-012-01 | 87298001201 | 20 g in 1 BOTTLE, DROPPER (87298-012-01) | 20 g | 2026-01-03 | No | No | Current |