Wart Remover
NDC 88064-123, Wart Remover, liquid, from Shenzhen Baifanghui Technology Co., Ltd.
- Product NDC
- 88064-123
- Status
- Listed
- Labeler
- Shenzhen Baifanghui Technology Co., Ltd
- Dosage form
- LIQUID
- Route
- CUTANEOUS
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/88064-123 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SALICYLIC ACID.4 g/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 88064-123-01 | 88064012301 | 5 BAG in 1 BOX (88064-123-01) / 1 LIQUID in 1 BAG |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 88064-123 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/88064-123 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 88064-123. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.