0.9% Benzyl Alcohol Solution (Laboratory Use Only)
NDC 87710-002, 0.9% Benzyl Alcohol Solution (Laboratory Use Only), liquid, from Guangzhou Huanmei Cosmetics Co., Ltd.
- Product NDC
- 87710-002
- Status
- Listed
- Labeler
- Guangzhou Huanmei Cosmetics Co., Ltd
- Dosage form
- LIQUID
- Route
- CUTANEOUS
- Product type
- HUMAN OTC DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/87710-002 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BENZYL ALCOHOL.9 mg/100mg
Pharmacologic classes
Pediculicide [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 87710-002-01 | 87710000201 | 1 BOTTLE in 1 BOX (87710-002-01) / 30 mg in 1 BOTTLE |
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 87710-002 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/87710-002 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 87710-002. 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.