FDA NDC Directory · JSON-LD · Markdown
NDC 87710-002 · HUMAN OTC DRUG · LIQUID
| Labeler / Manufacturer | Guangzhou Huanmei Cosmetics Co., Ltd |
|---|---|
| Marketing category | Unapproved drug (not FDA-reviewed) |
| Dosage form / route | LIQUID · CUTANEOUS |
| Active ingredients | BENZYL ALCOHOL (.9 mg/100mg) |
| Marketing started | 20260820 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).