NDC product
Aesculus 8X
NDC 53645-1932 · True Botanica, LLC
Key facts
| Product NDC | 53645-1932 |
|---|---|
| Proprietary name | Aesculus 8X |
| Nonproprietary name | AESCULUS HIPPOCASTANUM WHOLE |
| Substances | AESCULUS HIPPOCASTANUM WHOLE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | True Botanica, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Marketing start | Jun 16, 2025 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: