NDC product
Witch Hazel
NDC 10733-801 · Medical Products Laboratories, Inc.
Key facts
| Product NDC | 10733-801 |
|---|---|
| Proprietary name | Witch Hazel |
| Nonproprietary name | Witch Hazel |
| Substances | WITCH HAZEL |
| Dosage form | LIQUID |
| Route | TOPICAL |
| Labeler | Medical Products Laboratories, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M015 |
| Marketing start | Jan 29, 2021 |
| 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: